Canonical Allele Identifier: CA367874766
Gene: HGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.81752151G>T , CM000669.2:g.81752151G>T GRCh38
NC_000007.13:g.81381467G>T , CM000669.1:g.81381467G>T GRCh37
NC_000007.12:g.81219403G>T NCBI36
NG_016274.1:g.22986C>A
NG_016274.2:g.22986C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222390.11:c.594C>A MANE Select ENSP00000222390.5:p.Tyr198Ter
ENST00000423064.7:c.594C>A ENSP00000413829.2:p.Tyr198Ter
ENST00000444829.7:c.594C>A ENSP00000389854.2:p.Tyr198Ter
ENST00000453411.6:c.579C>A ENSP00000408270.1:p.Tyr193Ter
ENST00000457544.7:c.579C>A ENSP00000391238.2:p.Tyr193Ter
ENST00000465234.2:c.579C>A ENSP00000494355.1:p.Tyr193Ter
ENST00000222390.9:c.594C>A ENSP00000222390.5:p.Tyr198Ter
ENST00000423064.6:c.594C>A ENSP00000413829.2:p.Tyr198Ter
ENST00000444829.6:c.594C>A ENSP00000389854.2:p.Tyr198Ter
ENST00000453411.5:c.579C>A ENSP00000408270.1:p.Tyr193Ter
ENST00000457544.6:c.579C>A ENSP00000391238.2:p.Tyr193Ter
ENST00000465234.1:n.607C>A
NM_000601.4:c.594C>A NP_000592.3:p.Tyr198Ter
NM_001010931.1:c.594C>A NP_001010931.1:p.Tyr198Ter
NM_001010931.2:c.594C>A NP_001010931.1:p.Tyr198Ter
NM_001010932.1:c.579C>A NP_001010932.1:p.Tyr193Ter
NM_001010933.1:c.579C>A NP_001010933.1:p.Tyr193Ter
NM_001010933.2:c.579C>A NP_001010933.1:p.Tyr193Ter
NM_001010934.1:c.594C>A NP_001010934.1:p.Tyr198Ter
NM_001010934.2:c.594C>A NP_001010934.1:p.Tyr198Ter
XM_006715956.2:c.594C>A XP_006716019.1:p.Tyr198Ter
XM_011516115.1:c.579C>A XP_011514417.1:p.Tyr193Ter
NM_000601.5:c.594C>A NP_000592.3:p.Tyr198Ter
NM_001010932.2:c.579C>A NP_001010932.1:p.Tyr193Ter
XM_011516115.2:c.579C>A XP_011514417.1:p.Tyr193Ter
XM_017012097.1:c.594C>A XP_016867586.1:p.Tyr198Ter
XM_017012098.1:c.579C>A XP_016867587.1:p.Tyr193Ter
NM_000601.6:c.594C>A MANE Select NP_000592.3:p.Tyr198Ter
NM_001010931.3:c.594C>A NP_001010931.1:p.Tyr198Ter
NM_001010932.3:c.579C>A NP_001010932.1:p.Tyr193Ter
NM_001010933.3:c.579C>A NP_001010933.1:p.Tyr193Ter
NM_001010934.3:c.594C>A NP_001010934.1:p.Tyr198Ter