Canonical Allele Identifier: CA1259573996

Gene: TGFA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450323T= , CM000664.2:g.70450323T=	GRCh38
NC_000002.11:g.70677455T= , CM000664.1:g.70677455T=	GRCh37
NC_000002.10:g.70530963T=	NCBI36
NG_029975.1:g.108693A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*536A= MANE Select	ENSP00000295400.6:n.*536A=
ENST00000295400.10:c.*536A=	ENSP00000295400.6:n.*536A=
ENST00000418333.6:c.*536A=	ENSP00000404099.2:n.*536A=
ENST00000419940.5:c.379-702A=
ENST00000445399.5:c.*19-702A=	ENSP00000387493.1:n.*19-702A=
NM_001099691.2:c.*536A=	NP_001093161.1:n.*536A=
NM_001308158.1:c.*536A=	NP_001295087.1:n.*536A=
NM_001308159.1:c.*536A=	NP_001295088.1:n.*536A=
NM_003236.3:c.*536A=	NP_003227.1:n.*536A=
NM_003236.4:c.*536A= MANE Select	NP_003227.1:n.*536A=
NM_001099691.3:c.*536A=	NP_001093161.1:n.*536A=
NM_001308158.2:c.*536A=	NP_001295087.1:n.*536A=
NM_001308159.2:c.*536A=	NP_001295088.1:n.*536A=