Canonical Allele Identifier: CA1720888248

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729640G= , CM000669.2:g.81729640G=	GRCh38
NC_000007.13:g.81358956G= , CM000669.1:g.81358956G=	GRCh37
NC_000007.12:g.81196892G=	NCBI36
NG_016274.1:g.45497C=
NG_016274.2:g.45497C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1005C= MANE Select	ENSP00000222390.5:p.His335=
ENST00000457544.7:c.990C=	ENSP00000391238.2:p.His330=
ENST00000222390.9:c.1005C=	ENSP00000222390.5:p.His335=
ENST00000457544.6:c.990C=	ENSP00000391238.2:p.His330=
NM_000601.4:c.1005C=	NP_000592.3:p.His335=
NM_001010932.1:c.990C=	NP_001010932.1:p.His330=
XM_006715956.2:c.1005C=	XP_006716019.1:p.His335=
XM_011516115.1:c.990C=	XP_011514417.1:p.His330=
NM_000601.5:c.1005C=	NP_000592.3:p.His335=
NM_001010932.2:c.990C=	NP_001010932.1:p.His330=
XM_011516115.2:c.990C=	XP_011514417.1:p.His330=
NM_000601.6:c.1005C= MANE Select	NP_000592.3:p.His335=
NM_001010932.3:c.990C=	NP_001010932.1:p.His330=