Canonical Allele Identifier: CA413643004

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684481T>A (hg19) ; chrX:g.72464631T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464631T>A , CM000685.2:g.72464631T>A	GRCh38
NC_000023.10:g.71684481T>A , CM000685.1:g.71684481T>A	GRCh37
NC_000023.9:g.71601206T>A	NCBI36
NG_015851.1:g.113473A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.838A>T	ENSP00000362669.3:p.Thr280Ser
ENST00000373573.9:c.838A>T MANE Select	ENSP00000362674.3:p.Thr280Ser
ENST00000373583.6:c.760A>T	ENSP00000362685.2:p.Thr254Ser
ENST00000373589.9:c.565A>T	ENSP00000362691.4:p.Thr189Ser
ENST00000415409.6:c.838A>T	ENSP00000396424.2:p.Thr280Ser
ENST00000436675.6:c.*93A>T	ENSP00000416489.1:n.*93A>T
ENST00000478743.2:n.924A>T
ENST00000647594.1:c.838A>T	ENSP00000496814.1:p.Thr280Ser
ENST00000647606.1:c.613A>T
ENST00000647613.1:c.*591A>T	ENSP00000497911.1:n.*591A>T
ENST00000647641.1:n.925A>T
ENST00000647654.1:c.565A>T	ENSP00000497568.1:p.Thr189Ser
ENST00000647718.1:n.893A>T
ENST00000647859.1:c.838A>T	ENSP00000497530.1:p.Thr280Ser
ENST00000647886.1:c.838A>T	ENSP00000497188.1:p.Thr280Ser
ENST00000647980.1:c.832A>T	ENSP00000498002.1:p.Thr278Ser
ENST00000648139.1:c.538A>T	ENSP00000496818.1:p.Thr180Ser
ENST00000648276.1:c.82A>T	ENSP00000497619.1:p.Thr28Ser
ENST00000648285.1:n.621A>T
ENST00000648298.1:c.838A>T	ENSP00000496866.1:p.Thr280Ser
ENST00000648452.1:c.838A>T	ENSP00000497268.1:p.Thr280Ser
ENST00000648459.1:c.235A>T	ENSP00000498072.1:p.Thr79Ser
ENST00000648504.1:c.775A>T	ENSP00000497668.1:p.Thr259Ser
ENST00000648711.1:c.463A>T	ENSP00000498040.1:p.Thr155Ser
ENST00000648731.1:c.944A>T
ENST00000648834.1:c.838A>T	ENSP00000497764.1:p.Thr280Ser
ENST00000648850.1:c.473A>T
ENST00000648855.1:n.762A>T
ENST00000648870.1:c.838A>T	ENSP00000497599.1:p.Thr280Ser
ENST00000648922.1:c.838A>T	ENSP00000497072.1:p.Thr280Ser
ENST00000648939.1:c.838A>T	ENSP00000497442.1:p.Thr280Ser
ENST00000649097.1:c.838A>T	ENSP00000497551.1:p.Thr280Ser
ENST00000649116.1:c.*395A>T	ENSP00000497925.1:n.*395A>T
ENST00000649181.1:c.*200A>T	ENSP00000498150.1:n.*200A>T
ENST00000649242.1:c.*442A>T	ENSP00000497943.1:n.*442A>T
ENST00000649274.1:c.776A>T	ENSP00000497032.1:n.776A>T
ENST00000649518.1:c.*442A>T	ENSP00000498169.1:n.*442A>T
ENST00000649543.1:c.*442A>T	ENSP00000496826.1:n.*442A>T
ENST00000649752.1:c.565A>T	ENSP00000497267.1:p.Thr189Ser
ENST00000650076.1:c.211+24302A>T
ENST00000650471.1:c.*282A>T	ENSP00000498027.1:n.*282A>T
ENST00000650604.1:c.265A>T	ENSP00000497105.1:p.Thr89Ser
ENST00000373568.6:c.565A>T	ENSP00000362669.2:p.Thr189Ser
ENST00000373573.7:c.838A>T	ENSP00000362674.3:p.Thr280Ser
ENST00000373583.5:c.164+107426A>T	ENSP00000362685.1:n.164+107426A>T
ENST00000373589.8:c.565A>T	ENSP00000362691.4:p.Thr189Ser
ENST00000415409.5:c.760A>T	ENSP00000396424.1:p.Thr254Ser
ENST00000436675.5:c.*93A>T	ENSP00000416489.1:n.*93A>T
NM_001166418.1:c.565A>T	NP_001159890.1:p.Thr189Ser
NM_018486.2:c.838A>T	NP_060956.1:p.Thr280Ser
NR_051952.1:n.1038A>T
XM_011530986.1:c.838A>T	XP_011529288.1:p.Thr280Ser
XM_011530987.1:c.838A>T	XP_011529289.1:p.Thr280Ser
XM_011530988.1:c.838A>T	XP_011529290.1:p.Thr280Ser
XR_938402.1:n.924A>T
XM_011530986.3:c.838A>T	XP_011529288.3:p.Thr280Ser
XM_017029640.2:c.760A>T	XP_016885129.2:p.Thr254Ser
XM_017029641.2:c.760A>T	XP_016885130.2:p.Thr254Ser
XM_017029642.1:c.679A>T	XP_016885131.1:p.Thr227Ser
XM_017029643.2:c.652A>T	XP_016885132.1:p.Thr218Ser
XM_017029644.2:c.601A>T	XP_016885133.1:p.Thr201Ser
XM_017029645.2:c.652A>T	XP_016885134.1:p.Thr218Ser
XM_017029646.1:c.451A>T	XP_016885135.1:p.Thr151Ser
XM_024452405.1:c.253A>T	XP_024308173.1:p.Thr85Ser
XR_001755711.2:n.924A>T
XR_002958779.1:n.924A>T
XR_002958780.1:n.924A>T
XR_002958781.1:n.924A>T
XR_002958782.1:n.900A>T
XR_002958783.1:n.900A>T
XR_938402.3:n.924A>T
NM_018486.3:c.838A>T MANE Select	NP_060956.1:p.Thr280Ser
NM_001166418.2:c.565A>T	NP_001159890.1:p.Thr189Ser
NR_051952.2:n.778A>T