Canonical Allele Identifier: CA1259613445

Gene: TGFA

Linked Data

• dbSNP Id: rs3771485

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70529159C>T , CM000664.2:g.70529159C>T	GRCh38
NC_000002.11:g.70756291C>T , CM000664.1:g.70756291C>T	GRCh37
NC_000002.10:g.70609799C>T	NCBI36
NG_029975.1:g.29857G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.41-14247G>A MANE Select	ENSP00000295400.6:n.41-14247G>A
ENST00000295400.10:c.41-14247G>A	ENSP00000295400.6:n.41-14247G>A
ENST00000394241.3:c.41-14247G>A	ENSP00000377787.3:n.41-14247G>A
ENST00000418333.6:c.41-14247G>A	ENSP00000404099.2:n.41-14247G>A
ENST00000444975.5:c.59-14247G>A	ENSP00000404131.1:n.59-14247G>A
ENST00000445399.5:c.41-14247G>A	ENSP00000387493.1:n.41-14247G>A
ENST00000450929.5:c.59-14247G>A	ENSP00000414127.1:n.59-14247G>A
ENST00000460808.5:n.100-14247G>A
ENST00000474101.1:n.94-14247G>A
NM_001099691.2:c.41-14247G>A	NP_001093161.1:n.41-14247G>A
NM_001308158.1:c.59-14247G>A	NP_001295087.1:n.59-14247G>A
NM_001308159.1:c.59-14247G>A	NP_001295088.1:n.59-14247G>A
NM_003236.3:c.41-14247G>A	NP_003227.1:n.41-14247G>A
NM_003236.4:c.41-14247G>A MANE Select	NP_003227.1:n.41-14247G>A
NM_001099691.3:c.41-14247G>A	NP_001093161.1:n.41-14247G>A
NM_001308158.2:c.59-14247G>A	NP_001295087.1:n.59-14247G>A
NM_001308159.2:c.59-14247G>A	NP_001295088.1:n.59-14247G>A