Canonical Allele Identifier: CA1720888239

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729608C= , CM000669.2:g.81729608C=	GRCh38
NC_000007.13:g.81358924C= , CM000669.1:g.81358924C=	GRCh37
NC_000007.12:g.81196860C=	NCBI36
NG_016274.1:g.45529G=
NG_016274.2:g.45529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1037G= MANE Select	ENSP00000222390.5:p.Cys346=
ENST00000457544.7:c.1022G=	ENSP00000391238.2:p.Cys341=
ENST00000222390.9:c.1037G=	ENSP00000222390.5:p.Cys346=
ENST00000457544.6:c.1022G=	ENSP00000391238.2:p.Cys341=
NM_000601.4:c.1037G=	NP_000592.3:p.Cys346=
NM_001010932.1:c.1022G=	NP_001010932.1:p.Cys341=
XM_006715956.2:c.1037G=	XP_006716019.1:p.Cys346=
XM_011516115.1:c.1022G=	XP_011514417.1:p.Cys341=
NM_000601.5:c.1037G=	NP_000592.3:p.Cys346=
NM_001010932.2:c.1022G=	NP_001010932.1:p.Cys341=
XM_011516115.2:c.1022G=	XP_011514417.1:p.Cys341=
NM_000601.6:c.1037G= MANE Select	NP_000592.3:p.Cys346=
NM_001010932.3:c.1022G=	NP_001010932.1:p.Cys341=