Canonical Allele Identifier: CA1720888237

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729598T= , CM000669.2:g.81729598T=	GRCh38
NC_000007.13:g.81358914T= , CM000669.1:g.81358914T=	GRCh37
NC_000007.12:g.81196850T=	NCBI36
NG_016274.1:g.45539A=
NG_016274.2:g.45539A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1040+7A= MANE Select	ENSP00000222390.5:n.1040+7A=
ENST00000457544.7:c.1025+7A=	ENSP00000391238.2:n.1025+7A=
ENST00000222390.9:c.1040+7A=	ENSP00000222390.5:n.1040+7A=
ENST00000457544.6:c.1025+7A=	ENSP00000391238.2:n.1025+7A=
NM_000601.4:c.1040+7A=	NP_000592.3:n.1040+7A=
NM_001010932.1:c.1025+7A=	NP_001010932.1:n.1025+7A=
XM_006715956.2:c.1040+7A=	XP_006716019.1:n.1040+7A=
XM_011516115.1:c.1025+7A=	XP_011514417.1:n.1025+7A=
NM_000601.5:c.1040+7A=	NP_000592.3:n.1040+7A=
NM_001010932.2:c.1025+7A=	NP_001010932.1:n.1025+7A=
XM_011516115.2:c.1025+7A=	XP_011514417.1:n.1025+7A=
NM_000601.6:c.1040+7A= MANE Select	NP_000592.3:n.1040+7A=
NM_001010932.3:c.1025+7A=	NP_001010932.1:n.1025+7A=