Canonical Allele Identifier: CA413638295

Gene: HDAC8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72330071G>T , CM000685.2:g.72330071G>T	GRCh38
NC_000023.10:g.71549921G>T , CM000685.1:g.71549921G>T	GRCh37
NC_000023.9:g.71466646G>T	NCBI36
NG_015851.1:g.248033C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018486.3:c.1117C>A MANE Select	NP_060956.1:p.Leu373Met
ENST00000373573.9:c.1117C>A MANE Select	ENSP00000362674.3:p.Leu373Met
NM_001166418.1:c.844C>A	NP_001159890.1:p.Leu282Met
NM_001166418.2:c.844C>A	NP_001159890.1:p.Leu282Met
NM_018486.2:c.1117C>A	NP_060956.1:p.Leu373Met
NR_051952.1:n.1317C>A
NR_051952.2:n.1057C>A
ENST00000373573.7:c.1117C>A	ENSP00000362674.3:p.Leu373Met
ENST00000373583.5:c.165-362C>A	ENSP00000362685.1:n.165-362C>A
ENST00000373583.6:c.1039C>A	ENSP00000362685.2:p.Leu347Met
ENST00000373589.8:c.844C>A	ENSP00000362691.4:p.Leu282Met
ENST00000373589.9:c.844C>A	ENSP00000362691.4:p.Leu282Met
ENST00000647594.1:c.*56C>A	ENSP00000496814.1:n.*56C>A
ENST00000647613.1:c.*864+21662C>A	ENSP00000497911.1:n.*864+21662C>A
ENST00000647654.1:c.922C>A	ENSP00000497568.1:p.Leu308Met
ENST00000647859.1:c.*795C>A	ENSP00000497530.1:n.*795C>A
ENST00000647886.1:c.1195C>A	ENSP00000497188.1:p.Leu399Met
ENST00000647980.1:c.1111C>A	ENSP00000498002.1:p.Leu371Met
ENST00000648276.1:c.501C>A	ENSP00000497619.1:p.Ile167=
ENST00000648452.1:c.1228C>A	ENSP00000497268.1:p.Leu410Met
ENST00000648459.1:c.514C>A	ENSP00000498072.1:p.Leu172Met
ENST00000648504.1:c.1244C>A	ENSP00000497668.1:n.1244C>A
ENST00000648731.1:c.1223C>A
ENST00000648850.1:c.756C>A
ENST00000648855.1:n.1227C>A
ENST00000648922.1:c.1111+21662C>A	ENSP00000497072.1:n.1111+21662C>A
ENST00000648939.1:c.*197C>A	ENSP00000497442.1:n.*197C>A
ENST00000649097.1:c.*224C>A	ENSP00000497551.1:n.*224C>A
ENST00000649181.1:c.*479C>A	ENSP00000498150.1:n.*479C>A
ENST00000649274.1:c.1133C>A	ENSP00000497032.1:n.1133C>A
ENST00000650076.1:c.474C>A
ENST00000650471.1:c.*561C>A	ENSP00000498027.1:n.*561C>A
ENST00000650477.1:n.173C>A
ENST00000650604.1:c.544C>A	ENSP00000497105.1:p.Leu182Met
XM_011530986.1:c.1195C>A	XP_011529288.1:p.Leu399Met
XM_011530986.3:c.1195C>A	XP_011529288.3:p.Leu399Met
XM_017029640.2:c.1117C>A	XP_016885129.2:p.Leu373Met
XM_017029641.2:c.1039C>A	XP_016885130.2:p.Leu347Met
XM_017029642.1:c.1036C>A	XP_016885131.1:p.Leu346Met
XM_017029643.2:c.1009C>A	XP_016885132.1:p.Leu337Met
XM_017029644.2:c.958C>A	XP_016885133.1:p.Leu320Met
XM_017029645.2:c.931C>A	XP_016885134.1:p.Leu311Met
XM_017029646.1:c.808C>A	XP_016885135.1:p.Leu270Met
XM_024452405.1:c.610C>A	XP_024308173.1:p.Leu204Met
XR_001755711.2:n.1389C>A
XR_002958780.1:n.1207C>A
XR_002958781.1:n.1393C>A
XR_938402.1:n.1264C>A
XR_938402.3:n.1264C>A