Canonical Allele Identifier: CA121153
Gene: ZDHHC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10711
ClinVar RCV Id: RCV000011457 RCV001091717 RCV001260822
dbSNP Id: rs137852214
COSMIC: COSM4137670 COSM4137671
MyVariant Identifiers: chrX:g.128957700G>A (hg19) chrX:g.129823724G>A (hg38)
PubMed: PMID:17436253 PMID:28135719
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129823724G>A , CM000685.2:g.129823724G>A GRCh38
NC_000023.10:g.128957700G>A , CM000685.1:g.128957700G>A GRCh37
NC_000023.9:g.128785381G>A NCBI36
NG_021387.1:g.25211C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000357166.11:c.442C>T MANE Select ENSP00000349689.6:p.Arg148Trp
ENST00000357166.10:c.442C>T ENSP00000349689.6:p.Arg148Trp
ENST00000371064.7:c.442C>T ENSP00000360103.3:p.Arg148Trp
ENST00000406492.2:c.442C>T ENSP00000383991.2:p.Arg148Trp
ENST00000433917.5:c.321C>T
ENST00000491039.1:n.65C>T
NM_001008222.2:c.442C>T NP_001008223.1:p.Arg148Trp
NM_016032.3:c.442C>T NP_057116.2:p.Arg148Trp
XM_011531347.1:c.442C>T XP_011529649.1:p.Arg148Trp
XM_011531348.1:c.442C>T XP_011529650.1:p.Arg148Trp
XM_011531348.3:c.442C>T XP_011529650.1:p.Arg148Trp
XR_001755694.2:n.836C>T
NM_016032.4:c.442C>T MANE Select NP_057116.2:p.Arg148Trp
NM_001008222.3:c.442C>T NP_001008223.1:p.Arg148Trp
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