Canonical Allele Identifier: CA2176424893

Gene: USP8

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50490383G= , CM000677.2:g.50490383G=	GRCh38
NC_000015.9:g.50782580G= , CM000677.1:g.50782580G=	GRCh37
NC_000015.8:g.48569872G=	NCBI36
NG_047101.1:g.71007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307179.9:c.2092G= MANE Select	ENSP00000302239.4:p.Ala698=
ENST00000307179.8:c.2092G=	ENSP00000302239.4:p.Ala698=
ENST00000396444.7:c.2092G=	ENSP00000379721.3:p.Ala698=
ENST00000425032.7:c.1774G=	ENSP00000412682.3:p.Ala592=
ENST00000561206.1:n.509G=
NM_001128610.2:c.2092G=	NP_001122082.1:p.Ala698=
NM_001283049.1:c.1774G=	NP_001269978.1:p.Ala592=
NM_005154.4:c.2092G=	NP_005145.3:p.Ala698=
XM_006720761.2:c.2092G=	XP_006720824.1:p.Ala698=
XM_006720762.2:c.2005G=	XP_006720825.1:p.Ala669=
XM_011522193.1:c.2092G=	XP_011520495.1:p.Ala698=
XM_011522194.1:c.1420G=	XP_011520496.1:p.Ala474=
XM_006720761.3:c.2092G=	XP_006720824.1:p.Ala698=
XM_006720762.3:c.2005G=	XP_006720825.1:p.Ala669=
XM_011522193.3:c.2092G=	XP_011520495.1:p.Ala698=
XM_017022718.1:c.2005G=	XP_016878207.1:p.Ala669=
XM_017022719.2:c.2005G=	XP_016878208.1:p.Ala669=
XM_017022720.2:c.2005G=	XP_016878209.1:p.Ala669=
XM_017022721.2:c.1522G=	XP_016878210.1:p.Ala508=
XM_017022722.1:c.1522G=	XP_016878211.1:p.Ala508=
XM_024450098.1:c.1522G=	XP_024305866.1:p.Ala508=
NM_005154.5:c.2092G= MANE Select	NP_005145.3:p.Ala698=
NM_001128610.3:c.2092G=	NP_001122082.1:p.Ala698=
NM_001283049.2:c.1774G=	NP_001269978.1:p.Ala592=