Transcript: ENST00000464032.1 BPIFB1-203

Description

BPI fold containing family B member 1 [Source:HGNC Symbol;Acc:HGNC:16108]

Gene Synonyms

BA49G10.6, C20ORF114, DJ1187J4.1, LPLUNC1, MGC14597, VEMSGP

Location

Chromosome 20: 33,298,713-33,307,966 forward strand.

About this transcript

This transcript has 13 exons, is associated with 4377 variant alleles and maps to 369 oligo probes.

Gene

This transcript is a product of gene ENSG00000125999.11 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000253354.2	BPIFB1-201	1641	484aa	ENSP00000253354.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS13218	Q8TDL5-1	NM_033197.3	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000423645.5	BPIFB1-202	658	147aa	ENSP00000390471.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A2A2R0	-	TSL 3: A transcript where the only support is from a single EST The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:3, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000464032.1	BPIFB1-203	1933	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,

Summary

Statistics

Exons: 13, Coding exons: 0, Transcript length: 1,933 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000464032.1

Type

Protein coding CDS not defined

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Transcript: ENST00000464032.1 BPIFB1-203

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Transcript: ENST00000464032.1 BPIFB1-203

Summary

About Us

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