Canonical Allele Identifier: CA413643446
Gene: HDAC8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72464732C>T , CM000685.2:g.72464732C>T GRCh38
NC_000023.10:g.71684582C>T , CM000685.1:g.71684582C>T GRCh37
NC_000023.9:g.71601307C>T NCBI36
NG_015851.1:g.113372G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373568.7:c.738-1G>A ENSP00000362669.3:n.738-1G>A
ENST00000373573.9:c.738-1G>A MANE Select ENSP00000362674.3:n.738-1G>A
ENST00000373583.6:c.660-1G>A ENSP00000362685.2:n.660-1G>A
ENST00000373589.9:c.465-1G>A ENSP00000362691.4:n.465-1G>A
ENST00000412342.6:c.*436-1G>A ENSP00000400180.1:n.*436-1G>A
ENST00000415409.6:c.738-1G>A ENSP00000396424.2:n.738-1G>A
ENST00000436675.6:c.551-1G>A ENSP00000416489.1:n.551-1G>A
ENST00000478743.2:n.824-1G>A
ENST00000647594.1:c.738-1G>A ENSP00000496814.1:n.738-1G>A
ENST00000647606.1:c.513-1G>A
ENST00000647613.1:c.*491-1G>A ENSP00000497911.1:n.*491-1G>A
ENST00000647641.1:n.825-1G>A
ENST00000647654.1:c.465-1G>A ENSP00000497568.1:n.465-1G>A
ENST00000647718.1:n.793-1G>A
ENST00000647859.1:c.738-1G>A ENSP00000497530.1:n.738-1G>A
ENST00000647886.1:c.738-1G>A ENSP00000497188.1:n.738-1G>A
ENST00000647980.1:c.732-1G>A ENSP00000498002.1:n.732-1G>A
ENST00000648139.1:c.438-1G>A ENSP00000496818.1:n.438-1G>A
ENST00000648285.1:n.521-1G>A
ENST00000648298.1:c.738-1G>A ENSP00000496866.1:n.738-1G>A
ENST00000648452.1:c.738-1G>A ENSP00000497268.1:n.738-1G>A
ENST00000648459.1:c.135-1G>A ENSP00000498072.1:n.135-1G>A
ENST00000648504.1:c.675-1G>A ENSP00000497668.1:n.675-1G>A
ENST00000648711.1:c.363-1G>A ENSP00000498040.1:n.363-1G>A
ENST00000648731.1:c.844-1G>A
ENST00000648834.1:c.738-1G>A ENSP00000497764.1:n.738-1G>A
ENST00000648850.1:c.373-1G>A
ENST00000648855.1:n.662-1G>A
ENST00000648870.1:c.738-1G>A ENSP00000497599.1:n.738-1G>A
ENST00000648922.1:c.738-1G>A ENSP00000497072.1:n.738-1G>A
ENST00000648939.1:c.738-1G>A ENSP00000497442.1:n.738-1G>A
ENST00000649097.1:c.738-1G>A ENSP00000497551.1:n.738-1G>A
ENST00000649116.1:c.*295-1G>A ENSP00000497925.1:n.*295-1G>A
ENST00000649181.1:c.*100-1G>A ENSP00000498150.1:n.*100-1G>A
ENST00000649242.1:c.*342-1G>A ENSP00000497943.1:n.*342-1G>A
ENST00000649274.1:c.676-1G>A ENSP00000497032.1:n.676-1G>A
ENST00000649518.1:c.*342-1G>A ENSP00000498169.1:n.*342-1G>A
ENST00000649543.1:c.*342-1G>A ENSP00000496826.1:n.*342-1G>A
ENST00000649752.1:c.465-1G>A ENSP00000497267.1:n.465-1G>A
ENST00000650076.1:c.211+24201G>A
ENST00000650471.1:c.*182-1G>A ENSP00000498027.1:n.*182-1G>A
ENST00000650604.1:c.165-1G>A ENSP00000497105.1:n.165-1G>A
ENST00000373568.6:c.465-1G>A ENSP00000362669.2:n.465-1G>A
ENST00000373573.7:c.738-1G>A ENSP00000362674.3:n.738-1G>A
ENST00000373583.5:c.164+107325G>A ENSP00000362685.1:n.164+107325G>A
ENST00000373589.8:c.465-1G>A ENSP00000362691.4:n.465-1G>A
ENST00000412342.5:c.*436-1G>A ENSP00000400180.1:n.*436-1G>A
ENST00000415409.5:c.660-1G>A ENSP00000396424.1:n.660-1G>A
ENST00000436675.5:c.551-1G>A ENSP00000416489.1:n.551-1G>A
NM_001166418.1:c.465-1G>A NP_001159890.1:n.465-1G>A
NM_018486.2:c.738-1G>A NP_060956.1:n.738-1G>A
NR_051952.1:n.938-1G>A
XM_011530986.1:c.738-1G>A XP_011529288.1:n.738-1G>A
XM_011530987.1:c.738-1G>A XP_011529289.1:n.738-1G>A
XM_011530988.1:c.738-1G>A XP_011529290.1:n.738-1G>A
XR_938402.1:n.824-1G>A
XM_011530986.3:c.738-1G>A XP_011529288.3:n.738-1G>A
XM_017029640.2:c.660-1G>A XP_016885129.2:n.660-1G>A
XM_017029641.2:c.660-1G>A XP_016885130.2:n.660-1G>A
XM_017029642.1:c.579-1G>A XP_016885131.1:n.579-1G>A
XM_017029643.2:c.552-1G>A XP_016885132.1:n.552-1G>A
XM_017029644.2:c.501-1G>A XP_016885133.1:n.501-1G>A
XM_017029645.2:c.552-1G>A XP_016885134.1:n.552-1G>A
XM_017029646.1:c.351-1G>A XP_016885135.1:n.351-1G>A
XM_024452405.1:c.153-1G>A XP_024308173.1:n.153-1G>A
XR_001755711.2:n.824-1G>A
XR_002958779.1:n.824-1G>A
XR_002958780.1:n.824-1G>A
XR_002958781.1:n.824-1G>A
XR_002958782.1:n.800-1G>A
XR_002958783.1:n.800-1G>A
XR_938402.3:n.824-1G>A
NM_018486.3:c.738-1G>A MANE Select NP_060956.1:n.738-1G>A
NM_001166418.2:c.465-1G>A NP_001159890.1:n.465-1G>A
NR_051952.2:n.678-1G>A
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