Canonical Allele Identifier: CA367876338

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81769888A>C , CM000669.2:g.81769888A>C	GRCh38
NC_000007.13:g.81399204A>C , CM000669.1:g.81399204A>C	GRCh37
NC_000007.12:g.81237140A>C	NCBI36
NG_016274.1:g.5249T>G
NG_016274.2:g.5249T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000601.6:c.84T>G MANE Select	NP_000592.3:p.Tyr28Ter
ENST00000222390.11:c.84T>G MANE Select	ENSP00000222390.5:p.Tyr28Ter
NM_000601.4:c.84T>G	NP_000592.3:p.Tyr28Ter
NM_000601.5:c.84T>G	NP_000592.3:p.Tyr28Ter
NM_001010931.1:c.84T>G	NP_001010931.1:p.Tyr28Ter
NM_001010931.2:c.84T>G	NP_001010931.1:p.Tyr28Ter
NM_001010931.3:c.84T>G	NP_001010931.1:p.Tyr28Ter
NM_001010932.1:c.84T>G	NP_001010932.1:p.Tyr28Ter
NM_001010932.2:c.84T>G	NP_001010932.1:p.Tyr28Ter
NM_001010932.3:c.84T>G	NP_001010932.1:p.Tyr28Ter
NM_001010933.1:c.84T>G	NP_001010933.1:p.Tyr28Ter
NM_001010933.2:c.84T>G	NP_001010933.1:p.Tyr28Ter
NM_001010933.3:c.84T>G	NP_001010933.1:p.Tyr28Ter
NM_001010934.1:c.84T>G	NP_001010934.1:p.Tyr28Ter
NM_001010934.2:c.84T>G	NP_001010934.1:p.Tyr28Ter
NM_001010934.3:c.84T>G	NP_001010934.1:p.Tyr28Ter
ENST00000222390.9:c.84T>G	ENSP00000222390.5:p.Tyr28Ter
ENST00000354224.10:c.84T>G	ENSP00000346164.6:p.Tyr28Ter
ENST00000412881.5:c.84T>G	ENSP00000396307.1:p.Tyr28Ter
ENST00000421558.1:c.84T>G	ENSP00000388592.1:p.Tyr28Ter
ENST00000423064.6:c.84T>G	ENSP00000413829.2:p.Tyr28Ter
ENST00000423064.7:c.84T>G	ENSP00000413829.2:p.Tyr28Ter
ENST00000444829.6:c.84T>G	ENSP00000389854.2:p.Tyr28Ter
ENST00000444829.7:c.84T>G	ENSP00000389854.2:p.Tyr28Ter
ENST00000453411.5:c.84T>G	ENSP00000408270.1:p.Tyr28Ter
ENST00000453411.6:c.84T>G	ENSP00000408270.1:p.Tyr28Ter
ENST00000457544.6:c.84T>G	ENSP00000391238.2:p.Tyr28Ter
ENST00000457544.7:c.84T>G	ENSP00000391238.2:p.Tyr28Ter
ENST00000465234.1:n.112T>G
ENST00000465234.2:c.84T>G	ENSP00000494355.1:p.Tyr28Ter
ENST00000643024.1:c.84T>G	ENSP00000496217.1:p.Tyr28Ter
XM_006715956.2:c.84T>G	XP_006716019.1:p.Tyr28Ter
XM_011516115.1:c.84T>G	XP_011514417.1:p.Tyr28Ter
XM_011516115.2:c.84T>G	XP_011514417.1:p.Tyr28Ter
XM_017012097.1:c.84T>G	XP_016867586.1:p.Tyr28Ter
XM_017012098.1:c.84T>G	XP_016867587.1:p.Tyr28Ter