Canonical Allele Identifier: CA2573159206

Gene: ZDHHC9

Linked Data

• ClinVar Variation Id: 1558589
• ClinVar RCV Id: RCV002200033
• dbSNP Id: rs2124124472

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129828965del , CM000685.2:g.129828965del	GRCh38
NC_000023.10:g.128962941del , CM000685.1:g.128962941del	GRCh37
NC_000023.9:g.128790622del	NCBI36
NG_021387.1:g.19970del

Transcript Alleles

HGVS	Amino-acid change
ENST00000357166.11:c.328+16del MANE Select	ENSP00000349689.6:n.328+16del
ENST00000357166.10:c.328+16del	ENSP00000349689.6:n.328+16del
ENST00000371064.7:c.328+16del	ENSP00000360103.3:n.328+16del
ENST00000406492.2:c.328+16del	ENSP00000383991.2:n.328+16del
ENST00000433917.5:c.207+16del
NM_001008222.2:c.328+16del	NP_001008223.1:n.328+16del
NM_016032.3:c.328+16del	NP_057116.2:n.328+16del
XM_011531347.1:c.328+16del	XP_011529649.1:n.328+16del
XM_011531348.1:c.328+16del	XP_011529650.1:n.328+16del
XM_011531348.3:c.328+16del	XP_011529650.1:n.328+16del
XR_001755694.2:n.722+16del
NM_016032.4:c.328+16del MANE Select	NP_057116.2:n.328+16del
NM_001008222.3:c.328+16del	NP_001008223.1:n.328+16del