Canonical Allele Identifier: CA10450106
Gene: HDAC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72351778G>A , CM000685.2:g.72351778G>A GRCh38
NC_000023.10:g.71571628G>A , CM000685.1:g.71571628G>A GRCh37
NC_000023.9:g.71488353G>A NCBI36
NG_015851.1:g.226326C>T

Transcript Alleles

HGVS Amino-acid Change
NM_018486.3:c.1066C>T MANE Select NP_060956.1:p.Arg356Cys
ENST00000373573.9:c.1066C>T MANE Select ENSP00000362674.3:p.Arg356Cys
NM_001166418.1:c.793C>T NP_001159890.1:p.Arg265Cys
NM_001166418.2:c.793C>T NP_001159890.1:p.Arg265Cys
NM_018486.2:c.1066C>T NP_060956.1:p.Arg356Cys
NR_051952.1:n.1266C>T
NR_051952.2:n.1006C>T
ENST00000373568.7:c.1066C>T ENSP00000362669.3:p.Arg356Cys
ENST00000373573.7:c.1066C>T ENSP00000362674.3:p.Arg356Cys
ENST00000373583.5:c.165-22069C>T ENSP00000362685.1:n.165-22069C>T
ENST00000373583.6:c.988C>T ENSP00000362685.2:p.Arg330Cys
ENST00000373589.8:c.793C>T ENSP00000362691.4:p.Arg265Cys
ENST00000373589.9:c.793C>T ENSP00000362691.4:p.Arg265Cys
ENST00000470998.1:n.239C>T
ENST00000470998.2:c.243C>T
ENST00000647594.1:c.1066C>T ENSP00000496814.1:p.Arg356Cys
ENST00000647613.1:c.*819C>T ENSP00000497911.1:n.*819C>T
ENST00000647641.1:n.1153C>T
ENST00000647654.1:c.793C>T ENSP00000497568.1:p.Arg265Cys
ENST00000647859.1:c.1066C>T ENSP00000497530.1:p.Arg356Cys
ENST00000647886.1:c.1066C>T ENSP00000497188.1:p.Arg356Cys
ENST00000647980.1:c.1060C>T ENSP00000498002.1:p.Arg354Cys
ENST00000648139.1:c.766C>T ENSP00000496818.1:p.Arg256Cys
ENST00000648276.1:c.450C>T ENSP00000497619.1:p.Thr150=
ENST00000648452.1:c.1066C>T ENSP00000497268.1:p.Arg356Cys
ENST00000648459.1:c.463C>T ENSP00000498072.1:p.Arg155Cys
ENST00000648504.1:c.1007C>T ENSP00000497668.1:n.1007C>T
ENST00000648711.1:c.695C>T ENSP00000498040.1:n.695C>T
ENST00000648731.1:c.1172C>T
ENST00000648834.1:c.*146C>T ENSP00000497764.1:n.*146C>T
ENST00000648850.1:c.705C>T
ENST00000648855.1:n.990C>T
ENST00000648922.1:c.1066C>T ENSP00000497072.1:p.Arg356Cys
ENST00000648939.1:c.*146C>T ENSP00000497442.1:n.*146C>T
ENST00000649097.1:c.1066C>T ENSP00000497551.1:p.Arg356Cys
ENST00000649181.1:c.*428C>T ENSP00000498150.1:n.*428C>T
ENST00000649274.1:c.1004C>T ENSP00000497032.1:n.1004C>T
ENST00000649543.1:c.*670C>T ENSP00000496826.1:n.*670C>T
ENST00000650076.1:c.423C>T
ENST00000650471.1:c.*510C>T ENSP00000498027.1:n.*510C>T
ENST00000650604.1:c.493C>T ENSP00000497105.1:p.Arg165Cys
XM_011530986.1:c.1066C>T XP_011529288.1:p.Arg356Cys
XM_011530986.3:c.1066C>T XP_011529288.3:p.Arg356Cys
XM_017029640.2:c.988C>T XP_016885129.2:p.Arg330Cys
XM_017029641.2:c.988C>T XP_016885130.2:p.Arg330Cys
XM_017029642.1:c.907C>T XP_016885131.1:p.Arg303Cys
XM_017029643.2:c.880C>T XP_016885132.1:p.Arg294Cys
XM_017029644.2:c.829C>T XP_016885133.1:p.Arg277Cys
XM_017029645.2:c.880C>T XP_016885134.1:p.Arg294Cys
XM_017029646.1:c.679C>T XP_016885135.1:p.Arg227Cys
XM_024452405.1:c.481C>T XP_024308173.1:p.Arg161Cys
XR_001755711.2:n.1152C>T
XR_002958779.1:n.1248C>T
XR_002958780.1:n.1156C>T
XR_002958781.1:n.1156C>T
XR_002958783.1:n.1132C>T
XR_938402.1:n.1152C>T
XR_938402.3:n.1152C>T