Canonical Allele Identifier: CA413643053

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684492G>T (hg19) ; chrX:g.72464642G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464642G>T , CM000685.2:g.72464642G>T	GRCh38
NC_000023.10:g.71684492G>T , CM000685.1:g.71684492G>T	GRCh37
NC_000023.9:g.71601217G>T	NCBI36
NG_015851.1:g.113462C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.827C>A	ENSP00000362669.3:p.Ser276Tyr
ENST00000373573.9:c.827C>A MANE Select	ENSP00000362674.3:p.Ser276Tyr
ENST00000373583.6:c.749C>A	ENSP00000362685.2:p.Ser250Tyr
ENST00000373589.9:c.554C>A	ENSP00000362691.4:p.Ser185Tyr
ENST00000415409.6:c.827C>A	ENSP00000396424.2:p.Ser276Tyr
ENST00000436675.6:c.*82C>A	ENSP00000416489.1:n.*82C>A
ENST00000478743.2:n.913C>A
ENST00000647594.1:c.827C>A	ENSP00000496814.1:p.Ser276Tyr
ENST00000647606.1:c.602C>A
ENST00000647613.1:c.*580C>A	ENSP00000497911.1:n.*580C>A
ENST00000647641.1:n.914C>A
ENST00000647654.1:c.554C>A	ENSP00000497568.1:p.Ser185Tyr
ENST00000647718.1:n.882C>A
ENST00000647859.1:c.827C>A	ENSP00000497530.1:p.Ser276Tyr
ENST00000647886.1:c.827C>A	ENSP00000497188.1:p.Ser276Tyr
ENST00000647980.1:c.821C>A	ENSP00000498002.1:p.Ser274Tyr
ENST00000648139.1:c.527C>A	ENSP00000496818.1:p.Ser176Tyr
ENST00000648276.1:c.71C>A	ENSP00000497619.1:p.Ser24Tyr
ENST00000648285.1:n.610C>A
ENST00000648298.1:c.827C>A	ENSP00000496866.1:p.Ser276Tyr
ENST00000648452.1:c.827C>A	ENSP00000497268.1:p.Ser276Tyr
ENST00000648459.1:c.224C>A	ENSP00000498072.1:p.Ser75Tyr
ENST00000648504.1:c.764C>A	ENSP00000497668.1:p.Ser255Tyr
ENST00000648711.1:c.452C>A	ENSP00000498040.1:p.Ser151Tyr
ENST00000648731.1:c.933C>A
ENST00000648834.1:c.827C>A	ENSP00000497764.1:p.Ser276Tyr
ENST00000648850.1:c.462C>A
ENST00000648855.1:n.751C>A
ENST00000648870.1:c.827C>A	ENSP00000497599.1:p.Ser276Tyr
ENST00000648922.1:c.827C>A	ENSP00000497072.1:p.Ser276Tyr
ENST00000648939.1:c.827C>A	ENSP00000497442.1:p.Ser276Tyr
ENST00000649097.1:c.827C>A	ENSP00000497551.1:p.Ser276Tyr
ENST00000649116.1:c.*384C>A	ENSP00000497925.1:n.*384C>A
ENST00000649181.1:c.*189C>A	ENSP00000498150.1:n.*189C>A
ENST00000649242.1:c.*431C>A	ENSP00000497943.1:n.*431C>A
ENST00000649274.1:c.765C>A	ENSP00000497032.1:n.765C>A
ENST00000649518.1:c.*431C>A	ENSP00000498169.1:n.*431C>A
ENST00000649543.1:c.*431C>A	ENSP00000496826.1:n.*431C>A
ENST00000649752.1:c.554C>A	ENSP00000497267.1:p.Ser185Tyr
ENST00000650076.1:c.211+24291C>A
ENST00000650471.1:c.*271C>A	ENSP00000498027.1:n.*271C>A
ENST00000650604.1:c.254C>A	ENSP00000497105.1:p.Ser85Tyr
ENST00000373568.6:c.554C>A	ENSP00000362669.2:p.Ser185Tyr
ENST00000373573.7:c.827C>A	ENSP00000362674.3:p.Ser276Tyr
ENST00000373583.5:c.164+107415C>A	ENSP00000362685.1:n.164+107415C>A
ENST00000373589.8:c.554C>A	ENSP00000362691.4:p.Ser185Tyr
ENST00000415409.5:c.749C>A	ENSP00000396424.1:p.Ser250Tyr
ENST00000436675.5:c.*82C>A	ENSP00000416489.1:n.*82C>A
NM_001166418.1:c.554C>A	NP_001159890.1:p.Ser185Tyr
NM_018486.2:c.827C>A	NP_060956.1:p.Ser276Tyr
NR_051952.1:n.1027C>A
XM_011530986.1:c.827C>A	XP_011529288.1:p.Ser276Tyr
XM_011530987.1:c.827C>A	XP_011529289.1:p.Ser276Tyr
XM_011530988.1:c.827C>A	XP_011529290.1:p.Ser276Tyr
XR_938402.1:n.913C>A
XM_011530986.3:c.827C>A	XP_011529288.3:p.Ser276Tyr
XM_017029640.2:c.749C>A	XP_016885129.2:p.Ser250Tyr
XM_017029641.2:c.749C>A	XP_016885130.2:p.Ser250Tyr
XM_017029642.1:c.668C>A	XP_016885131.1:p.Ser223Tyr
XM_017029643.2:c.641C>A	XP_016885132.1:p.Ser214Tyr
XM_017029644.2:c.590C>A	XP_016885133.1:p.Ser197Tyr
XM_017029645.2:c.641C>A	XP_016885134.1:p.Ser214Tyr
XM_017029646.1:c.440C>A	XP_016885135.1:p.Ser147Tyr
XM_024452405.1:c.242C>A	XP_024308173.1:p.Ser81Tyr
XR_001755711.2:n.913C>A
XR_002958779.1:n.913C>A
XR_002958780.1:n.913C>A
XR_002958781.1:n.913C>A
XR_002958782.1:n.889C>A
XR_002958783.1:n.889C>A
XR_938402.3:n.913C>A
NM_018486.3:c.827C>A MANE Select	NP_060956.1:p.Ser276Tyr
NM_001166418.2:c.554C>A	NP_001159890.1:p.Ser185Tyr
NR_051952.2:n.767C>A