Canonical Allele Identifier: CA2694670787

Gene: ZDHHC9

Linked Data

• gnomAD v4: X-129823660-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823663dup , CM000685.2:g.129823663dup	GRCh38
NC_000023.10:g.128957639dup , CM000685.1:g.128957639dup	GRCh37
NC_000023.9:g.128785320dup	NCBI36
NG_021387.1:g.25274dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.487+18dup MANE Select	ENSP00000349689.6:n.487+18dup
ENST00000357166.10:c.487+18dup	ENSP00000349689.6:n.487+18dup
ENST00000371064.7:c.487+18dup	ENSP00000360103.3:n.487+18dup
ENST00000406492.2:c.487+18dup	ENSP00000383991.2:n.487+18dup
ENST00000433917.5:c.366+18dup
ENST00000491039.1:n.110+18dup
NM_001008222.2:c.487+18dup	NP_001008223.1:n.487+18dup
NM_016032.3:c.487+18dup	NP_057116.2:n.487+18dup
XM_011531347.1:c.487+18dup	XP_011529649.1:n.487+18dup
XM_011531348.1:c.487+18dup	XP_011529650.1:n.487+18dup
XM_011531348.3:c.487+18dup	XP_011529650.1:n.487+18dup
XR_001755694.2:n.881+18dup
NM_016032.4:c.487+18dup MANE Select	NP_057116.2:n.487+18dup
NM_001008222.3:c.487+18dup	NP_001008223.1:n.487+18dup