Canonical Allele Identifier: CA10603691

Gene: HDAC8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464682G>A , CM000685.2:g.72464682G>A	GRCh38
NC_000023.10:g.71684532G>A , CM000685.1:g.71684532G>A	GRCh37
NC_000023.9:g.71601257G>A	NCBI36
NG_015851.1:g.113422C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.787C>T	ENSP00000362669.3:p.Gln263Ter
ENST00000373573.9:c.787C>T MANE Select	ENSP00000362674.3:p.Gln263Ter
ENST00000373583.6:c.709C>T	ENSP00000362685.2:p.Gln237Ter
ENST00000373589.9:c.514C>T	ENSP00000362691.4:p.Gln172Ter
ENST00000412342.6:c.*485C>T	ENSP00000400180.1:n.*485C>T
ENST00000415409.6:c.787C>T	ENSP00000396424.2:p.Gln263Ter
ENST00000436675.6:c.*42C>T	ENSP00000416489.1:n.*42C>T
ENST00000478743.2:n.873C>T
ENST00000647594.1:c.787C>T	ENSP00000496814.1:p.Gln263Ter
ENST00000647606.1:c.562C>T
ENST00000647613.1:c.*540C>T	ENSP00000497911.1:n.*540C>T
ENST00000647641.1:n.874C>T
ENST00000647654.1:c.514C>T	ENSP00000497568.1:p.Gln172Ter
ENST00000647718.1:n.842C>T
ENST00000647859.1:c.787C>T	ENSP00000497530.1:p.Gln263Ter
ENST00000647886.1:c.787C>T	ENSP00000497188.1:p.Gln263Ter
ENST00000647980.1:c.781C>T	ENSP00000498002.1:p.Gln261Ter
ENST00000648139.1:c.487C>T	ENSP00000496818.1:p.Gln163Ter
ENST00000648276.1:c.31C>T	ENSP00000497619.1:p.Gln11Ter
ENST00000648285.1:n.570C>T
ENST00000648298.1:c.787C>T	ENSP00000496866.1:p.Gln263Ter
ENST00000648452.1:c.787C>T	ENSP00000497268.1:p.Gln263Ter
ENST00000648459.1:c.184C>T	ENSP00000498072.1:p.Gln62Ter
ENST00000648504.1:c.724C>T	ENSP00000497668.1:p.Gln242Ter
ENST00000648711.1:c.412C>T	ENSP00000498040.1:p.Gln138Ter
ENST00000648731.1:c.893C>T
ENST00000648834.1:c.787C>T	ENSP00000497764.1:p.Gln263Ter
ENST00000648850.1:c.422C>T
ENST00000648855.1:n.711C>T
ENST00000648870.1:c.787C>T	ENSP00000497599.1:p.Gln263Ter
ENST00000648922.1:c.787C>T	ENSP00000497072.1:p.Gln263Ter
ENST00000648939.1:c.787C>T	ENSP00000497442.1:p.Gln263Ter
ENST00000649097.1:c.787C>T	ENSP00000497551.1:p.Gln263Ter
ENST00000649116.1:c.*344C>T	ENSP00000497925.1:n.*344C>T
ENST00000649181.1:c.*149C>T	ENSP00000498150.1:n.*149C>T
ENST00000649242.1:c.*391C>T	ENSP00000497943.1:n.*391C>T
ENST00000649274.1:c.725C>T	ENSP00000497032.1:n.725C>T
ENST00000649518.1:c.*391C>T	ENSP00000498169.1:n.*391C>T
ENST00000649543.1:c.*391C>T	ENSP00000496826.1:n.*391C>T
ENST00000649752.1:c.514C>T	ENSP00000497267.1:p.Gln172Ter
ENST00000650076.1:c.211+24251C>T
ENST00000650471.1:c.*231C>T	ENSP00000498027.1:n.*231C>T
ENST00000650604.1:c.214C>T	ENSP00000497105.1:p.Gln72Ter
ENST00000373568.6:c.514C>T	ENSP00000362669.2:p.Gln172Ter
ENST00000373573.7:c.787C>T	ENSP00000362674.3:p.Gln263Ter
ENST00000373583.5:c.164+107375C>T	ENSP00000362685.1:n.164+107375C>T
ENST00000373589.8:c.514C>T	ENSP00000362691.4:p.Gln172Ter
ENST00000412342.5:c.*485C>T	ENSP00000400180.1:n.*485C>T
ENST00000415409.5:c.709C>T	ENSP00000396424.1:p.Gln237Ter
ENST00000436675.5:c.*42C>T	ENSP00000416489.1:n.*42C>T
NM_001166418.1:c.514C>T	NP_001159890.1:p.Gln172Ter
NM_018486.2:c.787C>T	NP_060956.1:p.Gln263Ter
NR_051952.1:n.987C>T
XM_011530986.1:c.787C>T	XP_011529288.1:p.Gln263Ter
XM_011530987.1:c.787C>T	XP_011529289.1:p.Gln263Ter
XM_011530988.1:c.787C>T	XP_011529290.1:p.Gln263Ter
XR_938402.1:n.873C>T
XM_011530986.3:c.787C>T	XP_011529288.3:p.Gln263Ter
XM_017029640.2:c.709C>T	XP_016885129.2:p.Gln237Ter
XM_017029641.2:c.709C>T	XP_016885130.2:p.Gln237Ter
XM_017029642.1:c.628C>T	XP_016885131.1:p.Gln210Ter
XM_017029643.2:c.601C>T	XP_016885132.1:p.Gln201Ter
XM_017029644.2:c.550C>T	XP_016885133.1:p.Gln184Ter
XM_017029645.2:c.601C>T	XP_016885134.1:p.Gln201Ter
XM_017029646.1:c.400C>T	XP_016885135.1:p.Gln134Ter
XM_024452405.1:c.202C>T	XP_024308173.1:p.Gln68Ter
XR_001755711.2:n.873C>T
XR_002958779.1:n.873C>T
XR_002958780.1:n.873C>T
XR_002958781.1:n.873C>T
XR_002958782.1:n.849C>T
XR_002958783.1:n.849C>T
XR_938402.3:n.873C>T
NM_018486.3:c.787C>T MANE Select	NP_060956.1:p.Gln263Ter
NM_001166418.2:c.514C>T	NP_001159890.1:p.Gln172Ter
NR_051952.2:n.727C>T