Human (GRCh38.p14)
Description

transforming growth factor alpha [Source:HGNC Symbol;Acc:HGNC:11765]

Location

Chromosome 2: 70,447,284-70,554,193 reverse strand.

GRCh38:CM000664.2

About this gene

This gene has 9 transcripts (splice variants), 190 orthologues, 5 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000295400.11TGFA-2014117160aaENSP00000295400.6
 
Protein coding
CCDS1905P01135-1 NM_003236.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000418333.6TGFA-2031225159aaENSP00000404099.2
 
Protein coding
CCDS46316P01135-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000444975.5TGFA-205985166aaENSP00000404131.1
 
Protein coding
CCDS77420F8VNR3 -GENCODE basicTSL:1
ENST00000450929.5TGFA-207950165aaENSP00000414127.1
 
Protein coding
CCDS77419E7EPT6 -GENCODE basicTSL:1
ENST00000445399.5TGFA-206812161aaENSP00000387493.1
 
Protein coding
P01135-3 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000419940.5TGFA-204681131aaENSP00000407432.1
 
Protein coding
H0Y6S5 -TSL:5CDS 5' incomplete
ENST00000394241.3TGFA-202568120aaENSP00000377787.3
 
Protein coding
F8WA74 -TSL:3CDS 3' incomplete
ENST00000460808.5TGFA-208470No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000474101.1TGFA-209147No protein-
 
Protein coding CDS not defined
--TSL:5