Canonical Allele Identifier: CA414592329

Gene: ZDHHC9

Linked Data

• ClinVar Variation Id: 504233
• ClinVar RCV Id: RCV000598660
• dbSNP Id: rs1556007364
• MyVariant Identifiers: chrX:g.128962956C>T (hg19) ; chrX:g.129828980C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129828980C>T , CM000685.2:g.129828980C>T	GRCh38
NC_000023.10:g.128962956C>T , CM000685.1:g.128962956C>T	GRCh37
NC_000023.9:g.128790637C>T	NCBI36
NG_021387.1:g.19955G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357166.11:c.328+1G>A MANE Select	ENSP00000349689.6:n.328+1G>A
ENST00000357166.10:c.328+1G>A	ENSP00000349689.6:n.328+1G>A
ENST00000371064.7:c.328+1G>A	ENSP00000360103.3:n.328+1G>A
ENST00000406492.2:c.328+1G>A	ENSP00000383991.2:n.328+1G>A
ENST00000433917.5:c.207+1G>A
NM_001008222.2:c.328+1G>A	NP_001008223.1:n.328+1G>A
NM_016032.3:c.328+1G>A	NP_057116.2:n.328+1G>A
XM_011531347.1:c.328+1G>A	XP_011529649.1:n.328+1G>A
XM_011531348.1:c.328+1G>A	XP_011529650.1:n.328+1G>A
XM_011531348.3:c.328+1G>A	XP_011529650.1:n.328+1G>A
XR_001755694.2:n.722+1G>A
NM_016032.4:c.328+1G>A MANE Select	NP_057116.2:n.328+1G>A
NM_001008222.3:c.328+1G>A	NP_001008223.1:n.328+1G>A