Human (GRCh38.p14)
Description

ess-2 splicing factor homolog [Source:HGNC Symbol;Acc:HGNC:16817]

Gene Synonyms

BIS1, DGCR13, DGCR14, DGS-H, DGSI, ES2, ES2EL, ESS-2

Location
About this transcript

This transcript has 10 exons, is annotated with 15 domains and features, is associated with 7570 variant alleles and maps to 711 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000252137.11ESS2-2015359476aaENSP00000252137.6
 
Protein coding
CCDS13756Q96DF8 NM_022719.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000434568.5ESS2-2021808293aaENSP00000388524.1
 
Nonsense mediated decay
F8WEF8 -TSL:5
ENST00000472073.1ESS2-2042101No protein-
 
Retained intron
--TSL:5
ENST00000469466.1ESS2-203581No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 10, Coding exons: 10, Transcript length: 5,359 bps, Translation length: 476 residues

MANE

This MANE Select transcript contains ENSP00000252137 and matches to NM_022719.3 and NP_073210.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96DF8

CCDS

This transcript is a member of the Human CCDS set: CCDS13756

Transcript Support Level (TSL)

TSL:1

Version

ENST00000252137.11

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.

GENCODE basic gene

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