Transcript: ENST00000672739.1

Description

novel protein, HAUS3-POLN readthrough

Location

About this transcript

This transcript has 27 exons, is annotated with 8 domains and features, is associated with 72093 variant alleles and maps to 1057 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000672725.1	-	4600	935aa	ENSP00000500518.1	Nonsense mediated decay		A0A5F9ZHQ7	-	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,
ENST00000672739.1	-	5738	603aa	ENSP00000500512.1	Nonsense mediated decay	CCDS33941	-	-	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,

Summary

Statistics

Exons: 27, Coding exons: 4, Transcript length: 5,738 bps, Translation length: 603 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS33941

Version

ENST00000672739.1

Type

Nonsense mediated decay

Annotation Method

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

Annotation Attributes

RNA-Seq supported only [Definitions]