Canonical Allele Identifier: CA413643161

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684516G>C (hg19) ; chrX:g.72464666G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464666G>C , CM000685.2:g.72464666G>C	GRCh38
NC_000023.10:g.71684516G>C , CM000685.1:g.71684516G>C	GRCh37
NC_000023.9:g.71601241G>C	NCBI36
NG_015851.1:g.113438C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.803C>G	ENSP00000362669.3:p.Thr268Arg
ENST00000373573.9:c.803C>G MANE Select	ENSP00000362674.3:p.Thr268Arg
ENST00000373583.6:c.725C>G	ENSP00000362685.2:p.Thr242Arg
ENST00000373589.9:c.530C>G	ENSP00000362691.4:p.Thr177Arg
ENST00000415409.6:c.803C>G	ENSP00000396424.2:p.Thr268Arg
ENST00000436675.6:c.*58C>G	ENSP00000416489.1:n.*58C>G
ENST00000478743.2:n.889C>G
ENST00000647594.1:c.803C>G	ENSP00000496814.1:p.Thr268Arg
ENST00000647606.1:c.578C>G
ENST00000647613.1:c.*556C>G	ENSP00000497911.1:n.*556C>G
ENST00000647641.1:n.890C>G
ENST00000647654.1:c.530C>G	ENSP00000497568.1:p.Thr177Arg
ENST00000647718.1:n.858C>G
ENST00000647859.1:c.803C>G	ENSP00000497530.1:p.Thr268Arg
ENST00000647886.1:c.803C>G	ENSP00000497188.1:p.Thr268Arg
ENST00000647980.1:c.797C>G	ENSP00000498002.1:p.Thr266Arg
ENST00000648139.1:c.503C>G	ENSP00000496818.1:p.Thr168Arg
ENST00000648276.1:c.47C>G	ENSP00000497619.1:p.Thr16Arg
ENST00000648285.1:n.586C>G
ENST00000648298.1:c.803C>G	ENSP00000496866.1:p.Thr268Arg
ENST00000648452.1:c.803C>G	ENSP00000497268.1:p.Thr268Arg
ENST00000648459.1:c.200C>G	ENSP00000498072.1:p.Thr67Arg
ENST00000648504.1:c.740C>G	ENSP00000497668.1:p.Thr247Arg
ENST00000648711.1:c.428C>G	ENSP00000498040.1:p.Thr143Arg
ENST00000648731.1:c.909C>G
ENST00000648834.1:c.803C>G	ENSP00000497764.1:p.Thr268Arg
ENST00000648850.1:c.438C>G
ENST00000648855.1:n.727C>G
ENST00000648870.1:c.803C>G	ENSP00000497599.1:p.Thr268Arg
ENST00000648922.1:c.803C>G	ENSP00000497072.1:p.Thr268Arg
ENST00000648939.1:c.803C>G	ENSP00000497442.1:p.Thr268Arg
ENST00000649097.1:c.803C>G	ENSP00000497551.1:p.Thr268Arg
ENST00000649116.1:c.*360C>G	ENSP00000497925.1:n.*360C>G
ENST00000649181.1:c.*165C>G	ENSP00000498150.1:n.*165C>G
ENST00000649242.1:c.*407C>G	ENSP00000497943.1:n.*407C>G
ENST00000649274.1:c.741C>G	ENSP00000497032.1:n.741C>G
ENST00000649518.1:c.*407C>G	ENSP00000498169.1:n.*407C>G
ENST00000649543.1:c.*407C>G	ENSP00000496826.1:n.*407C>G
ENST00000649752.1:c.530C>G	ENSP00000497267.1:p.Thr177Arg
ENST00000650076.1:c.211+24267C>G
ENST00000650471.1:c.*247C>G	ENSP00000498027.1:n.*247C>G
ENST00000650604.1:c.230C>G	ENSP00000497105.1:p.Thr77Arg
ENST00000373568.6:c.530C>G	ENSP00000362669.2:p.Thr177Arg
ENST00000373573.7:c.803C>G	ENSP00000362674.3:p.Thr268Arg
ENST00000373583.5:c.164+107391C>G	ENSP00000362685.1:n.164+107391C>G
ENST00000373589.8:c.530C>G	ENSP00000362691.4:p.Thr177Arg
ENST00000415409.5:c.725C>G	ENSP00000396424.1:p.Thr242Arg
ENST00000436675.5:c.*58C>G	ENSP00000416489.1:n.*58C>G
NM_001166418.1:c.530C>G	NP_001159890.1:p.Thr177Arg
NM_018486.2:c.803C>G	NP_060956.1:p.Thr268Arg
NR_051952.1:n.1003C>G
XM_011530986.1:c.803C>G	XP_011529288.1:p.Thr268Arg
XM_011530987.1:c.803C>G	XP_011529289.1:p.Thr268Arg
XM_011530988.1:c.803C>G	XP_011529290.1:p.Thr268Arg
XR_938402.1:n.889C>G
XM_011530986.3:c.803C>G	XP_011529288.3:p.Thr268Arg
XM_017029640.2:c.725C>G	XP_016885129.2:p.Thr242Arg
XM_017029641.2:c.725C>G	XP_016885130.2:p.Thr242Arg
XM_017029642.1:c.644C>G	XP_016885131.1:p.Thr215Arg
XM_017029643.2:c.617C>G	XP_016885132.1:p.Thr206Arg
XM_017029644.2:c.566C>G	XP_016885133.1:p.Thr189Arg
XM_017029645.2:c.617C>G	XP_016885134.1:p.Thr206Arg
XM_017029646.1:c.416C>G	XP_016885135.1:p.Thr139Arg
XM_024452405.1:c.218C>G	XP_024308173.1:p.Thr73Arg
XR_001755711.2:n.889C>G
XR_002958779.1:n.889C>G
XR_002958780.1:n.889C>G
XR_002958781.1:n.889C>G
XR_002958782.1:n.865C>G
XR_002958783.1:n.865C>G
XR_938402.3:n.889C>G
NM_018486.3:c.803C>G MANE Select	NP_060956.1:p.Thr268Arg
NM_001166418.2:c.530C>G	NP_001159890.1:p.Thr177Arg
NR_051952.2:n.743C>G