Canonical Allele Identifier: CA367871210

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81359065G>C (hg19) ; chr7:g.81729749G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729749G>C , CM000669.2:g.81729749G>C	GRCh38
NC_000007.13:g.81359065G>C , CM000669.1:g.81359065G>C	GRCh37
NC_000007.12:g.81197001G>C	NCBI36
NG_016274.1:g.45388C>G
NG_016274.2:g.45388C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.896C>G MANE Select	ENSP00000222390.5:p.Pro299Arg
ENST00000457544.7:c.881C>G	ENSP00000391238.2:p.Pro294Arg
ENST00000222390.9:c.896C>G	ENSP00000222390.5:p.Pro299Arg
ENST00000457544.6:c.881C>G	ENSP00000391238.2:p.Pro294Arg
NM_000601.4:c.896C>G	NP_000592.3:p.Pro299Arg
NM_001010932.1:c.881C>G	NP_001010932.1:p.Pro294Arg
XM_006715956.2:c.896C>G	XP_006716019.1:p.Pro299Arg
XM_011516115.1:c.881C>G	XP_011514417.1:p.Pro294Arg
NM_000601.5:c.896C>G	NP_000592.3:p.Pro299Arg
NM_001010932.2:c.881C>G	NP_001010932.1:p.Pro294Arg
XM_011516115.2:c.881C>G	XP_011514417.1:p.Pro294Arg
NM_000601.6:c.896C>G MANE Select	NP_000592.3:p.Pro299Arg
NM_001010932.3:c.881C>G	NP_001010932.1:p.Pro294Arg