Canonical Allele Identifier: CA121151
Gene: ZDHHC9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129829134_129829137del , CM000685.2:g.129829134_129829137del GRCh38
NC_000023.10:g.128963110_128963113del , CM000685.1:g.128963110_128963113del GRCh37
NC_000023.9:g.128790791_128790794del NCBI36
NG_021387.1:g.19798_19801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357166.11:c.172_175del MANE Select ENSP00000349689.6:p.Arg58ThrfsTer26
ENST00000357166.10:c.172_175del ENSP00000349689.6:p.Arg58ThrfsTer26
ENST00000371064.7:c.172_175del ENSP00000360103.3:p.Arg58ThrfsTer26
ENST00000406492.2:c.172_175del ENSP00000383991.2:p.Arg58ThrfsTer26
ENST00000433917.5:c.51_54del
NM_001008222.2:c.172_175del NP_001008223.1:p.Arg58ThrfsTer26
NM_016032.3:c.172_175del NP_057116.2:p.Arg58ThrfsTer26
XM_011531347.1:c.172_175del XP_011529649.1:p.Arg58ThrfsTer26
XM_011531348.1:c.172_175del XP_011529650.1:p.Arg58ThrfsTer26
XM_011531348.3:c.172_175del XP_011529650.1:p.Arg58ThrfsTer26
XR_001755694.2:n.566_569del
NM_016032.4:c.172_175del MANE Select NP_057116.2:p.Arg58ThrfsTer26
NM_001008222.3:c.172_175del NP_001008223.1:p.Arg58ThrfsTer26
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