Canonical Allele Identifier: CA516779389

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684491G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464641G>T , CM000685.2:g.72464641G>T	GRCh38
NC_000023.10:g.71684491G>T , CM000685.1:g.71684491G>T	GRCh37
NC_000023.9:g.71601216G>T	NCBI36
NG_015851.1:g.113463C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.828C>A	ENSP00000362669.3:p.Ser276=
ENST00000373573.9:c.828C>A MANE Select	ENSP00000362674.3:p.Ser276=
ENST00000373583.6:c.750C>A	ENSP00000362685.2:p.Ser250=
ENST00000373589.9:c.555C>A	ENSP00000362691.4:p.Ser185=
ENST00000415409.6:c.828C>A	ENSP00000396424.2:p.Ser276=
ENST00000436675.6:c.*83C>A	ENSP00000416489.1:n.*83C>A
ENST00000478743.2:n.914C>A
ENST00000647594.1:c.828C>A	ENSP00000496814.1:p.Ser276=
ENST00000647606.1:c.603C>A
ENST00000647613.1:c.*581C>A	ENSP00000497911.1:n.*581C>A
ENST00000647641.1:n.915C>A
ENST00000647654.1:c.555C>A	ENSP00000497568.1:p.Ser185=
ENST00000647718.1:n.883C>A
ENST00000647859.1:c.828C>A	ENSP00000497530.1:p.Ser276=
ENST00000647886.1:c.828C>A	ENSP00000497188.1:p.Ser276=
ENST00000647980.1:c.822C>A	ENSP00000498002.1:p.Ser274=
ENST00000648139.1:c.528C>A	ENSP00000496818.1:p.Ser176=
ENST00000648276.1:c.72C>A	ENSP00000497619.1:p.Ser24=
ENST00000648285.1:n.611C>A
ENST00000648298.1:c.828C>A	ENSP00000496866.1:p.Ser276=
ENST00000648452.1:c.828C>A	ENSP00000497268.1:p.Ser276=
ENST00000648459.1:c.225C>A	ENSP00000498072.1:p.Ser75=
ENST00000648504.1:c.765C>A	ENSP00000497668.1:p.Ser255=
ENST00000648711.1:c.453C>A	ENSP00000498040.1:p.Ser151=
ENST00000648731.1:c.934C>A
ENST00000648834.1:c.828C>A	ENSP00000497764.1:p.Ser276=
ENST00000648850.1:c.463C>A
ENST00000648855.1:n.752C>A
ENST00000648870.1:c.828C>A	ENSP00000497599.1:p.Ser276=
ENST00000648922.1:c.828C>A	ENSP00000497072.1:p.Ser276=
ENST00000648939.1:c.828C>A	ENSP00000497442.1:p.Ser276=
ENST00000649097.1:c.828C>A	ENSP00000497551.1:p.Ser276=
ENST00000649116.1:c.*385C>A	ENSP00000497925.1:n.*385C>A
ENST00000649181.1:c.*190C>A	ENSP00000498150.1:n.*190C>A
ENST00000649242.1:c.*432C>A	ENSP00000497943.1:n.*432C>A
ENST00000649274.1:c.766C>A	ENSP00000497032.1:n.766C>A
ENST00000649518.1:c.*432C>A	ENSP00000498169.1:n.*432C>A
ENST00000649543.1:c.*432C>A	ENSP00000496826.1:n.*432C>A
ENST00000649752.1:c.555C>A	ENSP00000497267.1:p.Ser185=
ENST00000650076.1:c.211+24292C>A
ENST00000650471.1:c.*272C>A	ENSP00000498027.1:n.*272C>A
ENST00000650604.1:c.255C>A	ENSP00000497105.1:p.Ser85=
ENST00000373568.6:c.555C>A	ENSP00000362669.2:p.Ser185=
ENST00000373573.7:c.828C>A	ENSP00000362674.3:p.Ser276=
ENST00000373583.5:c.164+107416C>A	ENSP00000362685.1:n.164+107416C>A
ENST00000373589.8:c.555C>A	ENSP00000362691.4:p.Ser185=
ENST00000415409.5:c.750C>A	ENSP00000396424.1:p.Ser250=
ENST00000436675.5:c.*83C>A	ENSP00000416489.1:n.*83C>A
NM_001166418.1:c.555C>A	NP_001159890.1:p.Ser185=
NM_018486.2:c.828C>A	NP_060956.1:p.Ser276=
NR_051952.1:n.1028C>A
XM_011530986.1:c.828C>A	XP_011529288.1:p.Ser276=
XM_011530987.1:c.828C>A	XP_011529289.1:p.Ser276=
XM_011530988.1:c.828C>A	XP_011529290.1:p.Ser276=
XR_938402.1:n.914C>A
XM_011530986.3:c.828C>A	XP_011529288.3:p.Ser276=
XM_017029640.2:c.750C>A	XP_016885129.2:p.Ser250=
XM_017029641.2:c.750C>A	XP_016885130.2:p.Ser250=
XM_017029642.1:c.669C>A	XP_016885131.1:p.Ser223=
XM_017029643.2:c.642C>A	XP_016885132.1:p.Ser214=
XM_017029644.2:c.591C>A	XP_016885133.1:p.Ser197=
XM_017029645.2:c.642C>A	XP_016885134.1:p.Ser214=
XM_017029646.1:c.441C>A	XP_016885135.1:p.Ser147=
XM_024452405.1:c.243C>A	XP_024308173.1:p.Ser81=
XR_001755711.2:n.914C>A
XR_002958779.1:n.914C>A
XR_002958780.1:n.914C>A
XR_002958781.1:n.914C>A
XR_002958782.1:n.890C>A
XR_002958783.1:n.890C>A
XR_938402.3:n.914C>A
NM_018486.3:c.828C>A MANE Select	NP_060956.1:p.Ser276=
NM_001166418.2:c.555C>A	NP_001159890.1:p.Ser185=
NR_051952.2:n.768C>A