Canonical Allele Identifier: CA456129446

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81381479T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81752163T>A , CM000669.2:g.81752163T>A	GRCh38
NC_000007.13:g.81381479T>A , CM000669.1:g.81381479T>A	GRCh37
NC_000007.12:g.81219415T>A	NCBI36
NG_016274.1:g.22974A>T
NG_016274.2:g.22974A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.582A>T MANE Select	ENSP00000222390.5:p.Pro194=
ENST00000423064.7:c.582A>T	ENSP00000413829.2:p.Pro194=
ENST00000444829.7:c.582A>T	ENSP00000389854.2:p.Pro194=
ENST00000453411.6:c.567A>T	ENSP00000408270.1:p.Pro189=
ENST00000457544.7:c.567A>T	ENSP00000391238.2:p.Pro189=
ENST00000465234.2:c.567A>T	ENSP00000494355.1:p.Pro189=
ENST00000222390.9:c.582A>T	ENSP00000222390.5:p.Pro194=
ENST00000423064.6:c.582A>T	ENSP00000413829.2:p.Pro194=
ENST00000444829.6:c.582A>T	ENSP00000389854.2:p.Pro194=
ENST00000453411.5:c.567A>T	ENSP00000408270.1:p.Pro189=
ENST00000457544.6:c.567A>T	ENSP00000391238.2:p.Pro189=
ENST00000465234.1:n.595A>T
NM_000601.4:c.582A>T	NP_000592.3:p.Pro194=
NM_001010931.1:c.582A>T	NP_001010931.1:p.Pro194=
NM_001010931.2:c.582A>T	NP_001010931.1:p.Pro194=
NM_001010932.1:c.567A>T	NP_001010932.1:p.Pro189=
NM_001010933.1:c.567A>T	NP_001010933.1:p.Pro189=
NM_001010933.2:c.567A>T	NP_001010933.1:p.Pro189=
NM_001010934.1:c.582A>T	NP_001010934.1:p.Pro194=
NM_001010934.2:c.582A>T	NP_001010934.1:p.Pro194=
XM_006715956.2:c.582A>T	XP_006716019.1:p.Pro194=
XM_011516115.1:c.567A>T	XP_011514417.1:p.Pro189=
NM_000601.5:c.582A>T	NP_000592.3:p.Pro194=
NM_001010932.2:c.567A>T	NP_001010932.1:p.Pro189=
XM_011516115.2:c.567A>T	XP_011514417.1:p.Pro189=
XM_017012097.1:c.582A>T	XP_016867586.1:p.Pro194=
XM_017012098.1:c.567A>T	XP_016867587.1:p.Pro189=
NM_000601.6:c.582A>T MANE Select	NP_000592.3:p.Pro194=
NM_001010931.3:c.582A>T	NP_001010931.1:p.Pro194=
NM_001010932.3:c.567A>T	NP_001010932.1:p.Pro189=
NM_001010933.3:c.567A>T	NP_001010933.1:p.Pro189=
NM_001010934.3:c.582A>T	NP_001010934.1:p.Pro194=