Canonical Allele Identifier: CA413643014

Gene: HDAC8

Linked Data

• MyVariant Identifiers: chrX:g.71684483A>G (hg19) ; chrX:g.72464633A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72464633A>G , CM000685.2:g.72464633A>G	GRCh38
NC_000023.10:g.71684483A>G , CM000685.1:g.71684483A>G	GRCh37
NC_000023.9:g.71601208A>G	NCBI36
NG_015851.1:g.113471T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373568.7:c.836T>C	ENSP00000362669.3:p.Met279Thr
ENST00000373573.9:c.836T>C MANE Select	ENSP00000362674.3:p.Met279Thr
ENST00000373583.6:c.758T>C	ENSP00000362685.2:p.Met253Thr
ENST00000373589.9:c.563T>C	ENSP00000362691.4:p.Met188Thr
ENST00000415409.6:c.836T>C	ENSP00000396424.2:p.Met279Thr
ENST00000436675.6:c.*91T>C	ENSP00000416489.1:n.*91T>C
ENST00000478743.2:n.922T>C
ENST00000647594.1:c.836T>C	ENSP00000496814.1:p.Met279Thr
ENST00000647606.1:c.611T>C
ENST00000647613.1:c.*589T>C	ENSP00000497911.1:n.*589T>C
ENST00000647641.1:n.923T>C
ENST00000647654.1:c.563T>C	ENSP00000497568.1:p.Met188Thr
ENST00000647718.1:n.891T>C
ENST00000647859.1:c.836T>C	ENSP00000497530.1:p.Met279Thr
ENST00000647886.1:c.836T>C	ENSP00000497188.1:p.Met279Thr
ENST00000647980.1:c.830T>C	ENSP00000498002.1:p.Met277Thr
ENST00000648139.1:c.536T>C	ENSP00000496818.1:p.Met179Thr
ENST00000648276.1:c.80T>C	ENSP00000497619.1:p.Met27Thr
ENST00000648285.1:n.619T>C
ENST00000648298.1:c.836T>C	ENSP00000496866.1:p.Met279Thr
ENST00000648452.1:c.836T>C	ENSP00000497268.1:p.Met279Thr
ENST00000648459.1:c.233T>C	ENSP00000498072.1:p.Met78Thr
ENST00000648504.1:c.773T>C	ENSP00000497668.1:p.Met258Thr
ENST00000648711.1:c.461T>C	ENSP00000498040.1:p.Met154Thr
ENST00000648731.1:c.942T>C
ENST00000648834.1:c.836T>C	ENSP00000497764.1:p.Met279Thr
ENST00000648850.1:c.471T>C
ENST00000648855.1:n.760T>C
ENST00000648870.1:c.836T>C	ENSP00000497599.1:p.Met279Thr
ENST00000648922.1:c.836T>C	ENSP00000497072.1:p.Met279Thr
ENST00000648939.1:c.836T>C	ENSP00000497442.1:p.Met279Thr
ENST00000649097.1:c.836T>C	ENSP00000497551.1:p.Met279Thr
ENST00000649116.1:c.*393T>C	ENSP00000497925.1:n.*393T>C
ENST00000649181.1:c.*198T>C	ENSP00000498150.1:n.*198T>C
ENST00000649242.1:c.*440T>C	ENSP00000497943.1:n.*440T>C
ENST00000649274.1:c.774T>C	ENSP00000497032.1:n.774T>C
ENST00000649518.1:c.*440T>C	ENSP00000498169.1:n.*440T>C
ENST00000649543.1:c.*440T>C	ENSP00000496826.1:n.*440T>C
ENST00000649752.1:c.563T>C	ENSP00000497267.1:p.Met188Thr
ENST00000650076.1:c.211+24300T>C
ENST00000650471.1:c.*280T>C	ENSP00000498027.1:n.*280T>C
ENST00000650604.1:c.263T>C	ENSP00000497105.1:p.Met88Thr
ENST00000373568.6:c.563T>C	ENSP00000362669.2:p.Met188Thr
ENST00000373573.7:c.836T>C	ENSP00000362674.3:p.Met279Thr
ENST00000373583.5:c.164+107424T>C	ENSP00000362685.1:n.164+107424T>C
ENST00000373589.8:c.563T>C	ENSP00000362691.4:p.Met188Thr
ENST00000415409.5:c.758T>C	ENSP00000396424.1:p.Met253Thr
ENST00000436675.5:c.*91T>C	ENSP00000416489.1:n.*91T>C
NM_001166418.1:c.563T>C	NP_001159890.1:p.Met188Thr
NM_018486.2:c.836T>C	NP_060956.1:p.Met279Thr
NR_051952.1:n.1036T>C
XM_011530986.1:c.836T>C	XP_011529288.1:p.Met279Thr
XM_011530987.1:c.836T>C	XP_011529289.1:p.Met279Thr
XM_011530988.1:c.836T>C	XP_011529290.1:p.Met279Thr
XR_938402.1:n.922T>C
XM_011530986.3:c.836T>C	XP_011529288.3:p.Met279Thr
XM_017029640.2:c.758T>C	XP_016885129.2:p.Met253Thr
XM_017029641.2:c.758T>C	XP_016885130.2:p.Met253Thr
XM_017029642.1:c.677T>C	XP_016885131.1:p.Met226Thr
XM_017029643.2:c.650T>C	XP_016885132.1:p.Met217Thr
XM_017029644.2:c.599T>C	XP_016885133.1:p.Met200Thr
XM_017029645.2:c.650T>C	XP_016885134.1:p.Met217Thr
XM_017029646.1:c.449T>C	XP_016885135.1:p.Met150Thr
XM_024452405.1:c.251T>C	XP_024308173.1:p.Met84Thr
XR_001755711.2:n.922T>C
XR_002958779.1:n.922T>C
XR_002958780.1:n.922T>C
XR_002958781.1:n.922T>C
XR_002958782.1:n.898T>C
XR_002958783.1:n.898T>C
XR_938402.3:n.922T>C
NM_018486.3:c.836T>C MANE Select	NP_060956.1:p.Met279Thr
NM_001166418.2:c.563T>C	NP_001159890.1:p.Met188Thr
NR_051952.2:n.776T>C