Canonical Allele Identifier: CA413642749

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684426G>A (hg19) ; chrX:g.72464576G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464576G>A , CM000685.2:g.72464576G>A	GRCh38
NC_000023.10:g.71684426G>A , CM000685.1:g.71684426G>A	GRCh37
NC_000023.9:g.71601151G>A	NCBI36
NG_015851.1:g.113528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.893C>T	ENSP00000362669.3:p.Thr298Ile
ENST00000373573.9:c.893C>T MANE Select	ENSP00000362674.3:p.Thr298Ile
ENST00000373583.6:c.815C>T	ENSP00000362685.2:p.Thr272Ile
ENST00000373589.9:c.620C>T	ENSP00000362691.4:p.Thr207Ile
ENST00000415409.6:c.893C>T	ENSP00000396424.2:p.Thr298Ile
ENST00000436675.6:c.*148C>T	ENSP00000416489.1:n.*148C>T
ENST00000478743.2:n.979C>T
ENST00000647594.1:c.893C>T	ENSP00000496814.1:p.Thr298Ile
ENST00000647606.1:c.668C>T
ENST00000647613.1:c.*646C>T	ENSP00000497911.1:n.*646C>T
ENST00000647641.1:n.980C>T
ENST00000647654.1:c.620C>T	ENSP00000497568.1:p.Thr207Ile
ENST00000647718.1:n.948C>T
ENST00000647859.1:c.893C>T	ENSP00000497530.1:p.Thr298Ile
ENST00000647886.1:c.893C>T	ENSP00000497188.1:p.Thr298Ile
ENST00000647980.1:c.887C>T	ENSP00000498002.1:p.Thr296Ile
ENST00000648139.1:c.593C>T	ENSP00000496818.1:p.Thr198Ile
ENST00000648276.1:c.137C>T	ENSP00000497619.1:p.Thr46Ile
ENST00000648285.1:n.676C>T
ENST00000648298.1:c.893C>T	ENSP00000496866.1:p.Thr298Ile
ENST00000648452.1:c.893C>T	ENSP00000497268.1:p.Thr298Ile
ENST00000648459.1:c.290C>T	ENSP00000498072.1:p.Thr97Ile
ENST00000648504.1:c.830C>T	ENSP00000497668.1:p.Thr277Ile
ENST00000648711.1:c.518C>T	ENSP00000498040.1:p.Thr173Ile
ENST00000648731.1:c.999C>T
ENST00000648834.1:c.893C>T	ENSP00000497764.1:p.Thr298Ile
ENST00000648850.1:c.528C>T
ENST00000648855.1:n.817C>T
ENST00000648870.1:c.893C>T	ENSP00000497599.1:p.Thr298Ile
ENST00000648922.1:c.893C>T	ENSP00000497072.1:p.Thr298Ile
ENST00000648939.1:c.893C>T	ENSP00000497442.1:p.Thr298Ile
ENST00000649097.1:c.893C>T	ENSP00000497551.1:p.Thr298Ile
ENST00000649116.1:c.*450C>T	ENSP00000497925.1:n.*450C>T
ENST00000649181.1:c.*255C>T	ENSP00000498150.1:n.*255C>T
ENST00000649242.1:c.*497C>T	ENSP00000497943.1:n.*497C>T
ENST00000649274.1:c.831C>T	ENSP00000497032.1:n.831C>T
ENST00000649518.1:c.*497C>T	ENSP00000498169.1:n.*497C>T
ENST00000649543.1:c.*497C>T	ENSP00000496826.1:n.*497C>T
ENST00000649752.1:c.620C>T	ENSP00000497267.1:p.Thr207Ile
ENST00000650076.1:c.211+24357C>T
ENST00000650471.1:c.*337C>T	ENSP00000498027.1:n.*337C>T
ENST00000650604.1:c.320C>T	ENSP00000497105.1:p.Thr107Ile
ENST00000373568.6:c.620C>T	ENSP00000362669.2:p.Thr207Ile
ENST00000373573.7:c.893C>T	ENSP00000362674.3:p.Thr298Ile
ENST00000373583.5:c.164+107481C>T	ENSP00000362685.1:n.164+107481C>T
ENST00000373589.8:c.620C>T	ENSP00000362691.4:p.Thr207Ile
ENST00000415409.5:c.815C>T	ENSP00000396424.1:p.Thr272Ile
ENST00000436675.5:c.*148C>T	ENSP00000416489.1:n.*148C>T
NM_001166418.1:c.620C>T	NP_001159890.1:p.Thr207Ile
NM_018486.2:c.893C>T	NP_060956.1:p.Thr298Ile
NR_051952.1:n.1093C>T
XM_011530986.1:c.893C>T	XP_011529288.1:p.Thr298Ile
XM_011530987.1:c.893C>T	XP_011529289.1:p.Thr298Ile
XM_011530988.1:c.893C>T	XP_011529290.1:p.Thr298Ile
XR_938402.1:n.979C>T
XM_011530986.3:c.893C>T	XP_011529288.3:p.Thr298Ile
XM_017029640.2:c.815C>T	XP_016885129.2:p.Thr272Ile
XM_017029641.2:c.815C>T	XP_016885130.2:p.Thr272Ile
XM_017029642.1:c.734C>T	XP_016885131.1:p.Thr245Ile
XM_017029643.2:c.707C>T	XP_016885132.1:p.Thr236Ile
XM_017029644.2:c.656C>T	XP_016885133.1:p.Thr219Ile
XM_017029645.2:c.707C>T	XP_016885134.1:p.Thr236Ile
XM_017029646.1:c.506C>T	XP_016885135.1:p.Thr169Ile
XM_024452405.1:c.308C>T	XP_024308173.1:p.Thr103Ile
XR_001755711.2:n.979C>T
XR_002958779.1:n.979C>T
XR_002958780.1:n.979C>T
XR_002958781.1:n.979C>T
XR_002958782.1:n.955C>T
XR_002958783.1:n.955C>T
XR_938402.3:n.979C>T
NM_018486.3:c.893C>T MANE Select	NP_060956.1:p.Thr298Ile
NM_001166418.2:c.620C>T	NP_001159890.1:p.Thr207Ile
NR_051952.2:n.833C>T