Canonical Allele Identifier: CA367870761

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81358944C>G (hg19) ; chr7:g.81729628C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729628C>G , CM000669.2:g.81729628C>G	GRCh38
NC_000007.13:g.81358944C>G , CM000669.1:g.81358944C>G	GRCh37
NC_000007.12:g.81196880C>G	NCBI36
NG_016274.1:g.45509G>C
NG_016274.2:g.45509G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1017G>C MANE Select	ENSP00000222390.5:p.Met339Ile
ENST00000457544.7:c.1002G>C	ENSP00000391238.2:p.Met334Ile
ENST00000222390.9:c.1017G>C	ENSP00000222390.5:p.Met339Ile
ENST00000457544.6:c.1002G>C	ENSP00000391238.2:p.Met334Ile
NM_000601.4:c.1017G>C	NP_000592.3:p.Met339Ile
NM_001010932.1:c.1002G>C	NP_001010932.1:p.Met334Ile
XM_006715956.2:c.1017G>C	XP_006716019.1:p.Met339Ile
XM_011516115.1:c.1002G>C	XP_011514417.1:p.Met334Ile
NM_000601.5:c.1017G>C	NP_000592.3:p.Met339Ile
NM_001010932.2:c.1002G>C	NP_001010932.1:p.Met334Ile
XM_011516115.2:c.1002G>C	XP_011514417.1:p.Met334Ile
NM_000601.6:c.1017G>C MANE Select	NP_000592.3:p.Met339Ile
NM_001010932.3:c.1002G>C	NP_001010932.1:p.Met334Ile