Canonical Allele Identifier: CA367872553

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81705701A>G , CM000669.2:g.81705701A>G	GRCh38
NC_000007.13:g.81335017A>G , CM000669.1:g.81335017A>G	GRCh37
NC_000007.12:g.81172953A>G	NCBI36
NG_016274.1:g.69436T>C
NG_016274.2:g.69436T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1810T>C MANE Select	ENSP00000222390.5:p.Cys604Arg
ENST00000457544.7:c.1795T>C	ENSP00000391238.2:p.Cys599Arg
ENST00000222390.9:c.1810T>C	ENSP00000222390.5:p.Cys604Arg
ENST00000457544.6:c.1795T>C	ENSP00000391238.2:p.Cys599Arg
NM_000601.4:c.1810T>C	NP_000592.3:p.Cys604Arg
NM_001010932.1:c.1795T>C	NP_001010932.1:p.Cys599Arg
XM_006715956.2:c.1810T>C	XP_006716019.1:p.Cys604Arg
XM_011516115.1:c.1795T>C	XP_011514417.1:p.Cys599Arg
NM_000601.5:c.1810T>C	NP_000592.3:p.Cys604Arg
NM_001010932.2:c.1795T>C	NP_001010932.1:p.Cys599Arg
XM_011516115.2:c.1795T>C	XP_011514417.1:p.Cys599Arg
NM_000601.6:c.1810T>C MANE Select	NP_000592.3:p.Cys604Arg
NM_001010932.3:c.1795T>C	NP_001010932.1:p.Cys599Arg