Canonical Allele Identifier: CA2694083666

Gene: HDAC8

Linked Data

• gnomAD v4: X-72464436-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464438del , CM000685.2:g.72464438del	GRCh38
NC_000023.10:g.71684288del , CM000685.1:g.71684288del	GRCh37
NC_000023.9:g.71601013del	NCBI36
NG_015851.1:g.113667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.910+122del	ENSP00000362669.3:n.910+122del
ENST00000373573.9:c.910+122del MANE Select	ENSP00000362674.3:n.910+122del
ENST00000373583.6:c.832+122del	ENSP00000362685.2:n.832+122del
ENST00000373589.9:c.637+122del	ENSP00000362691.4:n.637+122del
ENST00000415409.6:c.910+122del	ENSP00000396424.2:n.910+122del
ENST00000436675.6:c.*165+122del	ENSP00000416489.1:n.*165+122del
ENST00000470998.2:c.6+122del
ENST00000478743.2:n.996+122del
ENST00000647594.1:c.910+122del	ENSP00000496814.1:n.910+122del
ENST00000647606.1:c.685+122del
ENST00000647613.1:c.*663+122del	ENSP00000497911.1:n.*663+122del
ENST00000647641.1:n.997+122del
ENST00000647654.1:c.637+122del	ENSP00000497568.1:n.637+122del
ENST00000647718.1:n.1087del
ENST00000647859.1:c.910+122del	ENSP00000497530.1:n.910+122del
ENST00000647886.1:c.910+122del	ENSP00000497188.1:n.910+122del
ENST00000647980.1:c.904+122del	ENSP00000498002.1:n.904+122del
ENST00000648139.1:c.610+122del	ENSP00000496818.1:n.610+122del
ENST00000648276.1:c.154+122del	ENSP00000497619.1:n.154+122del
ENST00000648285.1:n.815del
ENST00000648298.1:c.910+122del	ENSP00000496866.1:n.910+122del
ENST00000648452.1:c.910+122del	ENSP00000497268.1:n.910+122del
ENST00000648459.1:c.307+122del	ENSP00000498072.1:n.307+122del
ENST00000648504.1:c.847+122del	ENSP00000497668.1:n.847+122del
ENST00000648711.1:c.535+122del	ENSP00000498040.1:n.535+122del
ENST00000648731.1:c.1016+122del
ENST00000648834.1:c.910+122del	ENSP00000497764.1:n.910+122del
ENST00000648850.1:c.545+122del
ENST00000648855.1:n.834+122del
ENST00000648870.1:c.910+122del	ENSP00000497599.1:n.910+122del
ENST00000648922.1:c.910+122del	ENSP00000497072.1:n.910+122del
ENST00000648939.1:c.910+122del	ENSP00000497442.1:n.910+122del
ENST00000649097.1:c.910+122del	ENSP00000497551.1:n.910+122del
ENST00000649116.1:c.*467+122del	ENSP00000497925.1:n.*467+122del
ENST00000649181.1:c.*272+122del	ENSP00000498150.1:n.*272+122del
ENST00000649242.1:c.*514+122del	ENSP00000497943.1:n.*514+122del
ENST00000649274.1:c.848+122del	ENSP00000497032.1:n.848+122del
ENST00000649518.1:c.*514+122del	ENSP00000498169.1:n.*514+122del
ENST00000649543.1:c.*514+122del	ENSP00000496826.1:n.*514+122del
ENST00000649752.1:c.637+122del	ENSP00000497267.1:n.637+122del
ENST00000650076.1:c.211+24496del
ENST00000650471.1:c.*354+122del	ENSP00000498027.1:n.*354+122del
ENST00000650604.1:c.337+122del	ENSP00000497105.1:n.337+122del
ENST00000373568.6:c.637+122del	ENSP00000362669.2:n.637+122del
ENST00000373573.7:c.910+122del	ENSP00000362674.3:n.910+122del
ENST00000373583.5:c.164+107620del	ENSP00000362685.1:n.164+107620del
ENST00000373589.8:c.637+122del	ENSP00000362691.4:n.637+122del
ENST00000415409.5:c.832+122del	ENSP00000396424.1:n.832+122del
ENST00000436675.5:c.*165+122del	ENSP00000416489.1:n.*165+122del
NM_001166418.1:c.637+122del	NP_001159890.1:n.637+122del
NM_018486.2:c.910+122del	NP_060956.1:n.910+122del
NR_051952.1:n.1110+122del
XM_011530986.1:c.910+122del	XP_011529288.1:n.910+122del
XM_011530987.1:c.910+122del	XP_011529289.1:n.910+122del
XM_011530988.1:c.910+122del	XP_011529290.1:n.910+122del
XR_938402.1:n.996+122del
XM_011530986.3:c.910+122del	XP_011529288.3:n.910+122del
XM_017029640.2:c.832+122del	XP_016885129.2:n.832+122del
XM_017029641.2:c.832+122del	XP_016885130.2:n.832+122del
XM_017029642.1:c.751+122del	XP_016885131.1:n.751+122del
XM_017029643.2:c.724+122del	XP_016885132.1:n.724+122del
XM_017029644.2:c.673+122del	XP_016885133.1:n.673+122del
XM_017029645.2:c.724+122del	XP_016885134.1:n.724+122del
XM_017029646.1:c.523+122del	XP_016885135.1:n.523+122del
XM_024452405.1:c.325+122del	XP_024308173.1:n.325+122del
XR_001755711.2:n.996+122del
XR_002958779.1:n.996+122del
XR_002958780.1:n.996+122del
XR_002958781.1:n.996+122del
XR_002958782.1:n.1094del
XR_002958783.1:n.972+122del
XR_938402.3:n.996+122del
NM_018486.3:c.910+122del MANE Select	NP_060956.1:n.910+122del
NM_001166418.2:c.637+122del	NP_001159890.1:n.637+122del
NR_051952.2:n.850+122del