Canonical Allele Identifier: CA414592737

Gene: ZDHHC9

Linked Data

• MyVariant Identifiers: chrX:g.128963028G>T (hg19) ; chrX:g.129829052G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129829052G>T , CM000685.2:g.129829052G>T	GRCh38
NC_000023.10:g.128963028G>T , CM000685.1:g.128963028G>T	GRCh37
NC_000023.9:g.128790709G>T	NCBI36
NG_021387.1:g.19883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.257C>A MANE Select	ENSP00000349689.6:p.Thr86Asn
ENST00000357166.10:c.257C>A	ENSP00000349689.6:p.Thr86Asn
ENST00000371064.7:c.257C>A	ENSP00000360103.3:p.Thr86Asn
ENST00000406492.2:c.257C>A	ENSP00000383991.2:p.Thr86Asn
ENST00000433917.5:c.136C>A
NM_001008222.2:c.257C>A	NP_001008223.1:p.Thr86Asn
NM_016032.3:c.257C>A	NP_057116.2:p.Thr86Asn
XM_011531347.1:c.257C>A	XP_011529649.1:p.Thr86Asn
XM_011531348.1:c.257C>A	XP_011529650.1:p.Thr86Asn
XM_011531348.3:c.257C>A	XP_011529650.1:p.Thr86Asn
XR_001755694.2:n.651C>A
NM_016032.4:c.257C>A MANE Select	NP_057116.2:p.Thr86Asn
NM_001008222.3:c.257C>A	NP_001008223.1:p.Thr86Asn