Canonical Allele Identifier: CA1720888254

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729650T= , CM000669.2:g.81729650T=	GRCh38
NC_000007.13:g.81358966T= , CM000669.1:g.81358966T=	GRCh37
NC_000007.12:g.81196902T=	NCBI36
NG_016274.1:g.45487A=
NG_016274.2:g.45487A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.995A= MANE Select	ENSP00000222390.5:p.Gln332=
ENST00000457544.7:c.980A=	ENSP00000391238.2:p.Gln327=
ENST00000222390.9:c.995A=	ENSP00000222390.5:p.Gln332=
ENST00000457544.6:c.980A=	ENSP00000391238.2:p.Gln327=
NM_000601.4:c.995A=	NP_000592.3:p.Gln332=
NM_001010932.1:c.980A=	NP_001010932.1:p.Gln327=
XM_006715956.2:c.995A=	XP_006716019.1:p.Gln332=
XM_011516115.1:c.980A=	XP_011514417.1:p.Gln327=
NM_000601.5:c.995A=	NP_000592.3:p.Gln332=
NM_001010932.2:c.980A=	NP_001010932.1:p.Gln327=
XM_011516115.2:c.980A=	XP_011514417.1:p.Gln327=
NM_000601.6:c.995A= MANE Select	NP_000592.3:p.Gln332=
NM_001010932.3:c.980A=	NP_001010932.1:p.Gln327=