Canonical Allele Identifier: CA413643008

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684482C>A (hg19) ; chrX:g.72464632C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464632C>A , CM000685.2:g.72464632C>A	GRCh38
NC_000023.10:g.71684482C>A , CM000685.1:g.71684482C>A	GRCh37
NC_000023.9:g.71601207C>A	NCBI36
NG_015851.1:g.113472G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.837G>T	ENSP00000362669.3:p.Met279Ile
ENST00000373573.9:c.837G>T MANE Select	ENSP00000362674.3:p.Met279Ile
ENST00000373583.6:c.759G>T	ENSP00000362685.2:p.Met253Ile
ENST00000373589.9:c.564G>T	ENSP00000362691.4:p.Met188Ile
ENST00000415409.6:c.837G>T	ENSP00000396424.2:p.Met279Ile
ENST00000436675.6:c.*92G>T	ENSP00000416489.1:n.*92G>T
ENST00000478743.2:n.923G>T
ENST00000647594.1:c.837G>T	ENSP00000496814.1:p.Met279Ile
ENST00000647606.1:c.612G>T
ENST00000647613.1:c.*590G>T	ENSP00000497911.1:n.*590G>T
ENST00000647641.1:n.924G>T
ENST00000647654.1:c.564G>T	ENSP00000497568.1:p.Met188Ile
ENST00000647718.1:n.892G>T
ENST00000647859.1:c.837G>T	ENSP00000497530.1:p.Met279Ile
ENST00000647886.1:c.837G>T	ENSP00000497188.1:p.Met279Ile
ENST00000647980.1:c.831G>T	ENSP00000498002.1:p.Met277Ile
ENST00000648139.1:c.537G>T	ENSP00000496818.1:p.Met179Ile
ENST00000648276.1:c.81G>T	ENSP00000497619.1:p.Met27Ile
ENST00000648285.1:n.620G>T
ENST00000648298.1:c.837G>T	ENSP00000496866.1:p.Met279Ile
ENST00000648452.1:c.837G>T	ENSP00000497268.1:p.Met279Ile
ENST00000648459.1:c.234G>T	ENSP00000498072.1:p.Met78Ile
ENST00000648504.1:c.774G>T	ENSP00000497668.1:p.Met258Ile
ENST00000648711.1:c.462G>T	ENSP00000498040.1:p.Met154Ile
ENST00000648731.1:c.943G>T
ENST00000648834.1:c.837G>T	ENSP00000497764.1:p.Met279Ile
ENST00000648850.1:c.472G>T
ENST00000648855.1:n.761G>T
ENST00000648870.1:c.837G>T	ENSP00000497599.1:p.Met279Ile
ENST00000648922.1:c.837G>T	ENSP00000497072.1:p.Met279Ile
ENST00000648939.1:c.837G>T	ENSP00000497442.1:p.Met279Ile
ENST00000649097.1:c.837G>T	ENSP00000497551.1:p.Met279Ile
ENST00000649116.1:c.*394G>T	ENSP00000497925.1:n.*394G>T
ENST00000649181.1:c.*199G>T	ENSP00000498150.1:n.*199G>T
ENST00000649242.1:c.*441G>T	ENSP00000497943.1:n.*441G>T
ENST00000649274.1:c.775G>T	ENSP00000497032.1:n.775G>T
ENST00000649518.1:c.*441G>T	ENSP00000498169.1:n.*441G>T
ENST00000649543.1:c.*441G>T	ENSP00000496826.1:n.*441G>T
ENST00000649752.1:c.564G>T	ENSP00000497267.1:p.Met188Ile
ENST00000650076.1:c.211+24301G>T
ENST00000650471.1:c.*281G>T	ENSP00000498027.1:n.*281G>T
ENST00000650604.1:c.264G>T	ENSP00000497105.1:p.Met88Ile
ENST00000373568.6:c.564G>T	ENSP00000362669.2:p.Met188Ile
ENST00000373573.7:c.837G>T	ENSP00000362674.3:p.Met279Ile
ENST00000373583.5:c.164+107425G>T	ENSP00000362685.1:n.164+107425G>T
ENST00000373589.8:c.564G>T	ENSP00000362691.4:p.Met188Ile
ENST00000415409.5:c.759G>T	ENSP00000396424.1:p.Met253Ile
ENST00000436675.5:c.*92G>T	ENSP00000416489.1:n.*92G>T
NM_001166418.1:c.564G>T	NP_001159890.1:p.Met188Ile
NM_018486.2:c.837G>T	NP_060956.1:p.Met279Ile
NR_051952.1:n.1037G>T
XM_011530986.1:c.837G>T	XP_011529288.1:p.Met279Ile
XM_011530987.1:c.837G>T	XP_011529289.1:p.Met279Ile
XM_011530988.1:c.837G>T	XP_011529290.1:p.Met279Ile
XR_938402.1:n.923G>T
XM_011530986.3:c.837G>T	XP_011529288.3:p.Met279Ile
XM_017029640.2:c.759G>T	XP_016885129.2:p.Met253Ile
XM_017029641.2:c.759G>T	XP_016885130.2:p.Met253Ile
XM_017029642.1:c.678G>T	XP_016885131.1:p.Met226Ile
XM_017029643.2:c.651G>T	XP_016885132.1:p.Met217Ile
XM_017029644.2:c.600G>T	XP_016885133.1:p.Met200Ile
XM_017029645.2:c.651G>T	XP_016885134.1:p.Met217Ile
XM_017029646.1:c.450G>T	XP_016885135.1:p.Met150Ile
XM_024452405.1:c.252G>T	XP_024308173.1:p.Met84Ile
XR_001755711.2:n.923G>T
XR_002958779.1:n.923G>T
XR_002958780.1:n.923G>T
XR_002958781.1:n.923G>T
XR_002958782.1:n.899G>T
XR_002958783.1:n.899G>T
XR_938402.3:n.923G>T
NM_018486.3:c.837G>T MANE Select	NP_060956.1:p.Met279Ile
NM_001166418.2:c.564G>T	NP_001159890.1:p.Met188Ile
NR_051952.2:n.777G>T