Canonical Allele Identifier: CA1259574399

Gene: TGFA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450862G= , CM000664.2:g.70450862G=	GRCh38
NC_000002.11:g.70677994G= , CM000664.1:g.70677994G=	GRCh37
NC_000002.10:g.70531502G=	NCBI36
NG_029975.1:g.108154C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295400.11:c.480C= MANE Select	ENSP00000295400.6:p.Val160=
ENST00000295400.10:c.480C=	ENSP00000295400.6:p.Val160=
ENST00000418333.6:c.477C=	ENSP00000404099.2:p.Val159=
ENST00000419940.5:c.379-1241C=
ENST00000444975.5:c.498C=	ENSP00000404131.1:p.Val166=
ENST00000445399.5:c.*18+867C=	ENSP00000387493.1:n.*18+867C=
ENST00000450929.5:c.495C=	ENSP00000414127.1:p.Val165=
NM_001099691.2:c.477C=	NP_001093161.1:p.Val159=
NM_001308158.1:c.498C=	NP_001295087.1:p.Val166=
NM_001308159.1:c.495C=	NP_001295088.1:p.Val165=
NM_003236.3:c.480C=	NP_003227.1:p.Val160=
NM_003236.4:c.480C= MANE Select	NP_003227.1:p.Val160=
NM_001099691.3:c.477C=	NP_001093161.1:p.Val159=
NM_001308158.2:c.498C=	NP_001295087.1:p.Val166=
NM_001308159.2:c.495C=	NP_001295088.1:p.Val165=