Canonical Allele Identifier: CA414592880

Gene: ZDHHC9

Linked Data

• dbSNP Id: rs1928084757
• MyVariant Identifiers: chrX:g.128963047T>C (hg19) ; chrX:g.129829071T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129829071T>C , CM000685.2:g.129829071T>C	GRCh38
NC_000023.10:g.128963047T>C , CM000685.1:g.128963047T>C	GRCh37
NC_000023.9:g.128790728T>C	NCBI36
NG_021387.1:g.19864A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357166.11:c.238A>G MANE Select	ENSP00000349689.6:p.Met80Val
ENST00000357166.10:c.238A>G	ENSP00000349689.6:p.Met80Val
ENST00000371064.7:c.238A>G	ENSP00000360103.3:p.Met80Val
ENST00000406492.2:c.238A>G	ENSP00000383991.2:p.Met80Val
ENST00000433917.5:c.117A>G
NM_001008222.2:c.238A>G	NP_001008223.1:p.Met80Val
NM_016032.3:c.238A>G	NP_057116.2:p.Met80Val
XM_011531347.1:c.238A>G	XP_011529649.1:p.Met80Val
XM_011531348.1:c.238A>G	XP_011529650.1:p.Met80Val
XM_011531348.3:c.238A>G	XP_011529650.1:p.Met80Val
XR_001755694.2:n.632A>G
NM_016032.4:c.238A>G MANE Select	NP_057116.2:p.Met80Val
NM_001008222.3:c.238A>G	NP_001008223.1:p.Met80Val