Canonical Allele Identifier: CA10513558

Gene: ZDHHC9

Linked Data

• ClinVar Variation Id: 1447870
• ClinVar RCV Id: RCV001996957 ; RCV003407999
• dbSNP Id: rs763845850
• ExAC: X:128957814 C / CT
• gnomAD v2: X-128957814-C-CT
• gnomAD v4: X-129823838-C-CT
• MyVariant Identifiers: chrX:g.128957814_128957815insT (hg19) ; chrX:g.129823838_129823839insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823839dup , CM000685.2:g.129823839dup	GRCh38
NC_000023.10:g.128957815dup , CM000685.1:g.128957815dup	GRCh37
NC_000023.9:g.128785496dup	NCBI36
NG_021387.1:g.25096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.329-2dup MANE Select	ENSP00000349689.6:n.329-2dup
ENST00000357166.10:c.329-2dup	ENSP00000349689.6:n.329-2dup
ENST00000371064.7:c.329-2dup	ENSP00000360103.3:n.329-2dup
ENST00000406492.2:c.329-2dup	ENSP00000383991.2:n.329-2dup
ENST00000433917.5:c.208-2dup
NM_001008222.2:c.329-2dup	NP_001008223.1:n.329-2dup
NM_016032.3:c.329-2dup	NP_057116.2:n.329-2dup
XM_011531347.1:c.329-2dup	XP_011529649.1:n.329-2dup
XM_011531348.1:c.329-2dup	XP_011529650.1:n.329-2dup
XM_011531348.3:c.329-2dup	XP_011529650.1:n.329-2dup
XR_001755694.2:n.723-2dup
NM_016032.4:c.329-2dup MANE Select	NP_057116.2:n.329-2dup
NM_001008222.3:c.329-2dup	NP_001008223.1:n.329-2dup