Canonical Allele Identifier: CA413643167

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684517T>G (hg19) ; chrX:g.72464667T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464667T>G , CM000685.2:g.72464667T>G	GRCh38
NC_000023.10:g.71684517T>G , CM000685.1:g.71684517T>G	GRCh37
NC_000023.9:g.71601242T>G	NCBI36
NG_015851.1:g.113437A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.802A>C	ENSP00000362669.3:p.Thr268Pro
ENST00000373573.9:c.802A>C MANE Select	ENSP00000362674.3:p.Thr268Pro
ENST00000373583.6:c.724A>C	ENSP00000362685.2:p.Thr242Pro
ENST00000373589.9:c.529A>C	ENSP00000362691.4:p.Thr177Pro
ENST00000415409.6:c.802A>C	ENSP00000396424.2:p.Thr268Pro
ENST00000436675.6:c.*57A>C	ENSP00000416489.1:n.*57A>C
ENST00000478743.2:n.888A>C
ENST00000647594.1:c.802A>C	ENSP00000496814.1:p.Thr268Pro
ENST00000647606.1:c.577A>C
ENST00000647613.1:c.*555A>C	ENSP00000497911.1:n.*555A>C
ENST00000647641.1:n.889A>C
ENST00000647654.1:c.529A>C	ENSP00000497568.1:p.Thr177Pro
ENST00000647718.1:n.857A>C
ENST00000647859.1:c.802A>C	ENSP00000497530.1:p.Thr268Pro
ENST00000647886.1:c.802A>C	ENSP00000497188.1:p.Thr268Pro
ENST00000647980.1:c.796A>C	ENSP00000498002.1:p.Thr266Pro
ENST00000648139.1:c.502A>C	ENSP00000496818.1:p.Thr168Pro
ENST00000648276.1:c.46A>C	ENSP00000497619.1:p.Thr16Pro
ENST00000648285.1:n.585A>C
ENST00000648298.1:c.802A>C	ENSP00000496866.1:p.Thr268Pro
ENST00000648452.1:c.802A>C	ENSP00000497268.1:p.Thr268Pro
ENST00000648459.1:c.199A>C	ENSP00000498072.1:p.Thr67Pro
ENST00000648504.1:c.739A>C	ENSP00000497668.1:p.Thr247Pro
ENST00000648711.1:c.427A>C	ENSP00000498040.1:p.Thr143Pro
ENST00000648731.1:c.908A>C
ENST00000648834.1:c.802A>C	ENSP00000497764.1:p.Thr268Pro
ENST00000648850.1:c.437A>C
ENST00000648855.1:n.726A>C
ENST00000648870.1:c.802A>C	ENSP00000497599.1:p.Thr268Pro
ENST00000648922.1:c.802A>C	ENSP00000497072.1:p.Thr268Pro
ENST00000648939.1:c.802A>C	ENSP00000497442.1:p.Thr268Pro
ENST00000649097.1:c.802A>C	ENSP00000497551.1:p.Thr268Pro
ENST00000649116.1:c.*359A>C	ENSP00000497925.1:n.*359A>C
ENST00000649181.1:c.*164A>C	ENSP00000498150.1:n.*164A>C
ENST00000649242.1:c.*406A>C	ENSP00000497943.1:n.*406A>C
ENST00000649274.1:c.740A>C	ENSP00000497032.1:n.740A>C
ENST00000649518.1:c.*406A>C	ENSP00000498169.1:n.*406A>C
ENST00000649543.1:c.*406A>C	ENSP00000496826.1:n.*406A>C
ENST00000649752.1:c.529A>C	ENSP00000497267.1:p.Thr177Pro
ENST00000650076.1:c.211+24266A>C
ENST00000650471.1:c.*246A>C	ENSP00000498027.1:n.*246A>C
ENST00000650604.1:c.229A>C	ENSP00000497105.1:p.Thr77Pro
ENST00000373568.6:c.529A>C	ENSP00000362669.2:p.Thr177Pro
ENST00000373573.7:c.802A>C	ENSP00000362674.3:p.Thr268Pro
ENST00000373583.5:c.164+107390A>C	ENSP00000362685.1:n.164+107390A>C
ENST00000373589.8:c.529A>C	ENSP00000362691.4:p.Thr177Pro
ENST00000415409.5:c.724A>C	ENSP00000396424.1:p.Thr242Pro
ENST00000436675.5:c.*57A>C	ENSP00000416489.1:n.*57A>C
NM_001166418.1:c.529A>C	NP_001159890.1:p.Thr177Pro
NM_018486.2:c.802A>C	NP_060956.1:p.Thr268Pro
NR_051952.1:n.1002A>C
XM_011530986.1:c.802A>C	XP_011529288.1:p.Thr268Pro
XM_011530987.1:c.802A>C	XP_011529289.1:p.Thr268Pro
XM_011530988.1:c.802A>C	XP_011529290.1:p.Thr268Pro
XR_938402.1:n.888A>C
XM_011530986.3:c.802A>C	XP_011529288.3:p.Thr268Pro
XM_017029640.2:c.724A>C	XP_016885129.2:p.Thr242Pro
XM_017029641.2:c.724A>C	XP_016885130.2:p.Thr242Pro
XM_017029642.1:c.643A>C	XP_016885131.1:p.Thr215Pro
XM_017029643.2:c.616A>C	XP_016885132.1:p.Thr206Pro
XM_017029644.2:c.565A>C	XP_016885133.1:p.Thr189Pro
XM_017029645.2:c.616A>C	XP_016885134.1:p.Thr206Pro
XM_017029646.1:c.415A>C	XP_016885135.1:p.Thr139Pro
XM_024452405.1:c.217A>C	XP_024308173.1:p.Thr73Pro
XR_001755711.2:n.888A>C
XR_002958779.1:n.888A>C
XR_002958780.1:n.888A>C
XR_002958781.1:n.888A>C
XR_002958782.1:n.864A>C
XR_002958783.1:n.864A>C
XR_938402.3:n.888A>C
NM_018486.3:c.802A>C MANE Select	NP_060956.1:p.Thr268Pro
NM_001166418.2:c.529A>C	NP_001159890.1:p.Thr177Pro
NR_051952.2:n.742A>C