Canonical Allele Identifier: CA413638535
Gene: HDAC8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72351825T>C , CM000685.2:g.72351825T>C GRCh38
NC_000023.10:g.71571675T>C , CM000685.1:g.71571675T>C GRCh37
NC_000023.9:g.71488400T>C NCBI36
NG_015851.1:g.226279A>G

Transcript Alleles

HGVS Amino-acid Change
NM_018486.3:c.1019A>G MANE Select NP_060956.1:p.Tyr340Cys
ENST00000373573.9:c.1019A>G MANE Select ENSP00000362674.3:p.Tyr340Cys
NM_001166418.1:c.746A>G NP_001159890.1:p.Tyr249Cys
NM_001166418.2:c.746A>G NP_001159890.1:p.Tyr249Cys
NM_018486.2:c.1019A>G NP_060956.1:p.Tyr340Cys
NR_051952.1:n.1219A>G
NR_051952.2:n.959A>G
ENST00000373568.7:c.1019A>G ENSP00000362669.3:p.Tyr340Cys
ENST00000373573.7:c.1019A>G ENSP00000362674.3:p.Tyr340Cys
ENST00000373583.5:c.165-22116A>G ENSP00000362685.1:n.165-22116A>G
ENST00000373583.6:c.941A>G ENSP00000362685.2:p.Tyr314Cys
ENST00000373589.8:c.746A>G ENSP00000362691.4:p.Tyr249Cys
ENST00000373589.9:c.746A>G ENSP00000362691.4:p.Tyr249Cys
ENST00000436675.6:c.*274A>G ENSP00000416489.1:n.*274A>G
ENST00000470998.1:n.192A>G
ENST00000470998.2:c.196A>G
ENST00000647594.1:c.1019A>G ENSP00000496814.1:p.Tyr340Cys
ENST00000647606.1:c.794A>G
ENST00000647613.1:c.*772A>G ENSP00000497911.1:n.*772A>G
ENST00000647641.1:n.1106A>G
ENST00000647654.1:c.746A>G ENSP00000497568.1:p.Tyr249Cys
ENST00000647859.1:c.1019A>G ENSP00000497530.1:p.Tyr340Cys
ENST00000647886.1:c.1019A>G ENSP00000497188.1:p.Tyr340Cys
ENST00000647980.1:c.1013A>G ENSP00000498002.1:p.Tyr338Cys
ENST00000648139.1:c.719A>G ENSP00000496818.1:p.Tyr240Cys
ENST00000648276.1:c.403A>G ENSP00000497619.1:p.Met135Val
ENST00000648452.1:c.1019A>G ENSP00000497268.1:p.Tyr340Cys
ENST00000648459.1:c.416A>G ENSP00000498072.1:p.Tyr139Cys
ENST00000648504.1:c.960A>G ENSP00000497668.1:n.960A>G
ENST00000648711.1:c.648A>G ENSP00000498040.1:n.648A>G
ENST00000648731.1:c.1125A>G
ENST00000648834.1:c.*99A>G ENSP00000497764.1:n.*99A>G
ENST00000648850.1:c.658A>G
ENST00000648855.1:n.943A>G
ENST00000648922.1:c.1019A>G ENSP00000497072.1:p.Tyr340Cys
ENST00000648939.1:c.*99A>G ENSP00000497442.1:n.*99A>G
ENST00000649097.1:c.1019A>G ENSP00000497551.1:p.Tyr340Cys
ENST00000649181.1:c.*381A>G ENSP00000498150.1:n.*381A>G
ENST00000649274.1:c.957A>G ENSP00000497032.1:n.957A>G
ENST00000649543.1:c.*623A>G ENSP00000496826.1:n.*623A>G
ENST00000650076.1:c.376A>G
ENST00000650471.1:c.*463A>G ENSP00000498027.1:n.*463A>G
ENST00000650604.1:c.446A>G ENSP00000497105.1:p.Tyr149Cys
XM_011530986.1:c.1019A>G XP_011529288.1:p.Tyr340Cys
XM_011530986.3:c.1019A>G XP_011529288.3:p.Tyr340Cys
XM_017029640.2:c.941A>G XP_016885129.2:p.Tyr314Cys
XM_017029641.2:c.941A>G XP_016885130.2:p.Tyr314Cys
XM_017029642.1:c.860A>G XP_016885131.1:p.Tyr287Cys
XM_017029643.2:c.833A>G XP_016885132.1:p.Tyr278Cys
XM_017029644.2:c.782A>G XP_016885133.1:p.Tyr261Cys
XM_017029645.2:c.833A>G XP_016885134.1:p.Tyr278Cys
XM_017029646.1:c.632A>G XP_016885135.1:p.Tyr211Cys
XM_024452405.1:c.434A>G XP_024308173.1:p.Tyr145Cys
XR_001755711.2:n.1105A>G
XR_002958779.1:n.1201A>G
XR_002958780.1:n.1109A>G
XR_002958781.1:n.1109A>G
XR_002958783.1:n.1085A>G
XR_938402.1:n.1105A>G
XR_938402.3:n.1105A>G