Canonical Allele Identifier: CA367870783
Gene: HGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81729636G>C , CM000669.2:g.81729636G>C GRCh38
NC_000007.13:g.81358952G>C , CM000669.1:g.81358952G>C GRCh37
NC_000007.12:g.81196888G>C NCBI36
NG_016274.1:g.45501C>G
NG_016274.2:g.45501C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222390.11:c.1009C>G MANE Select ENSP00000222390.5:p.His337Asp
ENST00000457544.7:c.994C>G ENSP00000391238.2:p.His332Asp
ENST00000222390.9:c.1009C>G ENSP00000222390.5:p.His337Asp
ENST00000457544.6:c.994C>G ENSP00000391238.2:p.His332Asp
NM_000601.4:c.1009C>G NP_000592.3:p.His337Asp
NM_001010932.1:c.994C>G NP_001010932.1:p.His332Asp
XM_006715956.2:c.1009C>G XP_006716019.1:p.His337Asp
XM_011516115.1:c.994C>G XP_011514417.1:p.His332Asp
NM_000601.5:c.1009C>G NP_000592.3:p.His337Asp
NM_001010932.2:c.994C>G NP_001010932.1:p.His332Asp
XM_011516115.2:c.994C>G XP_011514417.1:p.His332Asp
NM_000601.6:c.1009C>G MANE Select NP_000592.3:p.His337Asp
NM_001010932.3:c.994C>G NP_001010932.1:p.His332Asp