Canonical Allele Identifier: CA1720888245
Gene: HGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81729635T= , CM000669.2:g.81729635T= GRCh38
NC_000007.13:g.81358951T= , CM000669.1:g.81358951T= GRCh37
NC_000007.12:g.81196887T= NCBI36
NG_016274.1:g.45502A=
NG_016274.2:g.45502A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.1010A= MANE Select ENSP00000222390.5:p.His337=
ENST00000457544.7:c.995A= ENSP00000391238.2:p.His332=
ENST00000222390.9:c.1010A= ENSP00000222390.5:p.His337=
ENST00000457544.6:c.995A= ENSP00000391238.2:p.His332=
NM_000601.4:c.1010A= NP_000592.3:p.His337=
NM_001010932.1:c.995A= NP_001010932.1:p.His332=
XM_006715956.2:c.1010A= XP_006716019.1:p.His337=
XM_011516115.1:c.995A= XP_011514417.1:p.His332=
NM_000601.5:c.1010A= NP_000592.3:p.His337=
NM_001010932.2:c.995A= NP_001010932.1:p.His332=
XM_011516115.2:c.995A= XP_011514417.1:p.His332=
NM_000601.6:c.1010A= MANE Select NP_000592.3:p.His337=
NM_001010932.3:c.995A= NP_001010932.1:p.His332=