Canonical Allele Identifier: CA2458189904
Gene: ZDHHC9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129828970G= , CM000685.2:g.129828970G= GRCh38
NC_000023.10:g.128962946G= , CM000685.1:g.128962946G= GRCh37
NC_000023.9:g.128790627G= NCBI36
NG_021387.1:g.19965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000357166.11:c.328+11C= MANE Select ENSP00000349689.6:n.328+11C=
ENST00000357166.10:c.328+11C= ENSP00000349689.6:n.328+11C=
ENST00000371064.7:c.328+11C= ENSP00000360103.3:n.328+11C=
ENST00000406492.2:c.328+11C= ENSP00000383991.2:n.328+11C=
ENST00000433917.5:c.207+11C=
NM_001008222.2:c.328+11C= NP_001008223.1:n.328+11C=
NM_016032.3:c.328+11C= NP_057116.2:n.328+11C=
XM_011531347.1:c.328+11C= XP_011529649.1:n.328+11C=
XM_011531348.1:c.328+11C= XP_011529650.1:n.328+11C=
XM_011531348.3:c.328+11C= XP_011529650.1:n.328+11C=
XR_001755694.2:n.722+11C=
NM_016032.4:c.328+11C= MANE Select NP_057116.2:n.328+11C=
NM_001008222.3:c.328+11C= NP_001008223.1:n.328+11C=