Canonical Allele Identifier: CA367873489

Gene: HGF

Linked Data

• gnomAD v4: 7-81711517-C-T
• MyVariant Identifiers: chr7:g.81340833C>T (hg19) ; chr7:g.81711517C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81711517C>T , CM000669.2:g.81711517C>T	GRCh38
NC_000007.13:g.81340833C>T , CM000669.1:g.81340833C>T	GRCh37
NC_000007.12:g.81178769C>T	NCBI36
NG_016274.1:g.63620G>A
NG_016274.2:g.63620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1408G>A MANE Select	ENSP00000222390.5:p.Glu470Lys
ENST00000457544.7:c.1393G>A	ENSP00000391238.2:p.Glu465Lys
ENST00000222390.9:c.1408G>A	ENSP00000222390.5:p.Glu470Lys
ENST00000457544.6:c.1393G>A	ENSP00000391238.2:p.Glu465Lys
NM_000601.4:c.1408G>A	NP_000592.3:p.Glu470Lys
NM_001010932.1:c.1393G>A	NP_001010932.1:p.Glu465Lys
XM_006715956.2:c.1408G>A	XP_006716019.1:p.Glu470Lys
XM_011516115.1:c.1393G>A	XP_011514417.1:p.Glu465Lys
NM_000601.5:c.1408G>A	NP_000592.3:p.Glu470Lys
NM_001010932.2:c.1393G>A	NP_001010932.1:p.Glu465Lys
XM_011516115.2:c.1393G>A	XP_011514417.1:p.Glu465Lys
NM_000601.6:c.1408G>A MANE Select	NP_000592.3:p.Glu470Lys
NM_001010932.3:c.1393G>A	NP_001010932.1:p.Glu465Lys