Human (GRCh38.p14)
Description

cell death inducing DFFA like effector b [Source:HGNC Symbol;Acc:HGNC:1977]

Location
About this transcript

This transcript has 7 exons, is annotated with 10 domains and features, is associated with 3283 variant alleles and maps to 392 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000554411.6CIDEB-2031225219aaENSP00000451089.1
 
Protein coding
CCDS32056Q9UHD4 NM_001393339.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000336557.9CIDEB-2022409219aaENSP00000337731.5
 
Protein coding
CCDS32056Q9UHD4 -GENCODE basicAPPRIS P1TSL:2
ENST00000258807.5CIDEB-2012294219aaENSP00000258807.5
 
Protein coding
CCDS32056Q9UHD4 -GENCODE basicAPPRIS P1TSL:1
ENST00000556756.1CIDEB-20624861aaENSP00000451744.2
 
Protein coding
G3V4E2 -TSL:5CDS 5' incomplete
ENST00000555817.1CIDEB-205552No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000555471.1CIDEB-204532No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 7, Coding exons: 5, Transcript length: 2,294 bps, Translation length: 219 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UHD4

CCDS

This transcript is a member of the Human CCDS set: CCDS32056

Transcript Support Level (TSL)

TSL:1

Version

ENST00000258807.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Annotation Attributes

dotter confirmed [Definitions]

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.