Canonical Allele Identifier: CA2843305714

Gene: ZDHHC9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129823638_129823639del , CM000685.2:g.129823638_129823639del	GRCh38
NC_000023.10:g.128957614_128957615del , CM000685.1:g.128957614_128957615del	GRCh37
NC_000023.9:g.128785295_128785296del	NCBI36
NG_021387.1:g.25297_25298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357166.11:c.487+41_487+42del MANE Select	ENSP00000349689.6:n.487+41_487+42del
ENST00000357166.10:c.487+41_487+42del	ENSP00000349689.6:n.487+41_487+42del
ENST00000371064.7:c.487+41_487+42del	ENSP00000360103.3:n.487+41_487+42del
ENST00000406492.2:c.487+41_487+42del	ENSP00000383991.2:n.487+41_487+42del
ENST00000433917.5:c.366+41_366+42del
ENST00000491039.1:n.110+41_110+42del
NM_001008222.2:c.487+41_487+42del	NP_001008223.1:n.487+41_487+42del
NM_016032.3:c.487+41_487+42del	NP_057116.2:n.487+41_487+42del
XM_011531347.1:c.487+41_487+42del	XP_011529649.1:n.487+41_487+42del
XM_011531348.1:c.487+41_487+42del	XP_011529650.1:n.487+41_487+42del
XM_011531348.3:c.487+41_487+42del	XP_011529650.1:n.487+41_487+42del
XR_001755694.2:n.881+41_881+42del
NM_016032.4:c.487+41_487+42del MANE Select	NP_057116.2:n.487+41_487+42del
NM_001008222.3:c.487+41_487+42del	NP_001008223.1:n.487+41_487+42del