Canonical Allele Identifier: CA10450206

Gene: HDAC8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72489001C>A , CM000685.2:g.72489001C>A	GRCh38
NC_000023.10:g.71708851C>A , CM000685.1:g.71708851C>A	GRCh37
NC_000023.9:g.71625576C>A	NCBI36
NG_015851.1:g.89103G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373560.7:c.438-14272G>T	ENSP00000362661.2:n.438-14272G>T
ENST00000373568.7:c.669G>T	ENSP00000362669.3:p.Arg223=
ENST00000373571.6:c.669G>T	ENSP00000362672.1:p.Arg223=
ENST00000373573.9:c.669G>T MANE Select	ENSP00000362674.3:p.Arg223=
ENST00000373583.6:c.591G>T	ENSP00000362685.2:p.Arg197=
ENST00000373589.9:c.396G>T	ENSP00000362691.4:p.Arg132=
ENST00000412342.6:c.*367G>T	ENSP00000400180.1:n.*367G>T
ENST00000415409.6:c.669G>T	ENSP00000396424.2:p.Arg223=
ENST00000436675.6:c.550+6155G>T	ENSP00000416489.1:n.550+6155G>T
ENST00000439122.7:c.669G>T	ENSP00000414486.2:p.Arg223=
ENST00000478743.2:n.755G>T
ENST00000647594.1:c.669G>T	ENSP00000496814.1:p.Arg223=
ENST00000647606.1:c.444G>T
ENST00000647613.1:c.*422G>T	ENSP00000497911.1:n.*422G>T
ENST00000647641.1:n.756G>T
ENST00000647654.1:c.396G>T	ENSP00000497568.1:p.Arg132=
ENST00000647718.1:n.724G>T
ENST00000647859.1:c.669G>T	ENSP00000497530.1:p.Arg223=
ENST00000647886.1:c.669G>T	ENSP00000497188.1:p.Arg223=
ENST00000647974.1:c.413G>T
ENST00000647980.1:c.663G>T	ENSP00000498002.1:p.Arg221=
ENST00000648036.1:c.663G>T	ENSP00000496994.1:p.Arg221=
ENST00000648139.1:c.438-24270G>T	ENSP00000496818.1:n.438-24270G>T
ENST00000648285.1:n.452G>T
ENST00000648298.1:c.669G>T	ENSP00000496866.1:p.Arg223=
ENST00000648452.1:c.669G>T	ENSP00000497268.1:p.Arg223=
ENST00000648459.1:c.135-24270G>T	ENSP00000498072.1:n.135-24270G>T
ENST00000648504.1:c.606G>T	ENSP00000497668.1:p.Arg202=
ENST00000648577.1:c.*273G>T	ENSP00000497552.1:n.*273G>T
ENST00000648711.1:c.294G>T	ENSP00000498040.1:p.Arg98=
ENST00000648731.1:c.775G>T
ENST00000648834.1:c.669G>T	ENSP00000497764.1:p.Arg223=
ENST00000648850.1:c.304G>T
ENST00000648855.1:n.593G>T
ENST00000648870.1:c.669G>T	ENSP00000497599.1:p.Arg223=
ENST00000648922.1:c.669G>T	ENSP00000497072.1:p.Arg223=
ENST00000648939.1:c.669G>T	ENSP00000497442.1:p.Arg223=
ENST00000648962.1:c.550+6155G>T	ENSP00000497516.1:n.550+6155G>T
ENST00000649097.1:c.669G>T	ENSP00000497551.1:p.Arg223=
ENST00000649116.1:c.*226G>T	ENSP00000497925.1:n.*226G>T
ENST00000649181.1:c.*31G>T	ENSP00000498150.1:n.*31G>T
ENST00000649242.1:c.*273G>T	ENSP00000497943.1:n.*273G>T
ENST00000649274.1:c.607G>T	ENSP00000497032.1:n.607G>T
ENST00000649518.1:c.*273G>T	ENSP00000498169.1:n.*273G>T
ENST00000649543.1:c.*273G>T	ENSP00000496826.1:n.*273G>T
ENST00000649752.1:c.396G>T	ENSP00000497267.1:p.Arg132=
ENST00000650076.1:c.143G>T
ENST00000650126.1:c.591G>T	ENSP00000498144.1:p.Arg197=
ENST00000650471.1:c.*113G>T	ENSP00000498027.1:n.*113G>T
ENST00000650604.1:c.165-24270G>T	ENSP00000497105.1:n.165-24270G>T
ENST00000373559.8:c.318G>T	ENSP00000362660.4:p.Arg106=
ENST00000373560.6:c.438-14272G>T	ENSP00000362661.2:n.438-14272G>T
ENST00000373568.6:c.396G>T	ENSP00000362669.2:p.Arg132=
ENST00000373571.5:c.669G>T	ENSP00000362672.1:p.Arg223=
ENST00000373573.7:c.669G>T	ENSP00000362674.3:p.Arg223=
ENST00000373583.5:c.164+83056G>T	ENSP00000362685.1:n.164+83056G>T
ENST00000373589.8:c.396G>T	ENSP00000362691.4:p.Arg132=
ENST00000412342.5:c.*367G>T	ENSP00000400180.1:n.*367G>T
ENST00000415409.5:c.591G>T	ENSP00000396424.1:p.Arg197=
ENST00000436675.5:c.550+6155G>T	ENSP00000416489.1:n.550+6155G>T
ENST00000439122.6:c.669G>T	ENSP00000414486.2:p.Arg223=
NM_001166418.1:c.396G>T	NP_001159890.1:p.Arg132=
NM_001166419.1:c.669G>T	NP_001159891.1:p.Arg223=
NM_001166448.1:c.318G>T	NP_001159920.1:p.Arg106=
NM_018486.2:c.669G>T	NP_060956.1:p.Arg223=
NR_051952.1:n.869G>T
XM_011530986.1:c.669G>T	XP_011529288.1:p.Arg223=
XM_011530987.1:c.669G>T	XP_011529289.1:p.Arg223=
XM_011530988.1:c.669G>T	XP_011529290.1:p.Arg223=
XR_938402.1:n.755G>T
XM_011530986.3:c.669G>T	XP_011529288.3:p.Arg223=
XM_017029640.2:c.591G>T	XP_016885129.2:p.Arg197=
XM_017029641.2:c.591G>T	XP_016885130.2:p.Arg197=
XM_017029642.1:c.510G>T	XP_016885131.1:p.Arg170=
XM_017029643.2:c.552-24270G>T	XP_016885132.1:n.552-24270G>T
XM_017029644.2:c.432G>T	XP_016885133.1:p.Arg144=
XM_017029645.2:c.552-24270G>T	XP_016885134.1:n.552-24270G>T
XM_017029646.1:c.282G>T	XP_016885135.1:p.Arg94=
XM_017029647.2:c.591G>T	XP_016885136.2:p.Arg197=
XM_024452405.1:c.84G>T	XP_024308173.1:p.Arg28=
XR_001755711.2:n.755G>T
XR_002958779.1:n.755G>T
XR_002958780.1:n.755G>T
XR_002958781.1:n.755G>T
XR_002958782.1:n.731G>T
XR_002958783.1:n.731G>T
XR_938402.3:n.755G>T
NM_018486.3:c.669G>T MANE Select	NP_060956.1:p.Arg223=
NM_001166418.2:c.396G>T	NP_001159890.1:p.Arg132=
NM_001166419.2:c.669G>T	NP_001159891.1:p.Arg223=
NM_001166448.2:c.318G>T	NP_001159920.1:p.Arg106=
NR_051952.2:n.609G>T