Canonical Allele Identifier: CA414592349

Gene: ZDHHC9

Linked Data

• MyVariant Identifiers: chrX:g.128962960T>A (hg19) ; chrX:g.129828984T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129828984T>A , CM000685.2:g.129828984T>A	GRCh38
NC_000023.10:g.128962960T>A , CM000685.1:g.128962960T>A	GRCh37
NC_000023.9:g.128790641T>A	NCBI36
NG_021387.1:g.19951A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000357166.11:c.325A>T MANE Select	ENSP00000349689.6:p.Ile109Leu
ENST00000357166.10:c.325A>T	ENSP00000349689.6:p.Ile109Leu
ENST00000371064.7:c.325A>T	ENSP00000360103.3:p.Ile109Leu
ENST00000406492.2:c.325A>T	ENSP00000383991.2:p.Ile109Leu
ENST00000433917.5:c.204A>T
NM_001008222.2:c.325A>T	NP_001008223.1:p.Ile109Leu
NM_016032.3:c.325A>T	NP_057116.2:p.Ile109Leu
XM_011531347.1:c.325A>T	XP_011529649.1:p.Ile109Leu
XM_011531348.1:c.325A>T	XP_011529650.1:p.Ile109Leu
XM_011531348.3:c.325A>T	XP_011529650.1:p.Ile109Leu
XR_001755694.2:n.719A>T
NM_016032.4:c.325A>T MANE Select	NP_057116.2:p.Ile109Leu
NM_001008222.3:c.325A>T	NP_001008223.1:p.Ile109Leu