Canonical Allele Identifier: CA367870006

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81355278A>C (hg19) ; chr7:g.81725962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725962A>C , CM000669.2:g.81725962A>C	GRCh38
NC_000007.13:g.81355278A>C , CM000669.1:g.81355278A>C	GRCh37
NC_000007.12:g.81193214A>C	NCBI36
NG_016274.1:g.49175T>G
NG_016274.2:g.49175T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1096T>G MANE Select	ENSP00000222390.5:p.Phe366Val
ENST00000457544.7:c.1081T>G	ENSP00000391238.2:p.Phe361Val
ENST00000222390.9:c.1096T>G	ENSP00000222390.5:p.Phe366Val
ENST00000457544.6:c.1081T>G	ENSP00000391238.2:p.Phe361Val
NM_000601.4:c.1096T>G	NP_000592.3:p.Phe366Val
NM_001010932.1:c.1081T>G	NP_001010932.1:p.Phe361Val
XM_006715956.2:c.1096T>G	XP_006716019.1:p.Phe366Val
XM_011516115.1:c.1081T>G	XP_011514417.1:p.Phe361Val
NM_000601.5:c.1096T>G	NP_000592.3:p.Phe366Val
NM_001010932.2:c.1081T>G	NP_001010932.1:p.Phe361Val
XM_011516115.2:c.1081T>G	XP_011514417.1:p.Phe361Val
NM_000601.6:c.1096T>G MANE Select	NP_000592.3:p.Phe366Val
NM_001010932.3:c.1081T>G	NP_001010932.1:p.Phe361Val