Canonical Allele Identifier: CA414590367

Gene: ZDHHC9

Linked Data

• COSMIC: COSM286665
• MyVariant Identifiers: chrX:g.128957707C>A (hg19) ; chrX:g.129823731C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823731C>A , CM000685.2:g.129823731C>A	GRCh38
NC_000023.10:g.128957707C>A , CM000685.1:g.128957707C>A	GRCh37
NC_000023.9:g.128785388C>A	NCBI36
NG_021387.1:g.25204G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.435G>T MANE Select	ENSP00000349689.6:p.Lys145Asn
ENST00000357166.10:c.435G>T	ENSP00000349689.6:p.Lys145Asn
ENST00000371064.7:c.435G>T	ENSP00000360103.3:p.Lys145Asn
ENST00000406492.2:c.435G>T	ENSP00000383991.2:p.Lys145Asn
ENST00000433917.5:c.314G>T
ENST00000491039.1:n.58G>T
NM_001008222.2:c.435G>T	NP_001008223.1:p.Lys145Asn
NM_016032.3:c.435G>T	NP_057116.2:p.Lys145Asn
XM_011531347.1:c.435G>T	XP_011529649.1:p.Lys145Asn
XM_011531348.1:c.435G>T	XP_011529650.1:p.Lys145Asn
XM_011531348.3:c.435G>T	XP_011529650.1:p.Lys145Asn
XR_001755694.2:n.829G>T
NM_016032.4:c.435G>T MANE Select	NP_057116.2:p.Lys145Asn
NM_001008222.3:c.435G>T	NP_001008223.1:p.Lys145Asn