Canonical Allele Identifier: CA10450107

Gene: HDAC8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72351792C>G , CM000685.2:g.72351792C>G	GRCh38
NC_000023.10:g.71571642C>G , CM000685.1:g.71571642C>G	GRCh37
NC_000023.9:g.71488367C>G	NCBI36
NG_015851.1:g.226312G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.1052G>C	ENSP00000362669.3:p.Ser351Thr
ENST00000373573.9:c.1052G>C MANE Select	ENSP00000362674.3:p.Ser351Thr
ENST00000373583.6:c.974G>C	ENSP00000362685.2:p.Ser325Thr
ENST00000373589.9:c.779G>C	ENSP00000362691.4:p.Ser260Thr
ENST00000436675.6:c.*307G>C	ENSP00000416489.1:n.*307G>C
ENST00000470998.2:c.229G>C
ENST00000647594.1:c.1052G>C	ENSP00000496814.1:p.Ser351Thr
ENST00000647606.1:c.827G>C
ENST00000647613.1:c.*805G>C	ENSP00000497911.1:n.*805G>C
ENST00000647641.1:n.1139G>C
ENST00000647654.1:c.779G>C	ENSP00000497568.1:p.Ser260Thr
ENST00000647859.1:c.1052G>C	ENSP00000497530.1:p.Ser351Thr
ENST00000647886.1:c.1052G>C	ENSP00000497188.1:p.Ser351Thr
ENST00000647980.1:c.1046G>C	ENSP00000498002.1:p.Ser349Thr
ENST00000648139.1:c.752G>C	ENSP00000496818.1:p.Ser251Thr
ENST00000648276.1:c.436G>C	ENSP00000497619.1:p.Ala146Pro
ENST00000648452.1:c.1052G>C	ENSP00000497268.1:p.Ser351Thr
ENST00000648459.1:c.449G>C	ENSP00000498072.1:p.Ser150Thr
ENST00000648504.1:c.993G>C	ENSP00000497668.1:n.993G>C
ENST00000648711.1:c.681G>C	ENSP00000498040.1:n.681G>C
ENST00000648731.1:c.1158G>C
ENST00000648834.1:c.*132G>C	ENSP00000497764.1:n.*132G>C
ENST00000648850.1:c.691G>C
ENST00000648855.1:n.976G>C
ENST00000648922.1:c.1052G>C	ENSP00000497072.1:p.Ser351Thr
ENST00000648939.1:c.*132G>C	ENSP00000497442.1:n.*132G>C
ENST00000649097.1:c.1052G>C	ENSP00000497551.1:p.Ser351Thr
ENST00000649181.1:c.*414G>C	ENSP00000498150.1:n.*414G>C
ENST00000649274.1:c.990G>C	ENSP00000497032.1:n.990G>C
ENST00000649543.1:c.*656G>C	ENSP00000496826.1:n.*656G>C
ENST00000650076.1:c.409G>C
ENST00000650471.1:c.*496G>C	ENSP00000498027.1:n.*496G>C
ENST00000650604.1:c.479G>C	ENSP00000497105.1:p.Ser160Thr
ENST00000373573.7:c.1052G>C	ENSP00000362674.3:p.Ser351Thr
ENST00000373583.5:c.165-22083G>C	ENSP00000362685.1:n.165-22083G>C
ENST00000373589.8:c.779G>C	ENSP00000362691.4:p.Ser260Thr
ENST00000470998.1:n.225G>C
NM_001166418.1:c.779G>C	NP_001159890.1:p.Ser260Thr
NM_018486.2:c.1052G>C	NP_060956.1:p.Ser351Thr
NR_051952.1:n.1252G>C
XM_011530986.1:c.1052G>C	XP_011529288.1:p.Ser351Thr
XR_938402.1:n.1138G>C
XM_011530986.3:c.1052G>C	XP_011529288.3:p.Ser351Thr
XM_017029640.2:c.974G>C	XP_016885129.2:p.Ser325Thr
XM_017029641.2:c.974G>C	XP_016885130.2:p.Ser325Thr
XM_017029642.1:c.893G>C	XP_016885131.1:p.Ser298Thr
XM_017029643.2:c.866G>C	XP_016885132.1:p.Ser289Thr
XM_017029644.2:c.815G>C	XP_016885133.1:p.Ser272Thr
XM_017029645.2:c.866G>C	XP_016885134.1:p.Ser289Thr
XM_017029646.1:c.665G>C	XP_016885135.1:p.Ser222Thr
XM_024452405.1:c.467G>C	XP_024308173.1:p.Ser156Thr
XR_001755711.2:n.1138G>C
XR_002958779.1:n.1234G>C
XR_002958780.1:n.1142G>C
XR_002958781.1:n.1142G>C
XR_002958783.1:n.1118G>C
XR_938402.3:n.1138G>C
NM_018486.3:c.1052G>C MANE Select	NP_060956.1:p.Ser351Thr
NM_001166418.2:c.779G>C	NP_001159890.1:p.Ser260Thr
NR_051952.2:n.992G>C