Canonical Allele Identifier: CA2580077377

Gene: HGF

Linked Data

• ClinVar Variation Id: 2066301
• ClinVar RCV Id: RCV002966110
• dbSNP Id: rs1584002170

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81757184C>G , CM000669.2:g.81757184C>G	GRCh38
NC_000007.13:g.81386500C>G , CM000669.1:g.81386500C>G	GRCh37
NC_000007.12:g.81224436C>G	NCBI36
NG_016274.1:g.17953G>C
NG_016274.2:g.17953G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.482+5G>C MANE Select	ENSP00000222390.5:n.482+5G>C
ENST00000423064.7:c.482+5G>C	ENSP00000413829.2:n.482+5G>C
ENST00000444829.7:c.482+5G>C	ENSP00000389854.2:n.482+5G>C
ENST00000453411.6:c.482+5G>C	ENSP00000408270.1:n.482+5G>C
ENST00000457544.7:c.482+5G>C	ENSP00000391238.2:n.482+5G>C
ENST00000465234.2:c.482+5G>C	ENSP00000494355.1:n.482+5G>C
ENST00000643024.1:c.487G>C	ENSP00000496217.1:n.487G>C
ENST00000222390.9:c.482+5G>C	ENSP00000222390.5:n.482+5G>C
ENST00000354224.10:c.482+5G>C	ENSP00000346164.6:n.482+5G>C
ENST00000423064.6:c.482+5G>C	ENSP00000413829.2:n.482+5G>C
ENST00000444829.6:c.482+5G>C	ENSP00000389854.2:n.482+5G>C
ENST00000453018.1:c.*1G>C	ENSP00000395468.1:n.*1G>C
ENST00000453411.5:c.482+5G>C	ENSP00000408270.1:n.482+5G>C
ENST00000457544.6:c.482+5G>C	ENSP00000391238.2:n.482+5G>C
ENST00000465234.1:n.510+5G>C
NM_000601.4:c.482+5G>C	NP_000592.3:n.482+5G>C
NM_001010931.1:c.482+5G>C	NP_001010931.1:n.482+5G>C
NM_001010931.2:c.482+5G>C	NP_001010931.1:n.482+5G>C
NM_001010932.1:c.482+5G>C	NP_001010932.1:n.482+5G>C
NM_001010933.1:c.482+5G>C	NP_001010933.1:n.482+5G>C
NM_001010933.2:c.482+5G>C	NP_001010933.1:n.482+5G>C
NM_001010934.1:c.482+5G>C	NP_001010934.1:n.482+5G>C
NM_001010934.2:c.482+5G>C	NP_001010934.1:n.482+5G>C
XM_006715956.2:c.482+5G>C	XP_006716019.1:n.482+5G>C
XM_011516115.1:c.482+5G>C	XP_011514417.1:n.482+5G>C
NM_000601.5:c.482+5G>C	NP_000592.3:n.482+5G>C
NM_001010932.2:c.482+5G>C	NP_001010932.1:n.482+5G>C
XM_011516115.2:c.482+5G>C	XP_011514417.1:n.482+5G>C
XM_017012097.1:c.482+5G>C	XP_016867586.1:n.482+5G>C
XM_017012098.1:c.482+5G>C	XP_016867587.1:n.482+5G>C
NM_000601.6:c.482+5G>C MANE Select	NP_000592.3:n.482+5G>C
NM_001010931.3:c.482+5G>C	NP_001010931.1:n.482+5G>C
NM_001010932.3:c.482+5G>C	NP_001010932.1:n.482+5G>C
NM_001010933.3:c.482+5G>C	NP_001010933.1:n.482+5G>C
NM_001010934.3:c.482+5G>C	NP_001010934.1:n.482+5G>C