Canonical Allele Identifier: CA1720888251

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729646A= , CM000669.2:g.81729646A=	GRCh38
NC_000007.13:g.81358962A= , CM000669.1:g.81358962A=	GRCh37
NC_000007.12:g.81196898A=	NCBI36
NG_016274.1:g.45491T=
NG_016274.2:g.45491T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.999T= MANE Select	ENSP00000222390.5:p.Tyr333=
ENST00000457544.7:c.984T=	ENSP00000391238.2:p.Tyr328=
ENST00000222390.9:c.999T=	ENSP00000222390.5:p.Tyr333=
ENST00000457544.6:c.984T=	ENSP00000391238.2:p.Tyr328=
NM_000601.4:c.999T=	NP_000592.3:p.Tyr333=
NM_001010932.1:c.984T=	NP_001010932.1:p.Tyr328=
XM_006715956.2:c.999T=	XP_006716019.1:p.Tyr333=
XM_011516115.1:c.984T=	XP_011514417.1:p.Tyr328=
NM_000601.5:c.999T=	NP_000592.3:p.Tyr333=
NM_001010932.2:c.984T=	NP_001010932.1:p.Tyr328=
XM_011516115.2:c.984T=	XP_011514417.1:p.Tyr328=
NM_000601.6:c.999T= MANE Select	NP_000592.3:p.Tyr333=
NM_001010932.3:c.984T=	NP_001010932.1:p.Tyr328=