Canonical Allele Identifier: CA413642371
Gene: HDAC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72462084C>A , CM000685.2:g.72462084C>A GRCh38
NC_000023.10:g.71681934C>A , CM000685.1:g.71681934C>A GRCh37
NC_000023.9:g.71598659C>A NCBI36
NG_015851.1:g.116020G>T

Transcript Alleles

HGVS Amino-acid Change
NM_018486.3:c.925G>T MANE Select NP_060956.1:p.Ala309Ser
ENST00000373573.9:c.925G>T MANE Select ENSP00000362674.3:p.Ala309Ser
NM_001166418.1:c.652G>T NP_001159890.1:p.Ala218Ser
NM_001166418.2:c.652G>T NP_001159890.1:p.Ala218Ser
NM_018486.2:c.925G>T NP_060956.1:p.Ala309Ser
NR_051952.1:n.1125G>T
NR_051952.2:n.865G>T
ENST00000373568.6:c.652G>T ENSP00000362669.2:p.Ala218Ser
ENST00000373568.7:c.925G>T ENSP00000362669.3:p.Ala309Ser
ENST00000373573.7:c.925G>T ENSP00000362674.3:p.Ala309Ser
ENST00000373583.5:c.164+109973G>T ENSP00000362685.1:n.164+109973G>T
ENST00000373583.6:c.847G>T ENSP00000362685.2:p.Ala283Ser
ENST00000373589.8:c.652G>T ENSP00000362691.4:p.Ala218Ser
ENST00000373589.9:c.652G>T ENSP00000362691.4:p.Ala218Ser
ENST00000415409.5:c.847G>T ENSP00000396424.1:p.Ala283Ser
ENST00000415409.6:c.925G>T ENSP00000396424.2:p.Ala309Ser
ENST00000436675.5:c.*180G>T ENSP00000416489.1:n.*180G>T
ENST00000436675.6:c.*180G>T ENSP00000416489.1:n.*180G>T
ENST00000470998.1:n.98G>T
ENST00000470998.2:c.102G>T
ENST00000478743.2:n.1008G>T
ENST00000647594.1:c.925G>T ENSP00000496814.1:p.Ala309Ser
ENST00000647606.1:c.700G>T
ENST00000647613.1:c.*678G>T ENSP00000497911.1:n.*678G>T
ENST00000647641.1:n.1012G>T
ENST00000647654.1:c.652G>T ENSP00000497568.1:p.Ala218Ser
ENST00000647718.1:n.3440G>T
ENST00000647859.1:c.925G>T ENSP00000497530.1:p.Ala309Ser
ENST00000647886.1:c.925G>T ENSP00000497188.1:p.Ala309Ser
ENST00000647980.1:c.919G>T ENSP00000498002.1:p.Ala307Ser
ENST00000648139.1:c.625G>T ENSP00000496818.1:p.Ala209Ser
ENST00000648276.1:c.169G>T ENSP00000497619.1:p.Ala57Ser
ENST00000648298.1:c.925G>T ENSP00000496866.1:p.Ala309Ser
ENST00000648452.1:c.925G>T ENSP00000497268.1:p.Ala309Ser
ENST00000648459.1:c.322G>T ENSP00000498072.1:p.Ala108Ser
ENST00000648504.1:c.866G>T ENSP00000497668.1:n.866G>T
ENST00000648711.1:c.554G>T ENSP00000498040.1:n.554G>T
ENST00000648731.1:c.1031G>T
ENST00000648834.1:c.*5G>T ENSP00000497764.1:n.*5G>T
ENST00000648850.1:c.564G>T
ENST00000648855.1:n.849G>T
ENST00000648870.1:c.925G>T ENSP00000497599.1:p.Ala309Ser
ENST00000648922.1:c.925G>T ENSP00000497072.1:p.Ala309Ser
ENST00000648939.1:c.*5G>T ENSP00000497442.1:n.*5G>T
ENST00000649097.1:c.925G>T ENSP00000497551.1:p.Ala309Ser
ENST00000649116.1:c.*482G>T ENSP00000497925.1:n.*482G>T
ENST00000649181.1:c.*287G>T ENSP00000498150.1:n.*287G>T
ENST00000649242.1:c.*610G>T ENSP00000497943.1:n.*610G>T
ENST00000649274.1:c.863G>T ENSP00000497032.1:n.863G>T
ENST00000649518.1:c.*529G>T ENSP00000498169.1:n.*529G>T
ENST00000649543.1:c.*529G>T ENSP00000496826.1:n.*529G>T
ENST00000649752.1:c.652G>T ENSP00000497267.1:p.Ala218Ser
ENST00000650076.1:c.211+26849G>T
ENST00000650471.1:c.*369G>T ENSP00000498027.1:n.*369G>T
ENST00000650604.1:c.352G>T ENSP00000497105.1:p.Ala118Ser
XM_011530986.1:c.925G>T XP_011529288.1:p.Ala309Ser
XM_011530986.3:c.925G>T XP_011529288.3:p.Ala309Ser
XM_011530987.1:c.925G>T XP_011529289.1:p.Ala309Ser
XM_011530988.1:c.925G>T XP_011529290.1:p.Ala309Ser
XM_017029640.2:c.847G>T XP_016885129.2:p.Ala283Ser
XM_017029641.2:c.847G>T XP_016885130.2:p.Ala283Ser
XM_017029642.1:c.766G>T XP_016885131.1:p.Ala256Ser
XM_017029643.2:c.739G>T XP_016885132.1:p.Ala247Ser
XM_017029644.2:c.688G>T XP_016885133.1:p.Ala230Ser
XM_017029645.2:c.739G>T XP_016885134.1:p.Ala247Ser
XM_017029646.1:c.538G>T XP_016885135.1:p.Ala180Ser
XM_024452405.1:c.340G>T XP_024308173.1:p.Ala114Ser
XR_001755711.2:n.1011G>T
XR_002958779.1:n.1011G>T
XR_002958780.1:n.1015G>T
XR_002958781.1:n.1015G>T
XR_002958782.1:n.3184G>T
XR_002958783.1:n.991G>T
XR_938402.1:n.1011G>T
XR_938402.3:n.1011G>T