Human (GRCh38.p14)
Description

epsin 1 [Source:HGNC Symbol;Acc:HGNC:21604]

Location

Chromosome 19: 55,675,226-55,709,858 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 7 transcripts (splice variants), 255 orthologues and 5 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000270460.11EPN1-20216219576aaENSP00000270460.6
 
Protein coding
CCDS46199Q9Y6I3-2 NM_001130072.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P3TSL:2
ENST00000411543.6EPN1-2032621662aaENSP00000406209.1
 
Protein coding
CCDS46198Q9Y6I3-1 -GENCODE basicTSL:1
ENST00000085079.11EPN1-2012355550aaENSP00000085079.6
 
Protein coding
CCDS46200Q9Y6I3-3 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000589704.1EPN1-20625060aaENSP00000466593.2
 
Protein coding
K7EMP4 -TSL:5CDS 5' incomplete
ENST00000591743.1EPN1-207593No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000587937.1EPN1-205537No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000586194.1EPN1-204583No protein-
 
Retained intron
--TSL:2