Canonical Allele Identifier: CA367874778

Gene: HGF

Linked Data

• gnomAD v4: 7-81752158-A-G
• MyVariant Identifiers: chr7:g.81381474A>G (hg19) ; chr7:g.81752158A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81752158A>G , CM000669.2:g.81752158A>G	GRCh38
NC_000007.13:g.81381474A>G , CM000669.1:g.81381474A>G	GRCh37
NC_000007.12:g.81219410A>G	NCBI36
NG_016274.1:g.22979T>C
NG_016274.2:g.22979T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.587T>C MANE Select	ENSP00000222390.5:p.Val196Ala
ENST00000423064.7:c.587T>C	ENSP00000413829.2:p.Val196Ala
ENST00000444829.7:c.587T>C	ENSP00000389854.2:p.Val196Ala
ENST00000453411.6:c.572T>C	ENSP00000408270.1:p.Val191Ala
ENST00000457544.7:c.572T>C	ENSP00000391238.2:p.Val191Ala
ENST00000465234.2:c.572T>C	ENSP00000494355.1:p.Val191Ala
ENST00000222390.9:c.587T>C	ENSP00000222390.5:p.Val196Ala
ENST00000423064.6:c.587T>C	ENSP00000413829.2:p.Val196Ala
ENST00000444829.6:c.587T>C	ENSP00000389854.2:p.Val196Ala
ENST00000453411.5:c.572T>C	ENSP00000408270.1:p.Val191Ala
ENST00000457544.6:c.572T>C	ENSP00000391238.2:p.Val191Ala
ENST00000465234.1:n.600T>C
NM_000601.4:c.587T>C	NP_000592.3:p.Val196Ala
NM_001010931.1:c.587T>C	NP_001010931.1:p.Val196Ala
NM_001010931.2:c.587T>C	NP_001010931.1:p.Val196Ala
NM_001010932.1:c.572T>C	NP_001010932.1:p.Val191Ala
NM_001010933.1:c.572T>C	NP_001010933.1:p.Val191Ala
NM_001010933.2:c.572T>C	NP_001010933.1:p.Val191Ala
NM_001010934.1:c.587T>C	NP_001010934.1:p.Val196Ala
NM_001010934.2:c.587T>C	NP_001010934.1:p.Val196Ala
XM_006715956.2:c.587T>C	XP_006716019.1:p.Val196Ala
XM_011516115.1:c.572T>C	XP_011514417.1:p.Val191Ala
NM_000601.5:c.587T>C	NP_000592.3:p.Val196Ala
NM_001010932.2:c.572T>C	NP_001010932.1:p.Val191Ala
XM_011516115.2:c.572T>C	XP_011514417.1:p.Val191Ala
XM_017012097.1:c.587T>C	XP_016867586.1:p.Val196Ala
XM_017012098.1:c.572T>C	XP_016867587.1:p.Val191Ala
NM_000601.6:c.587T>C MANE Select	NP_000592.3:p.Val196Ala
NM_001010931.3:c.587T>C	NP_001010931.1:p.Val196Ala
NM_001010932.3:c.572T>C	NP_001010932.1:p.Val191Ala
NM_001010933.3:c.572T>C	NP_001010933.1:p.Val191Ala
NM_001010934.3:c.587T>C	NP_001010934.1:p.Val196Ala