Canonical Allele Identifier: CA392398997

Gene: USP8

Linked Data

• MyVariant Identifiers: chr15:g.50782598G>A (hg19) ; chr15:g.50490401G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50490401G>A , CM000677.2:g.50490401G>A	GRCh38
NC_000015.9:g.50782598G>A , CM000677.1:g.50782598G>A	GRCh37
NC_000015.8:g.48569890G>A	NCBI36
NG_047101.1:g.71025G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307179.9:c.2110G>A MANE Select	ENSP00000302239.4:p.Ala704Thr
ENST00000307179.8:c.2110G>A	ENSP00000302239.4:p.Ala704Thr
ENST00000396444.7:c.2110G>A	ENSP00000379721.3:p.Ala704Thr
ENST00000425032.7:c.1792G>A	ENSP00000412682.3:p.Ala598Thr
ENST00000561206.1:n.527G>A
NM_001128610.2:c.2110G>A	NP_001122082.1:p.Ala704Thr
NM_001283049.1:c.1792G>A	NP_001269978.1:p.Ala598Thr
NM_005154.4:c.2110G>A	NP_005145.3:p.Ala704Thr
XM_006720761.2:c.2110G>A	XP_006720824.1:p.Ala704Thr
XM_006720762.2:c.2023G>A	XP_006720825.1:p.Ala675Thr
XM_011522193.1:c.2110G>A	XP_011520495.1:p.Ala704Thr
XM_011522194.1:c.1438G>A	XP_011520496.1:p.Ala480Thr
XM_006720761.3:c.2110G>A	XP_006720824.1:p.Ala704Thr
XM_006720762.3:c.2023G>A	XP_006720825.1:p.Ala675Thr
XM_011522193.3:c.2110G>A	XP_011520495.1:p.Ala704Thr
XM_017022718.1:c.2023G>A	XP_016878207.1:p.Ala675Thr
XM_017022719.2:c.2023G>A	XP_016878208.1:p.Ala675Thr
XM_017022720.2:c.2023G>A	XP_016878209.1:p.Ala675Thr
XM_017022721.2:c.1540G>A	XP_016878210.1:p.Ala514Thr
XM_017022722.1:c.1540G>A	XP_016878211.1:p.Ala514Thr
XM_024450098.1:c.1540G>A	XP_024305866.1:p.Ala514Thr
NM_005154.5:c.2110G>A MANE Select	NP_005145.3:p.Ala704Thr
NM_001128610.3:c.2110G>A	NP_001122082.1:p.Ala704Thr
NM_001283049.2:c.1792G>A	NP_001269978.1:p.Ala598Thr