Canonical Allele Identifier: CA335100810

Gene: ZDHHC9

Linked Data

• ClinVar Variation Id: 1582568
• ClinVar RCV Id: RCV002111227
• dbSNP Id: rs769825368
• gnomAD v4: X-129828970-G-A
• MyVariant Identifiers: chrX:g.128962946G>A (hg19) ; chrX:g.129828970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129828970G>A , CM000685.2:g.129828970G>A	GRCh38
NC_000023.10:g.128962946G>A , CM000685.1:g.128962946G>A	GRCh37
NC_000023.9:g.128790627G>A	NCBI36
NG_021387.1:g.19965C>T

Transcript Alleles

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