Canonical Allele Identifier: CA10513547

Gene: ZDHHC9

Linked Data

• ClinVar Variation Id: 1113977
• ClinVar RCV Id: RCV001441523
• dbSNP Id: rs377127210
• ExAC: X:128957713 T / C
• gnomAD v2: X-128957713-T-C
• gnomAD v4: X-129823737-T-C
• MyVariant Identifiers: chrX:g.128957713T>C (hg19) ; chrX:g.129823737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823737T>C , CM000685.2:g.129823737T>C	GRCh38
NC_000023.10:g.128957713T>C , CM000685.1:g.128957713T>C	GRCh37
NC_000023.9:g.128785394T>C	NCBI36
NG_021387.1:g.25198A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357166.11:c.429A>G MANE Select	ENSP00000349689.6:p.Thr143=
ENST00000357166.10:c.429A>G	ENSP00000349689.6:p.Thr143=
ENST00000371064.7:c.429A>G	ENSP00000360103.3:p.Thr143=
ENST00000406492.2:c.429A>G	ENSP00000383991.2:p.Thr143=
ENST00000433917.5:c.308A>G
ENST00000491039.1:n.52A>G
NM_001008222.2:c.429A>G	NP_001008223.1:p.Thr143=
NM_016032.3:c.429A>G	NP_057116.2:p.Thr143=
XM_011531347.1:c.429A>G	XP_011529649.1:p.Thr143=
XM_011531348.1:c.429A>G	XP_011529650.1:p.Thr143=
XM_011531348.3:c.429A>G	XP_011529650.1:p.Thr143=
XR_001755694.2:n.823A>G
NM_016032.4:c.429A>G MANE Select	NP_057116.2:p.Thr143=
NM_001008222.3:c.429A>G	NP_001008223.1:p.Thr143=