Canonical Allele Identifier: CA1720888229

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729585C= , CM000669.2:g.81729585C=	GRCh38
NC_000007.13:g.81358901C= , CM000669.1:g.81358901C=	GRCh37
NC_000007.12:g.81196837C=	NCBI36
NG_016274.1:g.45552G=
NG_016274.2:g.45552G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1040+20G= MANE Select	ENSP00000222390.5:n.1040+20G=
ENST00000457544.7:c.1025+20G=	ENSP00000391238.2:n.1025+20G=
ENST00000222390.9:c.1040+20G=	ENSP00000222390.5:n.1040+20G=
ENST00000457544.6:c.1025+20G=	ENSP00000391238.2:n.1025+20G=
NM_000601.4:c.1040+20G=	NP_000592.3:n.1040+20G=
NM_001010932.1:c.1025+20G=	NP_001010932.1:n.1025+20G=
XM_006715956.2:c.1040+20G=	XP_006716019.1:n.1040+20G=
XM_011516115.1:c.1025+20G=	XP_011514417.1:n.1025+20G=
NM_000601.5:c.1040+20G=	NP_000592.3:n.1040+20G=
NM_001010932.2:c.1025+20G=	NP_001010932.1:n.1025+20G=
XM_011516115.2:c.1025+20G=	XP_011514417.1:n.1025+20G=
NM_000601.6:c.1040+20G= MANE Select	NP_000592.3:n.1040+20G=
NM_001010932.3:c.1025+20G=	NP_001010932.1:n.1025+20G=