Canonical Allele Identifier: CA413643178

Gene: HDAC8

Linked Data

• gnomAD v4: X-72464672-G-A
• MyVariant Identifiers: chrX:g.71684522G>A (hg19) ; chrX:g.72464672G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464672G>A , CM000685.2:g.72464672G>A	GRCh38
NC_000023.10:g.71684522G>A , CM000685.1:g.71684522G>A	GRCh37
NC_000023.9:g.71601247G>A	NCBI36
NG_015851.1:g.113432C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.797C>T	ENSP00000362669.3:p.Ala266Val
ENST00000373573.9:c.797C>T MANE Select	ENSP00000362674.3:p.Ala266Val
ENST00000373583.6:c.719C>T	ENSP00000362685.2:p.Ala240Val
ENST00000373589.9:c.524C>T	ENSP00000362691.4:p.Ala175Val
ENST00000412342.6:c.*495C>T	ENSP00000400180.1:n.*495C>T
ENST00000415409.6:c.797C>T	ENSP00000396424.2:p.Ala266Val
ENST00000436675.6:c.*52C>T	ENSP00000416489.1:n.*52C>T
ENST00000478743.2:n.883C>T
ENST00000647594.1:c.797C>T	ENSP00000496814.1:p.Ala266Val
ENST00000647606.1:c.572C>T
ENST00000647613.1:c.*550C>T	ENSP00000497911.1:n.*550C>T
ENST00000647641.1:n.884C>T
ENST00000647654.1:c.524C>T	ENSP00000497568.1:p.Ala175Val
ENST00000647718.1:n.852C>T
ENST00000647859.1:c.797C>T	ENSP00000497530.1:p.Ala266Val
ENST00000647886.1:c.797C>T	ENSP00000497188.1:p.Ala266Val
ENST00000647980.1:c.791C>T	ENSP00000498002.1:p.Ala264Val
ENST00000648139.1:c.497C>T	ENSP00000496818.1:p.Ala166Val
ENST00000648276.1:c.41C>T	ENSP00000497619.1:p.Ala14Val
ENST00000648285.1:n.580C>T
ENST00000648298.1:c.797C>T	ENSP00000496866.1:p.Ala266Val
ENST00000648452.1:c.797C>T	ENSP00000497268.1:p.Ala266Val
ENST00000648459.1:c.194C>T	ENSP00000498072.1:p.Ala65Val
ENST00000648504.1:c.734C>T	ENSP00000497668.1:p.Ala245Val
ENST00000648711.1:c.422C>T	ENSP00000498040.1:p.Ala141Val
ENST00000648731.1:c.903C>T
ENST00000648834.1:c.797C>T	ENSP00000497764.1:p.Ala266Val
ENST00000648850.1:c.432C>T
ENST00000648855.1:n.721C>T
ENST00000648870.1:c.797C>T	ENSP00000497599.1:p.Ala266Val
ENST00000648922.1:c.797C>T	ENSP00000497072.1:p.Ala266Val
ENST00000648939.1:c.797C>T	ENSP00000497442.1:p.Ala266Val
ENST00000649097.1:c.797C>T	ENSP00000497551.1:p.Ala266Val
ENST00000649116.1:c.*354C>T	ENSP00000497925.1:n.*354C>T
ENST00000649181.1:c.*159C>T	ENSP00000498150.1:n.*159C>T
ENST00000649242.1:c.*401C>T	ENSP00000497943.1:n.*401C>T
ENST00000649274.1:c.735C>T	ENSP00000497032.1:n.735C>T
ENST00000649518.1:c.*401C>T	ENSP00000498169.1:n.*401C>T
ENST00000649543.1:c.*401C>T	ENSP00000496826.1:n.*401C>T
ENST00000649752.1:c.524C>T	ENSP00000497267.1:p.Ala175Val
ENST00000650076.1:c.211+24261C>T
ENST00000650471.1:c.*241C>T	ENSP00000498027.1:n.*241C>T
ENST00000650604.1:c.224C>T	ENSP00000497105.1:p.Ala75Val
ENST00000373568.6:c.524C>T	ENSP00000362669.2:p.Ala175Val
ENST00000373573.7:c.797C>T	ENSP00000362674.3:p.Ala266Val
ENST00000373583.5:c.164+107385C>T	ENSP00000362685.1:n.164+107385C>T
ENST00000373589.8:c.524C>T	ENSP00000362691.4:p.Ala175Val
ENST00000412342.5:c.*495C>T	ENSP00000400180.1:n.*495C>T
ENST00000415409.5:c.719C>T	ENSP00000396424.1:p.Ala240Val
ENST00000436675.5:c.*52C>T	ENSP00000416489.1:n.*52C>T
NM_001166418.1:c.524C>T	NP_001159890.1:p.Ala175Val
NM_018486.2:c.797C>T	NP_060956.1:p.Ala266Val
NR_051952.1:n.997C>T
XM_011530986.1:c.797C>T	XP_011529288.1:p.Ala266Val
XM_011530987.1:c.797C>T	XP_011529289.1:p.Ala266Val
XM_011530988.1:c.797C>T	XP_011529290.1:p.Ala266Val
XR_938402.1:n.883C>T
XM_011530986.3:c.797C>T	XP_011529288.3:p.Ala266Val
XM_017029640.2:c.719C>T	XP_016885129.2:p.Ala240Val
XM_017029641.2:c.719C>T	XP_016885130.2:p.Ala240Val
XM_017029642.1:c.638C>T	XP_016885131.1:p.Ala213Val
XM_017029643.2:c.611C>T	XP_016885132.1:p.Ala204Val
XM_017029644.2:c.560C>T	XP_016885133.1:p.Ala187Val
XM_017029645.2:c.611C>T	XP_016885134.1:p.Ala204Val
XM_017029646.1:c.410C>T	XP_016885135.1:p.Ala137Val
XM_024452405.1:c.212C>T	XP_024308173.1:p.Ala71Val
XR_001755711.2:n.883C>T
XR_002958779.1:n.883C>T
XR_002958780.1:n.883C>T
XR_002958781.1:n.883C>T
XR_002958782.1:n.859C>T
XR_002958783.1:n.859C>T
XR_938402.3:n.883C>T
NM_018486.3:c.797C>T MANE Select	NP_060956.1:p.Ala266Val
NM_001166418.2:c.524C>T	NP_001159890.1:p.Ala175Val
NR_051952.2:n.737C>T