Canonical Allele Identifier: CA176276

Gene: HGF

Linked Data

• ClinVar Variation Id: 163660
• ClinVar RCV Id: RCV000150806 ; RCV000477953
• dbSNP Id: rs374484762
• MyVariant Identifiers: chr7:g.81358978C>A (hg19) ; chr7:g.81729662C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729662C>A , CM000669.2:g.81729662C>A	GRCh38
NC_000007.13:g.81358978C>A , CM000669.1:g.81358978C>A	GRCh37
NC_000007.12:g.81196914C>A	NCBI36
NG_016274.1:g.45475G>T
NG_016274.2:g.45475G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.983G>T MANE Select	ENSP00000222390.5:p.Arg328Leu
ENST00000457544.7:c.968G>T	ENSP00000391238.2:p.Arg323Leu
ENST00000222390.9:c.983G>T	ENSP00000222390.5:p.Arg328Leu
ENST00000457544.6:c.968G>T	ENSP00000391238.2:p.Arg323Leu
NM_000601.4:c.983G>T	NP_000592.3:p.Arg328Leu
NM_001010932.1:c.968G>T	NP_001010932.1:p.Arg323Leu
XM_006715956.2:c.983G>T	XP_006716019.1:p.Arg328Leu
XM_011516115.1:c.968G>T	XP_011514417.1:p.Arg323Leu
NM_000601.5:c.983G>T	NP_000592.3:p.Arg328Leu
NM_001010932.2:c.968G>T	NP_001010932.1:p.Arg323Leu
XM_011516115.2:c.968G>T	XP_011514417.1:p.Arg323Leu
NM_000601.6:c.983G>T MANE Select	NP_000592.3:p.Arg328Leu
NM_001010932.3:c.968G>T	NP_001010932.1:p.Arg323Leu