Canonical Allele Identifier: CA161107834

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81706359T>C , CM000669.2:g.81706359T>C	GRCh38
NC_000007.13:g.81335675T>C , CM000669.1:g.81335675T>C	GRCh37
NC_000007.12:g.81173611T>C	NCBI36
NG_016274.1:g.68778A>G
NG_016274.2:g.68778A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000601.6:c.1685A>G MANE Select	NP_000592.3:p.Lys562Arg
ENST00000222390.11:c.1685A>G MANE Select	ENSP00000222390.5:p.Lys562Arg
NM_000601.4:c.1685A>G	NP_000592.3:p.Lys562Arg
NM_000601.5:c.1685A>G	NP_000592.3:p.Lys562Arg
NM_001010932.1:c.1670A>G	NP_001010932.1:p.Lys557Arg
NM_001010932.2:c.1670A>G	NP_001010932.1:p.Lys557Arg
NM_001010932.3:c.1670A>G	NP_001010932.1:p.Lys557Arg
ENST00000222390.9:c.1685A>G	ENSP00000222390.5:p.Lys562Arg
ENST00000457544.6:c.1670A>G	ENSP00000391238.2:p.Lys557Arg
ENST00000457544.7:c.1670A>G	ENSP00000391238.2:p.Lys557Arg
XM_006715956.2:c.1685A>G	XP_006716019.1:p.Lys562Arg
XM_011516115.1:c.1670A>G	XP_011514417.1:p.Lys557Arg
XM_011516115.2:c.1670A>G	XP_011514417.1:p.Lys557Arg