Canonical Allele Identifier: CA516779337

Gene: HDAC8

Linked Data

• dbSNP Id: rs2047961320
• MyVariant Identifiers: chrX:g.71684422G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464572G>A , CM000685.2:g.72464572G>A	GRCh38
NC_000023.10:g.71684422G>A , CM000685.1:g.71684422G>A	GRCh37
NC_000023.9:g.71601147G>A	NCBI36
NG_015851.1:g.113532C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.897C>T	ENSP00000362669.3:p.Leu299=
ENST00000373573.9:c.897C>T MANE Select	ENSP00000362674.3:p.Leu299=
ENST00000373583.6:c.819C>T	ENSP00000362685.2:p.Leu273=
ENST00000373589.9:c.624C>T	ENSP00000362691.4:p.Leu208=
ENST00000415409.6:c.897C>T	ENSP00000396424.2:p.Leu299=
ENST00000436675.6:c.*152C>T	ENSP00000416489.1:n.*152C>T
ENST00000478743.2:n.983C>T
ENST00000647594.1:c.897C>T	ENSP00000496814.1:p.Leu299=
ENST00000647606.1:c.672C>T
ENST00000647613.1:c.*650C>T	ENSP00000497911.1:n.*650C>T
ENST00000647641.1:n.984C>T
ENST00000647654.1:c.624C>T	ENSP00000497568.1:p.Leu208=
ENST00000647718.1:n.952C>T
ENST00000647859.1:c.897C>T	ENSP00000497530.1:p.Leu299=
ENST00000647886.1:c.897C>T	ENSP00000497188.1:p.Leu299=
ENST00000647980.1:c.891C>T	ENSP00000498002.1:p.Leu297=
ENST00000648139.1:c.597C>T	ENSP00000496818.1:p.Leu199=
ENST00000648276.1:c.141C>T	ENSP00000497619.1:p.Leu47=
ENST00000648285.1:n.680C>T
ENST00000648298.1:c.897C>T	ENSP00000496866.1:p.Leu299=
ENST00000648452.1:c.897C>T	ENSP00000497268.1:p.Leu299=
ENST00000648459.1:c.294C>T	ENSP00000498072.1:p.Leu98=
ENST00000648504.1:c.834C>T	ENSP00000497668.1:p.Leu278=
ENST00000648711.1:c.522C>T	ENSP00000498040.1:p.Leu174=
ENST00000648731.1:c.1003C>T
ENST00000648834.1:c.897C>T	ENSP00000497764.1:p.Leu299=
ENST00000648850.1:c.532C>T
ENST00000648855.1:n.821C>T
ENST00000648870.1:c.897C>T	ENSP00000497599.1:p.Leu299=
ENST00000648922.1:c.897C>T	ENSP00000497072.1:p.Leu299=
ENST00000648939.1:c.897C>T	ENSP00000497442.1:p.Leu299=
ENST00000649097.1:c.897C>T	ENSP00000497551.1:p.Leu299=
ENST00000649116.1:c.*454C>T	ENSP00000497925.1:n.*454C>T
ENST00000649181.1:c.*259C>T	ENSP00000498150.1:n.*259C>T
ENST00000649242.1:c.*501C>T	ENSP00000497943.1:n.*501C>T
ENST00000649274.1:c.835C>T	ENSP00000497032.1:n.835C>T
ENST00000649518.1:c.*501C>T	ENSP00000498169.1:n.*501C>T
ENST00000649543.1:c.*501C>T	ENSP00000496826.1:n.*501C>T
ENST00000649752.1:c.624C>T	ENSP00000497267.1:p.Leu208=
ENST00000650076.1:c.211+24361C>T
ENST00000650471.1:c.*341C>T	ENSP00000498027.1:n.*341C>T
ENST00000650604.1:c.324C>T	ENSP00000497105.1:p.Leu108=
ENST00000373568.6:c.624C>T	ENSP00000362669.2:p.Leu208=
ENST00000373573.7:c.897C>T	ENSP00000362674.3:p.Leu299=
ENST00000373583.5:c.164+107485C>T	ENSP00000362685.1:n.164+107485C>T
ENST00000373589.8:c.624C>T	ENSP00000362691.4:p.Leu208=
ENST00000415409.5:c.819C>T	ENSP00000396424.1:p.Leu273=
ENST00000436675.5:c.*152C>T	ENSP00000416489.1:n.*152C>T
NM_001166418.1:c.624C>T	NP_001159890.1:p.Leu208=
NM_018486.2:c.897C>T	NP_060956.1:p.Leu299=
NR_051952.1:n.1097C>T
XM_011530986.1:c.897C>T	XP_011529288.1:p.Leu299=
XM_011530987.1:c.897C>T	XP_011529289.1:p.Leu299=
XM_011530988.1:c.897C>T	XP_011529290.1:p.Leu299=
XR_938402.1:n.983C>T
XM_011530986.3:c.897C>T	XP_011529288.3:p.Leu299=
XM_017029640.2:c.819C>T	XP_016885129.2:p.Leu273=
XM_017029641.2:c.819C>T	XP_016885130.2:p.Leu273=
XM_017029642.1:c.738C>T	XP_016885131.1:p.Leu246=
XM_017029643.2:c.711C>T	XP_016885132.1:p.Leu237=
XM_017029644.2:c.660C>T	XP_016885133.1:p.Leu220=
XM_017029645.2:c.711C>T	XP_016885134.1:p.Leu237=
XM_017029646.1:c.510C>T	XP_016885135.1:p.Leu170=
XM_024452405.1:c.312C>T	XP_024308173.1:p.Leu104=
XR_001755711.2:n.983C>T
XR_002958779.1:n.983C>T
XR_002958780.1:n.983C>T
XR_002958781.1:n.983C>T
XR_002958782.1:n.959C>T
XR_002958783.1:n.959C>T
XR_938402.3:n.983C>T
NM_018486.3:c.897C>T MANE Select	NP_060956.1:p.Leu299=
NM_001166418.2:c.624C>T	NP_001159890.1:p.Leu208=
NR_051952.2:n.837C>T