Canonical Allele Identifier: CA335099301

Gene: ZDHHC9

Linked Data

• dbSNP Id: rs760562871
• gnomAD v3: X-129823917-TG-T
• gnomAD v4: X-129823917-TG-T
• MyVariant Identifiers: chrX:g.128957894del (hg19) ; chrX:g.129823918del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823922del , CM000685.2:g.129823922del	GRCh38
NC_000023.10:g.128957898del , CM000685.1:g.128957898del	GRCh37
NC_000023.9:g.128785579del	NCBI36
NG_021387.1:g.25017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.329-81del MANE Select	ENSP00000349689.6:n.329-81del
ENST00000357166.10:c.329-81del	ENSP00000349689.6:n.329-81del
ENST00000371064.7:c.329-81del	ENSP00000360103.3:n.329-81del
ENST00000406492.2:c.329-81del	ENSP00000383991.2:n.329-81del
ENST00000433917.5:c.208-81del
NM_001008222.2:c.329-81del	NP_001008223.1:n.329-81del
NM_016032.3:c.329-81del	NP_057116.2:n.329-81del
XM_011531347.1:c.329-81del	XP_011529649.1:n.329-81del
XM_011531348.1:c.329-81del	XP_011529650.1:n.329-81del
XM_011531348.3:c.329-81del	XP_011529650.1:n.329-81del
XR_001755694.2:n.723-81del
NM_016032.4:c.329-81del MANE Select	NP_057116.2:n.329-81del
NM_001008222.3:c.329-81del	NP_001008223.1:n.329-81del