Canonical Allele Identifier: CA1720885403

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81752157T= , CM000669.2:g.81752157T=	GRCh38
NC_000007.13:g.81381473T= , CM000669.1:g.81381473T=	GRCh37
NC_000007.12:g.81219409T=	NCBI36
NG_016274.1:g.22980A=
NG_016274.2:g.22980A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.588A= MANE Select	ENSP00000222390.5:p.Val196=
ENST00000423064.7:c.588A=	ENSP00000413829.2:p.Val196=
ENST00000444829.7:c.588A=	ENSP00000389854.2:p.Val196=
ENST00000453411.6:c.573A=	ENSP00000408270.1:p.Val191=
ENST00000457544.7:c.573A=	ENSP00000391238.2:p.Val191=
ENST00000465234.2:c.573A=	ENSP00000494355.1:p.Val191=
ENST00000222390.9:c.588A=	ENSP00000222390.5:p.Val196=
ENST00000423064.6:c.588A=	ENSP00000413829.2:p.Val196=
ENST00000444829.6:c.588A=	ENSP00000389854.2:p.Val196=
ENST00000453411.5:c.573A=	ENSP00000408270.1:p.Val191=
ENST00000457544.6:c.573A=	ENSP00000391238.2:p.Val191=
ENST00000465234.1:n.601A=
NM_000601.4:c.588A=	NP_000592.3:p.Val196=
NM_001010931.1:c.588A=	NP_001010931.1:p.Val196=
NM_001010931.2:c.588A=	NP_001010931.1:p.Val196=
NM_001010932.1:c.573A=	NP_001010932.1:p.Val191=
NM_001010933.1:c.573A=	NP_001010933.1:p.Val191=
NM_001010933.2:c.573A=	NP_001010933.1:p.Val191=
NM_001010934.1:c.588A=	NP_001010934.1:p.Val196=
NM_001010934.2:c.588A=	NP_001010934.1:p.Val196=
XM_006715956.2:c.588A=	XP_006716019.1:p.Val196=
XM_011516115.1:c.573A=	XP_011514417.1:p.Val191=
NM_000601.5:c.588A=	NP_000592.3:p.Val196=
NM_001010932.2:c.573A=	NP_001010932.1:p.Val191=
XM_011516115.2:c.573A=	XP_011514417.1:p.Val191=
XM_017012097.1:c.588A=	XP_016867586.1:p.Val196=
XM_017012098.1:c.573A=	XP_016867587.1:p.Val191=
NM_000601.6:c.588A= MANE Select	NP_000592.3:p.Val196=
NM_001010931.3:c.588A=	NP_001010931.1:p.Val196=
NM_001010932.3:c.573A=	NP_001010932.1:p.Val191=
NM_001010933.3:c.573A=	NP_001010933.1:p.Val191=
NM_001010934.3:c.588A=	NP_001010934.1:p.Val196=