Canonical Allele Identifier: CA182219

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81705509C>T , CM000669.2:g.81705509C>T	GRCh38
NC_000007.13:g.81334825C>T , CM000669.1:g.81334825C>T	GRCh37
NC_000007.12:g.81172761C>T	NCBI36
NG_016274.1:g.69628G>A
NG_016274.2:g.69628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1891G>A MANE Select	ENSP00000222390.5:p.Val631Met
ENST00000457544.7:c.1876G>A	ENSP00000391238.2:p.Val626Met
ENST00000222390.9:c.1891G>A	ENSP00000222390.5:p.Val631Met
ENST00000457544.6:c.1876G>A	ENSP00000391238.2:p.Val626Met
NM_000601.4:c.1891G>A	NP_000592.3:p.Val631Met
NM_001010932.1:c.1876G>A	NP_001010932.1:p.Val626Met
XM_006715956.2:c.1891G>A	XP_006716019.1:p.Val631Met
XM_011516115.1:c.1876G>A	XP_011514417.1:p.Val626Met
NM_000601.5:c.1891G>A	NP_000592.3:p.Val631Met
NM_001010932.2:c.1876G>A	NP_001010932.1:p.Val626Met
XM_011516115.2:c.1876G>A	XP_011514417.1:p.Val626Met
NM_000601.6:c.1891G>A MANE Select	NP_000592.3:p.Val631Met
NM_001010932.3:c.1876G>A	NP_001010932.1:p.Val626Met