Canonical Allele Identifier: CA413638343

Gene: HDAC8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72351739T>C , CM000685.2:g.72351739T>C	GRCh38
NC_000023.10:g.71571589T>C , CM000685.1:g.71571589T>C	GRCh37
NC_000023.9:g.71488314T>C	NCBI36
NG_015851.1:g.226365A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373568.7:c.1105A>G	ENSP00000362669.3:p.Ile369Val
ENST00000373573.9:c.1105A>G MANE Select	ENSP00000362674.3:p.Ile369Val
ENST00000373583.6:c.1027A>G	ENSP00000362685.2:p.Ile343Val
ENST00000373589.9:c.832A>G	ENSP00000362691.4:p.Ile278Val
ENST00000470998.2:c.282A>G
ENST00000647594.1:c.1105A>G	ENSP00000496814.1:p.Ile369Val
ENST00000647613.1:c.*858A>G	ENSP00000497911.1:n.*858A>G
ENST00000647641.1:n.1192A>G
ENST00000647654.1:c.832A>G	ENSP00000497568.1:p.Ile278Val
ENST00000647859.1:c.1105A>G	ENSP00000497530.1:p.Ile369Val
ENST00000647886.1:c.1105A>G	ENSP00000497188.1:p.Ile369Val
ENST00000647980.1:c.1099A>G	ENSP00000498002.1:p.Ile367Val
ENST00000648139.1:c.805A>G	ENSP00000496818.1:p.Ile269Val
ENST00000648276.1:c.489A>G	ENSP00000497619.1:p.Thr163=
ENST00000648452.1:c.1105A>G	ENSP00000497268.1:p.Ile369Val
ENST00000648459.1:c.502A>G	ENSP00000498072.1:p.Ile168Val
ENST00000648504.1:c.1046A>G	ENSP00000497668.1:n.1046A>G
ENST00000648711.1:c.734A>G	ENSP00000498040.1:n.734A>G
ENST00000648731.1:c.1211A>G
ENST00000648834.1:c.*185A>G	ENSP00000497764.1:n.*185A>G
ENST00000648850.1:c.744A>G
ENST00000648855.1:n.1029A>G
ENST00000648922.1:c.1105A>G	ENSP00000497072.1:p.Ile369Val
ENST00000648939.1:c.*185A>G	ENSP00000497442.1:n.*185A>G
ENST00000649097.1:c.1105A>G	ENSP00000497551.1:p.Ile369Val
ENST00000649181.1:c.*467A>G	ENSP00000498150.1:n.*467A>G
ENST00000649274.1:c.1043A>G	ENSP00000497032.1:n.1043A>G
ENST00000649543.1:c.*709A>G	ENSP00000496826.1:n.*709A>G
ENST00000650076.1:c.462A>G
ENST00000650471.1:c.*549A>G	ENSP00000498027.1:n.*549A>G
ENST00000650604.1:c.532A>G	ENSP00000497105.1:p.Ile178Val
ENST00000373573.7:c.1105A>G	ENSP00000362674.3:p.Ile369Val
ENST00000373583.5:c.165-22030A>G	ENSP00000362685.1:n.165-22030A>G
ENST00000373589.8:c.832A>G	ENSP00000362691.4:p.Ile278Val
ENST00000470998.1:n.278A>G
NM_001166418.1:c.832A>G	NP_001159890.1:p.Ile278Val
NM_018486.2:c.1105A>G	NP_060956.1:p.Ile369Val
NR_051952.1:n.1305A>G
XM_011530986.1:c.1105A>G	XP_011529288.1:p.Ile369Val
XR_938402.1:n.1191A>G
XM_011530986.3:c.1105A>G	XP_011529288.3:p.Ile369Val
XM_017029640.2:c.1027A>G	XP_016885129.2:p.Ile343Val
XM_017029641.2:c.1027A>G	XP_016885130.2:p.Ile343Val
XM_017029642.1:c.946A>G	XP_016885131.1:p.Ile316Val
XM_017029643.2:c.919A>G	XP_016885132.1:p.Ile307Val
XM_017029644.2:c.868A>G	XP_016885133.1:p.Ile290Val
XM_017029645.2:c.919A>G	XP_016885134.1:p.Ile307Val
XM_017029646.1:c.718A>G	XP_016885135.1:p.Ile240Val
XM_024452405.1:c.520A>G	XP_024308173.1:p.Ile174Val
XR_001755711.2:n.1191A>G
XR_002958779.1:n.1287A>G
XR_002958780.1:n.1195A>G
XR_002958781.1:n.1195A>G
XR_002958783.1:n.1171A>G
XR_938402.3:n.1191A>G
NM_018486.3:c.1105A>G MANE Select	NP_060956.1:p.Ile369Val
NM_001166418.2:c.832A>G	NP_001159890.1:p.Ile278Val
NR_051952.2:n.1045A>G