Canonical Allele Identifier: CA2579699492

Gene: ZDHHC9

Linked Data

• gnomAD v4: X-129823634-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823634C>A , CM000685.2:g.129823634C>A	GRCh38
NC_000023.10:g.128957610C>A , CM000685.1:g.128957610C>A	GRCh37
NC_000023.9:g.128785291C>A	NCBI36
NG_021387.1:g.25301G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.487+45G>T MANE Select	ENSP00000349689.6:n.487+45G>T
ENST00000357166.10:c.487+45G>T	ENSP00000349689.6:n.487+45G>T
ENST00000371064.7:c.487+45G>T	ENSP00000360103.3:n.487+45G>T
ENST00000406492.2:c.487+45G>T	ENSP00000383991.2:n.487+45G>T
ENST00000433917.5:c.366+45G>T
ENST00000491039.1:n.110+45G>T
NM_001008222.2:c.487+45G>T	NP_001008223.1:n.487+45G>T
NM_016032.3:c.487+45G>T	NP_057116.2:n.487+45G>T
XM_011531347.1:c.487+45G>T	XP_011529649.1:n.487+45G>T
XM_011531348.1:c.487+45G>T	XP_011529650.1:n.487+45G>T
XM_011531348.3:c.487+45G>T	XP_011529650.1:n.487+45G>T
XR_001755694.2:n.881+45G>T
NM_016032.4:c.487+45G>T MANE Select	NP_057116.2:n.487+45G>T
NM_001008222.3:c.487+45G>T	NP_001008223.1:n.487+45G>T