Canonical Allele Identifier: CA367870775

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81358949C>G (hg19) ; chr7:g.81729633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729633C>G , CM000669.2:g.81729633C>G	GRCh38
NC_000007.13:g.81358949C>G , CM000669.1:g.81358949C>G	GRCh37
NC_000007.12:g.81196885C>G	NCBI36
NG_016274.1:g.45504G>C
NG_016274.2:g.45504G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1012G>C MANE Select	ENSP00000222390.5:p.Asp338His
ENST00000457544.7:c.997G>C	ENSP00000391238.2:p.Asp333His
ENST00000222390.9:c.1012G>C	ENSP00000222390.5:p.Asp338His
ENST00000457544.6:c.997G>C	ENSP00000391238.2:p.Asp333His
NM_000601.4:c.1012G>C	NP_000592.3:p.Asp338His
NM_001010932.1:c.997G>C	NP_001010932.1:p.Asp333His
XM_006715956.2:c.1012G>C	XP_006716019.1:p.Asp338His
XM_011516115.1:c.997G>C	XP_011514417.1:p.Asp333His
NM_000601.5:c.1012G>C	NP_000592.3:p.Asp338His
NM_001010932.2:c.997G>C	NP_001010932.1:p.Asp333His
XM_011516115.2:c.997G>C	XP_011514417.1:p.Asp333His
NM_000601.6:c.1012G>C MANE Select	NP_000592.3:p.Asp338His
NM_001010932.3:c.997G>C	NP_001010932.1:p.Asp333His