Canonical Allele Identifier: CA16621197
Gene: ZDHHC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 418668
ClinVar RCV Id: RCV000484510
dbSNP Id: rs1064793355
MyVariant Identifiers: chrX:g.128963034A>G (hg19) chrX:g.129829058A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129829058A>G , CM000685.2:g.129829058A>G GRCh38
NC_000023.10:g.128963034A>G , CM000685.1:g.128963034A>G GRCh37
NC_000023.9:g.128790715A>G NCBI36
NG_021387.1:g.19877T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357166.11:c.251T>C MANE Select ENSP00000349689.6:p.Leu84Ser
ENST00000357166.10:c.251T>C ENSP00000349689.6:p.Leu84Ser
ENST00000371064.7:c.251T>C ENSP00000360103.3:p.Leu84Ser
ENST00000406492.2:c.251T>C ENSP00000383991.2:p.Leu84Ser
ENST00000433917.5:c.130T>C
NM_001008222.2:c.251T>C NP_001008223.1:p.Leu84Ser
NM_016032.3:c.251T>C NP_057116.2:p.Leu84Ser
XM_011531347.1:c.251T>C XP_011529649.1:p.Leu84Ser
XM_011531348.1:c.251T>C XP_011529650.1:p.Leu84Ser
XM_011531348.3:c.251T>C XP_011529650.1:p.Leu84Ser
XR_001755694.2:n.645T>C
NM_016032.4:c.251T>C MANE Select NP_057116.2:p.Leu84Ser
NM_001008222.3:c.251T>C NP_001008223.1:p.Leu84Ser
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