Canonical Allele Identifier: CA1720888252
Gene: HGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81729647T= , CM000669.2:g.81729647T= GRCh38
NC_000007.13:g.81358963T= , CM000669.1:g.81358963T= GRCh37
NC_000007.12:g.81196899T= NCBI36
NG_016274.1:g.45490A=
NG_016274.2:g.45490A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.998A= MANE Select ENSP00000222390.5:p.Tyr333=
ENST00000457544.7:c.983A= ENSP00000391238.2:p.Tyr328=
ENST00000222390.9:c.998A= ENSP00000222390.5:p.Tyr333=
ENST00000457544.6:c.983A= ENSP00000391238.2:p.Tyr328=
NM_000601.4:c.998A= NP_000592.3:p.Tyr333=
NM_001010932.1:c.983A= NP_001010932.1:p.Tyr328=
XM_006715956.2:c.998A= XP_006716019.1:p.Tyr333=
XM_011516115.1:c.983A= XP_011514417.1:p.Tyr328=
NM_000601.5:c.998A= NP_000592.3:p.Tyr333=
NM_001010932.2:c.983A= NP_001010932.1:p.Tyr328=
XM_011516115.2:c.983A= XP_011514417.1:p.Tyr328=
NM_000601.6:c.998A= MANE Select NP_000592.3:p.Tyr333=
NM_001010932.3:c.983A= NP_001010932.1:p.Tyr328=