Canonical Allele Identifier: CA516779375

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684476T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464626T>G , CM000685.2:g.72464626T>G	GRCh38
NC_000023.10:g.71684476T>G , CM000685.1:g.71684476T>G	GRCh37
NC_000023.9:g.71601201T>G	NCBI36
NG_015851.1:g.113478A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.843A>C	ENSP00000362669.3:p.Pro281=
ENST00000373573.9:c.843A>C MANE Select	ENSP00000362674.3:p.Pro281=
ENST00000373583.6:c.765A>C	ENSP00000362685.2:p.Pro255=
ENST00000373589.9:c.570A>C	ENSP00000362691.4:p.Pro190=
ENST00000415409.6:c.843A>C	ENSP00000396424.2:p.Pro281=
ENST00000436675.6:c.*98A>C	ENSP00000416489.1:n.*98A>C
ENST00000478743.2:n.929A>C
ENST00000647594.1:c.843A>C	ENSP00000496814.1:p.Pro281=
ENST00000647606.1:c.618A>C
ENST00000647613.1:c.*596A>C	ENSP00000497911.1:n.*596A>C
ENST00000647641.1:n.930A>C
ENST00000647654.1:c.570A>C	ENSP00000497568.1:p.Pro190=
ENST00000647718.1:n.898A>C
ENST00000647859.1:c.843A>C	ENSP00000497530.1:p.Pro281=
ENST00000647886.1:c.843A>C	ENSP00000497188.1:p.Pro281=
ENST00000647980.1:c.837A>C	ENSP00000498002.1:p.Pro279=
ENST00000648139.1:c.543A>C	ENSP00000496818.1:p.Pro181=
ENST00000648276.1:c.87A>C	ENSP00000497619.1:p.Pro29=
ENST00000648285.1:n.626A>C
ENST00000648298.1:c.843A>C	ENSP00000496866.1:p.Pro281=
ENST00000648452.1:c.843A>C	ENSP00000497268.1:p.Pro281=
ENST00000648459.1:c.240A>C	ENSP00000498072.1:p.Pro80=
ENST00000648504.1:c.780A>C	ENSP00000497668.1:p.Pro260=
ENST00000648711.1:c.468A>C	ENSP00000498040.1:p.Pro156=
ENST00000648731.1:c.949A>C
ENST00000648834.1:c.843A>C	ENSP00000497764.1:p.Pro281=
ENST00000648850.1:c.478A>C
ENST00000648855.1:n.767A>C
ENST00000648870.1:c.843A>C	ENSP00000497599.1:p.Pro281=
ENST00000648922.1:c.843A>C	ENSP00000497072.1:p.Pro281=
ENST00000648939.1:c.843A>C	ENSP00000497442.1:p.Pro281=
ENST00000649097.1:c.843A>C	ENSP00000497551.1:p.Pro281=
ENST00000649116.1:c.*400A>C	ENSP00000497925.1:n.*400A>C
ENST00000649181.1:c.*205A>C	ENSP00000498150.1:n.*205A>C
ENST00000649242.1:c.*447A>C	ENSP00000497943.1:n.*447A>C
ENST00000649274.1:c.781A>C	ENSP00000497032.1:n.781A>C
ENST00000649518.1:c.*447A>C	ENSP00000498169.1:n.*447A>C
ENST00000649543.1:c.*447A>C	ENSP00000496826.1:n.*447A>C
ENST00000649752.1:c.570A>C	ENSP00000497267.1:p.Pro190=
ENST00000650076.1:c.211+24307A>C
ENST00000650471.1:c.*287A>C	ENSP00000498027.1:n.*287A>C
ENST00000650604.1:c.270A>C	ENSP00000497105.1:p.Pro90=
ENST00000373568.6:c.570A>C	ENSP00000362669.2:p.Pro190=
ENST00000373573.7:c.843A>C	ENSP00000362674.3:p.Pro281=
ENST00000373583.5:c.164+107431A>C	ENSP00000362685.1:n.164+107431A>C
ENST00000373589.8:c.570A>C	ENSP00000362691.4:p.Pro190=
ENST00000415409.5:c.765A>C	ENSP00000396424.1:p.Pro255=
ENST00000436675.5:c.*98A>C	ENSP00000416489.1:n.*98A>C
NM_001166418.1:c.570A>C	NP_001159890.1:p.Pro190=
NM_018486.2:c.843A>C	NP_060956.1:p.Pro281=
NR_051952.1:n.1043A>C
XM_011530986.1:c.843A>C	XP_011529288.1:p.Pro281=
XM_011530987.1:c.843A>C	XP_011529289.1:p.Pro281=
XM_011530988.1:c.843A>C	XP_011529290.1:p.Pro281=
XR_938402.1:n.929A>C
XM_011530986.3:c.843A>C	XP_011529288.3:p.Pro281=
XM_017029640.2:c.765A>C	XP_016885129.2:p.Pro255=
XM_017029641.2:c.765A>C	XP_016885130.2:p.Pro255=
XM_017029642.1:c.684A>C	XP_016885131.1:p.Pro228=
XM_017029643.2:c.657A>C	XP_016885132.1:p.Pro219=
XM_017029644.2:c.606A>C	XP_016885133.1:p.Pro202=
XM_017029645.2:c.657A>C	XP_016885134.1:p.Pro219=
XM_017029646.1:c.456A>C	XP_016885135.1:p.Pro152=
XM_024452405.1:c.258A>C	XP_024308173.1:p.Pro86=
XR_001755711.2:n.929A>C
XR_002958779.1:n.929A>C
XR_002958780.1:n.929A>C
XR_002958781.1:n.929A>C
XR_002958782.1:n.905A>C
XR_002958783.1:n.905A>C
XR_938402.3:n.929A>C
NM_018486.3:c.843A>C MANE Select	NP_060956.1:p.Pro281=
NM_001166418.2:c.570A>C	NP_001159890.1:p.Pro190=
NR_051952.2:n.783A>C