Canonical Allele Identifier: CA2458188298
Gene: ZDHHC9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129823636A= , CM000685.2:g.129823636A= GRCh38
NC_000023.10:g.128957612A= , CM000685.1:g.128957612A= GRCh37
NC_000023.9:g.128785293A= NCBI36
NG_021387.1:g.25299T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357166.11:c.487+43T= MANE Select ENSP00000349689.6:n.487+43T=
ENST00000357166.10:c.487+43T= ENSP00000349689.6:n.487+43T=
ENST00000371064.7:c.487+43T= ENSP00000360103.3:n.487+43T=
ENST00000406492.2:c.487+43T= ENSP00000383991.2:n.487+43T=
ENST00000433917.5:c.366+43T=
ENST00000491039.1:n.110+43T=
NM_001008222.2:c.487+43T= NP_001008223.1:n.487+43T=
NM_016032.3:c.487+43T= NP_057116.2:n.487+43T=
XM_011531347.1:c.487+43T= XP_011529649.1:n.487+43T=
XM_011531348.1:c.487+43T= XP_011529650.1:n.487+43T=
XM_011531348.3:c.487+43T= XP_011529650.1:n.487+43T=
XR_001755694.2:n.881+43T=
NM_016032.4:c.487+43T= MANE Select NP_057116.2:n.487+43T=
NM_001008222.3:c.487+43T= NP_001008223.1:n.487+43T=