Canonical Allele Identifier: CA10654773
Gene: HDAC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 369669
ClinVar RCV Id: RCV000408608
dbSNP Id: rs1057516037

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.72464626_72464630delinsAC , CM000685.2:g.72464626_72464630delinsAC GRCh38
NC_000023.10:g.71684476_71684480delinsAC , CM000685.1:g.71684476_71684480delinsAC GRCh37
NC_000023.9:g.71601201_71601205delinsAC NCBI36
NG_015851.1:g.113474_113478delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000373568.7:c.839_843delinsGT ENSP00000362669.3:p.Thr280_Pro281delinsSe...
ENST00000373573.9:c.839_843delinsGT MANE Select ENSP00000362674.3:p.Thr280_Pro281delinsSe...
ENST00000373583.6:c.761_765delinsGT ENSP00000362685.2:p.Thr254_Pro255delinsSe...
ENST00000373589.9:c.566_570delinsGT ENSP00000362691.4:p.Thr189_Pro190delinsSe...
ENST00000415409.6:c.839_843delinsGT ENSP00000396424.2:p.Thr280_Pro281delinsSe...
ENST00000436675.6:c.*94_*98delinsGT ENSP00000416489.1:n.*94_*98delinsGT
ENST00000478743.2:n.925_929delinsGT
ENST00000647594.1:c.839_843delinsGT ENSP00000496814.1:p.Thr280_Pro281delinsSe...
ENST00000647606.1:c.614_618delinsGT
ENST00000647613.1:c.*592_*596delinsGT ENSP00000497911.1:n.*592_*596delinsGT
ENST00000647641.1:n.926_930delinsGT
ENST00000647654.1:c.566_570delinsGT ENSP00000497568.1:p.Thr189_Pro190delinsSe...
ENST00000647718.1:n.894_898delinsGT
ENST00000647859.1:c.839_843delinsGT ENSP00000497530.1:p.Thr280_Pro281delinsSe...
ENST00000647886.1:c.839_843delinsGT ENSP00000497188.1:p.Thr280_Pro281delinsSe...
ENST00000647980.1:c.833_837delinsGT ENSP00000498002.1:p.Thr278_Pro279delinsSe...
ENST00000648139.1:c.539_543delinsGT ENSP00000496818.1:p.Thr180_Pro181delinsSe...
ENST00000648276.1:c.83_87delinsGT ENSP00000497619.1:p.Thr28_Pro29delinsSer
ENST00000648285.1:n.622_626delinsGT
ENST00000648298.1:c.839_843delinsGT ENSP00000496866.1:p.Thr280_Pro281delinsSe...
ENST00000648452.1:c.839_843delinsGT ENSP00000497268.1:p.Thr280_Pro281delinsSe...
ENST00000648459.1:c.236_240delinsGT ENSP00000498072.1:p.Thr79_Pro80delinsSer
ENST00000648504.1:c.776_780delinsGT ENSP00000497668.1:p.Thr259_Pro260delinsSe...
ENST00000648711.1:c.464_468delinsGT ENSP00000498040.1:p.Thr155_Pro156delinsSe...
ENST00000648731.1:c.945_949delinsGT
ENST00000648834.1:c.839_843delinsGT ENSP00000497764.1:p.Thr280_Pro281delinsSe...
ENST00000648850.1:c.474_478delinsGT
ENST00000648855.1:n.763_767delinsGT
ENST00000648870.1:c.839_843delinsGT ENSP00000497599.1:p.Thr280_Pro281delinsSe...
ENST00000648922.1:c.839_843delinsGT ENSP00000497072.1:p.Thr280_Pro281delinsSe...
ENST00000648939.1:c.839_843delinsGT ENSP00000497442.1:p.Thr280_Pro281delinsSe...
ENST00000649097.1:c.839_843delinsGT ENSP00000497551.1:p.Thr280_Pro281delinsSe...
ENST00000649116.1:c.*396_*400delinsGT ENSP00000497925.1:n.*396_*400delinsGT
ENST00000649181.1:c.*201_*205delinsGT ENSP00000498150.1:n.*201_*205delinsGT
ENST00000649242.1:c.*443_*447delinsGT ENSP00000497943.1:n.*443_*447delinsGT
ENST00000649274.1:c.777_781delinsGT ENSP00000497032.1:n.777_781delinsGT
ENST00000649518.1:c.*443_*447delinsGT ENSP00000498169.1:n.*443_*447delinsGT
ENST00000649543.1:c.*443_*447delinsGT ENSP00000496826.1:n.*443_*447delinsGT
ENST00000649752.1:c.566_570delinsGT ENSP00000497267.1:p.Thr189_Pro190delinsSe...
ENST00000650076.1:c.211+24303_211+24307delinsGT
ENST00000650471.1:c.*283_*287delinsGT ENSP00000498027.1:n.*283_*287delinsGT
ENST00000650604.1:c.266_270delinsGT ENSP00000497105.1:p.Thr89_Pro90delinsSer
ENST00000373568.6:c.566_570delinsGT ENSP00000362669.2:p.Thr189_Pro190delinsSe...
ENST00000373573.7:c.839_843delinsGT ENSP00000362674.3:p.Thr280_Pro281delinsSe...
ENST00000373583.5:c.164+107427_164+107431delinsGT ENSP00000362685.1:n.164+107427_164+107431...
ENST00000373589.8:c.566_570delinsGT ENSP00000362691.4:p.Thr189_Pro190delinsSe...
ENST00000415409.5:c.761_765delinsGT ENSP00000396424.1:p.Thr254_Pro255delinsSe...
ENST00000436675.5:c.*94_*98delinsGT ENSP00000416489.1:n.*94_*98delinsGT
NM_001166418.1:c.566_570delinsGT NP_001159890.1:p.Thr189_Pro190delinsSer
NM_018486.2:c.839_843delinsGT NP_060956.1:p.Thr280_Pro281delinsSer
NR_051952.1:n.1039_1043delinsGT
XM_011530986.1:c.839_843delinsGT XP_011529288.1:p.Thr280_Pro281delinsSer
XM_011530987.1:c.839_843delinsGT XP_011529289.1:p.Thr280_Pro281delinsSer
XM_011530988.1:c.839_843delinsGT XP_011529290.1:p.Thr280_Pro281delinsSer
XR_938402.1:n.925_929delinsGT
XM_011530986.3:c.839_843delinsGT XP_011529288.3:p.Thr280_Pro281delinsSer
XM_017029640.2:c.761_765delinsGT XP_016885129.2:p.Thr254_Pro255delinsSer
XM_017029641.2:c.761_765delinsGT XP_016885130.2:p.Thr254_Pro255delinsSer
XM_017029642.1:c.680_684delinsGT XP_016885131.1:p.Thr227_Pro228delinsSer
XM_017029643.2:c.653_657delinsGT XP_016885132.1:p.Thr218_Pro219delinsSer
XM_017029644.2:c.602_606delinsGT XP_016885133.1:p.Thr201_Pro202delinsSer
XM_017029645.2:c.653_657delinsGT XP_016885134.1:p.Thr218_Pro219delinsSer
XM_017029646.1:c.452_456delinsGT XP_016885135.1:p.Thr151_Pro152delinsSer
XM_024452405.1:c.254_258delinsGT XP_024308173.1:p.Thr85_Pro86delinsSer
XR_001755711.2:n.925_929delinsGT
XR_002958779.1:n.925_929delinsGT
XR_002958780.1:n.925_929delinsGT
XR_002958781.1:n.925_929delinsGT
XR_002958782.1:n.901_905delinsGT
XR_002958783.1:n.901_905delinsGT
XR_938402.3:n.925_929delinsGT
NM_018486.3:c.839_843delinsGT MANE Select NP_060956.1:p.Thr280_Pro281delinsSer
NM_001166418.2:c.566_570delinsGT NP_001159890.1:p.Thr189_Pro190delinsSer
NR_051952.2:n.779_783delinsGT