Canonical Allele Identifier: CA413638393

Gene: HDAC8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72351759A>G , CM000685.2:g.72351759A>G	GRCh38
NC_000023.10:g.71571609A>G , CM000685.1:g.71571609A>G	GRCh37
NC_000023.9:g.71488334A>G	NCBI36
NG_015851.1:g.226345T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018486.3:c.1085T>C MANE Select	NP_060956.1:p.Ile362Thr
ENST00000373573.9:c.1085T>C MANE Select	ENSP00000362674.3:p.Ile362Thr
NM_001166418.1:c.812T>C	NP_001159890.1:p.Ile271Thr
NM_001166418.2:c.812T>C	NP_001159890.1:p.Ile271Thr
NM_018486.2:c.1085T>C	NP_060956.1:p.Ile362Thr
NR_051952.1:n.1285T>C
NR_051952.2:n.1025T>C
ENST00000373568.7:c.1085T>C	ENSP00000362669.3:p.Ile362Thr
ENST00000373573.7:c.1085T>C	ENSP00000362674.3:p.Ile362Thr
ENST00000373583.5:c.165-22050T>C	ENSP00000362685.1:n.165-22050T>C
ENST00000373583.6:c.1007T>C	ENSP00000362685.2:p.Ile336Thr
ENST00000373589.8:c.812T>C	ENSP00000362691.4:p.Ile271Thr
ENST00000373589.9:c.812T>C	ENSP00000362691.4:p.Ile271Thr
ENST00000470998.1:n.258T>C
ENST00000470998.2:c.262T>C
ENST00000647594.1:c.1085T>C	ENSP00000496814.1:p.Ile362Thr
ENST00000647613.1:c.*838T>C	ENSP00000497911.1:n.*838T>C
ENST00000647641.1:n.1172T>C
ENST00000647654.1:c.812T>C	ENSP00000497568.1:p.Ile271Thr
ENST00000647859.1:c.1085T>C	ENSP00000497530.1:p.Ile362Thr
ENST00000647886.1:c.1085T>C	ENSP00000497188.1:p.Ile362Thr
ENST00000647980.1:c.1079T>C	ENSP00000498002.1:p.Ile360Thr
ENST00000648139.1:c.785T>C	ENSP00000496818.1:p.Ile262Thr
ENST00000648276.1:c.469T>C	ENSP00000497619.1:p.Ser157Pro
ENST00000648452.1:c.1085T>C	ENSP00000497268.1:p.Ile362Thr
ENST00000648459.1:c.482T>C	ENSP00000498072.1:p.Ile161Thr
ENST00000648504.1:c.1026T>C	ENSP00000497668.1:n.1026T>C
ENST00000648711.1:c.714T>C	ENSP00000498040.1:n.714T>C
ENST00000648731.1:c.1191T>C
ENST00000648834.1:c.*165T>C	ENSP00000497764.1:n.*165T>C
ENST00000648850.1:c.724T>C
ENST00000648855.1:n.1009T>C
ENST00000648922.1:c.1085T>C	ENSP00000497072.1:p.Ile362Thr
ENST00000648939.1:c.*165T>C	ENSP00000497442.1:n.*165T>C
ENST00000649097.1:c.1085T>C	ENSP00000497551.1:p.Ile362Thr
ENST00000649181.1:c.*447T>C	ENSP00000498150.1:n.*447T>C
ENST00000649274.1:c.1023T>C	ENSP00000497032.1:n.1023T>C
ENST00000649543.1:c.*689T>C	ENSP00000496826.1:n.*689T>C
ENST00000650076.1:c.442T>C
ENST00000650471.1:c.*529T>C	ENSP00000498027.1:n.*529T>C
ENST00000650604.1:c.512T>C	ENSP00000497105.1:p.Ile171Thr
XM_011530986.1:c.1085T>C	XP_011529288.1:p.Ile362Thr
XM_011530986.3:c.1085T>C	XP_011529288.3:p.Ile362Thr
XM_017029640.2:c.1007T>C	XP_016885129.2:p.Ile336Thr
XM_017029641.2:c.1007T>C	XP_016885130.2:p.Ile336Thr
XM_017029642.1:c.926T>C	XP_016885131.1:p.Ile309Thr
XM_017029643.2:c.899T>C	XP_016885132.1:p.Ile300Thr
XM_017029644.2:c.848T>C	XP_016885133.1:p.Ile283Thr
XM_017029645.2:c.899T>C	XP_016885134.1:p.Ile300Thr
XM_017029646.1:c.698T>C	XP_016885135.1:p.Ile233Thr
XM_024452405.1:c.500T>C	XP_024308173.1:p.Ile167Thr
XR_001755711.2:n.1171T>C
XR_002958779.1:n.1267T>C
XR_002958780.1:n.1175T>C
XR_002958781.1:n.1175T>C
XR_002958783.1:n.1151T>C
XR_938402.1:n.1171T>C
XR_938402.3:n.1171T>C