Canonical Allele Identifier: CA121152
Gene: ZDHHC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10710
ClinVar RCV Id: RCV000011456
dbSNP Id: rs606231183
MyVariant Identifiers: chrX:g.128975750C>G (hg19) chrX:g.129841774C>G (hg38)
PubMed: PMID:17436253
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129841774C>G , CM000685.2:g.129841774C>G GRCh38
NC_000023.10:g.128975750C>G , CM000685.1:g.128975750C>G GRCh37
NC_000023.9:g.128803431C>G NCBI36
NG_021387.1:g.7161G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357166.11:c.167+5G>C MANE Select ENSP00000349689.6:n.167+5G>C
ENST00000357166.10:c.167+5G>C ENSP00000349689.6:n.167+5G>C
ENST00000371064.7:c.167+5G>C ENSP00000360103.3:n.167+5G>C
ENST00000406492.2:c.167+5G>C ENSP00000383991.2:n.167+5G>C
ENST00000433917.5:c.46+5G>C
NM_001008222.2:c.167+5G>C NP_001008223.1:n.167+5G>C
NM_016032.3:c.167+5G>C NP_057116.2:n.167+5G>C
XM_011531347.1:c.167+5G>C XP_011529649.1:n.167+5G>C
XM_011531348.1:c.167+5G>C XP_011529650.1:n.167+5G>C
XM_011531348.3:c.167+5G>C XP_011529650.1:n.167+5G>C
XR_001755694.2:n.561+5G>C
NM_016032.4:c.167+5G>C MANE Select NP_057116.2:n.167+5G>C
NM_001008222.3:c.167+5G>C NP_001008223.1:n.167+5G>C
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