Human (GRCh38.p14)
Description

ELL associated factor 1 [Source:HGNC Symbol;Acc:HGNC:20907]

Location

Chromosome 3: 15,427,598-15,450,635 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 3 transcripts (splice variants), 209 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000396842.7EAF1-2014447268aaENSP00000380054.2
 
Protein coding
CCDS2626Q96JC9-1 NM_033083.7MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000449565.1EAF1-202103767aaENSP00000399636.1
 
Nonsense mediated decay
F8WFA5 -TSL:2
ENST00000617675.1EAF1-203556No protein-
 
Protein coding CDS not defined
--TSL:4