Canonical Allele Identifier: CA645580776
Gene: USP8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50490443_50490449delinsA , CM000677.2:g.50490443_50490449delinsA GRCh38
NC_000015.9:g.50782640_50782646delinsA , CM000677.1:g.50782640_50782646delinsA GRCh37
NC_000015.8:g.48569932_48569938delinsA NCBI36
NG_047101.1:g.71067_71073delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307179.9:c.2152_2158delinsA MANE Select ENSP00000302239.4:p.Ser718_Pro720delinsThr
ENST00000307179.8:c.2152_2158delinsA ENSP00000302239.4:p.Ser718_Pro720delinsThr
ENST00000396444.7:c.2152_2158delinsA ENSP00000379721.3:p.Ser718_Pro720delinsThr
ENST00000425032.7:c.1834_1840delinsA ENSP00000412682.3:p.Ser612_Pro614delinsThr
NM_001128610.2:c.2152_2158delinsA NP_001122082.1:p.Ser718_Pro720delinsThr
NM_001283049.1:c.1834_1840delinsA NP_001269978.1:p.Ser612_Pro614delinsThr
NM_005154.4:c.2152_2158delinsA NP_005145.3:p.Ser718_Pro720delinsThr
XM_006720761.2:c.2152_2158delinsA XP_006720824.1:p.Ser718_Pro720delinsThr
XM_006720762.2:c.2065_2071delinsA XP_006720825.1:p.Ser689_Pro691delinsThr
XM_011522193.1:c.2152_2158delinsA XP_011520495.1:p.Ser718_Pro720delinsThr
XM_011522194.1:c.1480_1486delinsA XP_011520496.1:p.Ser494_Pro496delinsThr
XM_006720761.3:c.2152_2158delinsA XP_006720824.1:p.Ser718_Pro720delinsThr
XM_006720762.3:c.2065_2071delinsA XP_006720825.1:p.Ser689_Pro691delinsThr
XM_011522193.3:c.2152_2158delinsA XP_011520495.1:p.Ser718_Pro720delinsThr
XM_017022718.1:c.2065_2071delinsA XP_016878207.1:p.Ser689_Pro691delinsThr
XM_017022719.2:c.2065_2071delinsA XP_016878208.1:p.Ser689_Pro691delinsThr
XM_017022720.2:c.2065_2071delinsA XP_016878209.1:p.Ser689_Pro691delinsThr
XM_017022721.2:c.1582_1588delinsA XP_016878210.1:p.Ser528_Pro530delinsThr
XM_017022722.1:c.1582_1588delinsA XP_016878211.1:p.Ser528_Pro530delinsThr
XM_024450098.1:c.1582_1588delinsA XP_024305866.1:p.Ser528_Pro530delinsThr
NM_005154.5:c.2152_2158delinsA MANE Select NP_005145.3:p.Ser718_Pro720delinsThr
NM_001128610.3:c.2152_2158delinsA NP_001122082.1:p.Ser718_Pro720delinsThr
NM_001283049.2:c.1834_1840delinsA NP_001269978.1:p.Ser612_Pro614delinsThr