Canonical Allele Identifier: CA413642678

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684412C>G (hg19) ; chrX:g.72464562C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464562C>G , CM000685.2:g.72464562C>G	GRCh38
NC_000023.10:g.71684412C>G , CM000685.1:g.71684412C>G	GRCh37
NC_000023.9:g.71601137C>G	NCBI36
NG_015851.1:g.113542G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.907G>C	ENSP00000362669.3:p.Gly303Arg
ENST00000373573.9:c.907G>C MANE Select	ENSP00000362674.3:p.Gly303Arg
ENST00000373583.6:c.829G>C	ENSP00000362685.2:p.Gly277Arg
ENST00000373589.9:c.634G>C	ENSP00000362691.4:p.Gly212Arg
ENST00000415409.6:c.907G>C	ENSP00000396424.2:p.Gly303Arg
ENST00000436675.6:c.*162G>C	ENSP00000416489.1:n.*162G>C
ENST00000470998.2:c.3G>C
ENST00000478743.2:n.993G>C
ENST00000647594.1:c.907G>C	ENSP00000496814.1:p.Gly303Arg
ENST00000647606.1:c.682G>C
ENST00000647613.1:c.*660G>C	ENSP00000497911.1:n.*660G>C
ENST00000647641.1:n.994G>C
ENST00000647654.1:c.634G>C	ENSP00000497568.1:p.Gly212Arg
ENST00000647718.1:n.962G>C
ENST00000647859.1:c.907G>C	ENSP00000497530.1:p.Gly303Arg
ENST00000647886.1:c.907G>C	ENSP00000497188.1:p.Gly303Arg
ENST00000647980.1:c.901G>C	ENSP00000498002.1:p.Gly301Arg
ENST00000648139.1:c.607G>C	ENSP00000496818.1:p.Gly203Arg
ENST00000648276.1:c.151G>C	ENSP00000497619.1:p.Gly51Arg
ENST00000648285.1:n.690G>C
ENST00000648298.1:c.907G>C	ENSP00000496866.1:p.Gly303Arg
ENST00000648452.1:c.907G>C	ENSP00000497268.1:p.Gly303Arg
ENST00000648459.1:c.304G>C	ENSP00000498072.1:p.Gly102Arg
ENST00000648504.1:c.844G>C	ENSP00000497668.1:p.Gly282Arg
ENST00000648711.1:c.532G>C	ENSP00000498040.1:p.Gly178Arg
ENST00000648731.1:c.1013G>C
ENST00000648834.1:c.907G>C	ENSP00000497764.1:p.Gly303Arg
ENST00000648850.1:c.542G>C
ENST00000648855.1:n.831G>C
ENST00000648870.1:c.907G>C	ENSP00000497599.1:p.Gly303Arg
ENST00000648922.1:c.907G>C	ENSP00000497072.1:p.Gly303Arg
ENST00000648939.1:c.907G>C	ENSP00000497442.1:p.Gly303Arg
ENST00000649097.1:c.907G>C	ENSP00000497551.1:p.Gly303Arg
ENST00000649116.1:c.*464G>C	ENSP00000497925.1:n.*464G>C
ENST00000649181.1:c.*269G>C	ENSP00000498150.1:n.*269G>C
ENST00000649242.1:c.*511G>C	ENSP00000497943.1:n.*511G>C
ENST00000649274.1:c.845G>C	ENSP00000497032.1:n.845G>C
ENST00000649518.1:c.*511G>C	ENSP00000498169.1:n.*511G>C
ENST00000649543.1:c.*511G>C	ENSP00000496826.1:n.*511G>C
ENST00000649752.1:c.634G>C	ENSP00000497267.1:p.Gly212Arg
ENST00000650076.1:c.211+24371G>C
ENST00000650471.1:c.*351G>C	ENSP00000498027.1:n.*351G>C
ENST00000650604.1:c.334G>C	ENSP00000497105.1:p.Gly112Arg
ENST00000373568.6:c.634G>C	ENSP00000362669.2:p.Gly212Arg
ENST00000373573.7:c.907G>C	ENSP00000362674.3:p.Gly303Arg
ENST00000373583.5:c.164+107495G>C	ENSP00000362685.1:n.164+107495G>C
ENST00000373589.8:c.634G>C	ENSP00000362691.4:p.Gly212Arg
ENST00000415409.5:c.829G>C	ENSP00000396424.1:p.Gly277Arg
ENST00000436675.5:c.*162G>C	ENSP00000416489.1:n.*162G>C
NM_001166418.1:c.634G>C	NP_001159890.1:p.Gly212Arg
NM_018486.2:c.907G>C	NP_060956.1:p.Gly303Arg
NR_051952.1:n.1107G>C
XM_011530986.1:c.907G>C	XP_011529288.1:p.Gly303Arg
XM_011530987.1:c.907G>C	XP_011529289.1:p.Gly303Arg
XM_011530988.1:c.907G>C	XP_011529290.1:p.Gly303Arg
XR_938402.1:n.993G>C
XM_011530986.3:c.907G>C	XP_011529288.3:p.Gly303Arg
XM_017029640.2:c.829G>C	XP_016885129.2:p.Gly277Arg
XM_017029641.2:c.829G>C	XP_016885130.2:p.Gly277Arg
XM_017029642.1:c.748G>C	XP_016885131.1:p.Gly250Arg
XM_017029643.2:c.721G>C	XP_016885132.1:p.Gly241Arg
XM_017029644.2:c.670G>C	XP_016885133.1:p.Gly224Arg
XM_017029645.2:c.721G>C	XP_016885134.1:p.Gly241Arg
XM_017029646.1:c.520G>C	XP_016885135.1:p.Gly174Arg
XM_024452405.1:c.322G>C	XP_024308173.1:p.Gly108Arg
XR_001755711.2:n.993G>C
XR_002958779.1:n.993G>C
XR_002958780.1:n.993G>C
XR_002958781.1:n.993G>C
XR_002958782.1:n.969G>C
XR_002958783.1:n.969G>C
XR_938402.3:n.993G>C
NM_018486.3:c.907G>C MANE Select	NP_060956.1:p.Gly303Arg
NM_001166418.2:c.634G>C	NP_001159890.1:p.Gly212Arg
NR_051952.2:n.847G>C