Canonical Allele Identifier: CA367869958

Gene: HGF

Linked Data

• gnomAD v4: 7-81725940-C-G
• MyVariant Identifiers: chr7:g.81355256C>G (hg19) ; chr7:g.81725940C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725940C>G , CM000669.2:g.81725940C>G	GRCh38
NC_000007.13:g.81355256C>G , CM000669.1:g.81355256C>G	GRCh37
NC_000007.12:g.81193192C>G	NCBI36
NG_016274.1:g.49197G>C
NG_016274.2:g.49197G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1118G>C MANE Select	ENSP00000222390.5:p.Arg373Pro
ENST00000457544.7:c.1103G>C	ENSP00000391238.2:p.Arg368Pro
ENST00000222390.9:c.1118G>C	ENSP00000222390.5:p.Arg373Pro
ENST00000457544.6:c.1103G>C	ENSP00000391238.2:p.Arg368Pro
NM_000601.4:c.1118G>C	NP_000592.3:p.Arg373Pro
NM_001010932.1:c.1103G>C	NP_001010932.1:p.Arg368Pro
XM_006715956.2:c.1118G>C	XP_006716019.1:p.Arg373Pro
XM_011516115.1:c.1103G>C	XP_011514417.1:p.Arg368Pro
NM_000601.5:c.1118G>C	NP_000592.3:p.Arg373Pro
NM_001010932.2:c.1103G>C	NP_001010932.1:p.Arg368Pro
XM_011516115.2:c.1103G>C	XP_011514417.1:p.Arg368Pro
NM_000601.6:c.1118G>C MANE Select	NP_000592.3:p.Arg373Pro
NM_001010932.3:c.1103G>C	NP_001010932.1:p.Arg368Pro