Canonical Allele Identifier: CA367871201

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81359060C>G (hg19) ; chr7:g.81729744C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729744C>G , CM000669.2:g.81729744C>G	GRCh38
NC_000007.13:g.81359060C>G , CM000669.1:g.81359060C>G	GRCh37
NC_000007.12:g.81196996C>G	NCBI36
NG_016274.1:g.45393G>C
NG_016274.2:g.45393G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.901G>C MANE Select	ENSP00000222390.5:p.Glu301Gln
ENST00000457544.7:c.886G>C	ENSP00000391238.2:p.Glu296Gln
ENST00000222390.9:c.901G>C	ENSP00000222390.5:p.Glu301Gln
ENST00000457544.6:c.886G>C	ENSP00000391238.2:p.Glu296Gln
NM_000601.4:c.901G>C	NP_000592.3:p.Glu301Gln
NM_001010932.1:c.886G>C	NP_001010932.1:p.Glu296Gln
XM_006715956.2:c.901G>C	XP_006716019.1:p.Glu301Gln
XM_011516115.1:c.886G>C	XP_011514417.1:p.Glu296Gln
NM_000601.5:c.901G>C	NP_000592.3:p.Glu301Gln
NM_001010932.2:c.886G>C	NP_001010932.1:p.Glu296Gln
XM_011516115.2:c.886G>C	XP_011514417.1:p.Glu296Gln
NM_000601.6:c.901G>C MANE Select	NP_000592.3:p.Glu301Gln
NM_001010932.3:c.886G>C	NP_001010932.1:p.Glu296Gln