Canonical Allele Identifier: CA490561930

Gene: USP8

Linked Data

• MyVariant Identifiers: chr15:g.50782702A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50490505A>T , CM000677.2:g.50490505A>T	GRCh38
NC_000015.9:g.50782702A>T , CM000677.1:g.50782702A>T	GRCh37
NC_000015.8:g.48569994A>T	NCBI36
NG_047101.1:g.71129A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307179.9:c.2214A>T MANE Select	ENSP00000302239.4:p.Pro738=
ENST00000307179.8:c.2214A>T	ENSP00000302239.4:p.Pro738=
ENST00000396444.7:c.2214A>T	ENSP00000379721.3:p.Pro738=
ENST00000425032.7:c.1896A>T	ENSP00000412682.3:p.Pro632=
NM_001128610.2:c.2214A>T	NP_001122082.1:p.Pro738=
NM_001283049.1:c.1896A>T	NP_001269978.1:p.Pro632=
NM_005154.4:c.2214A>T	NP_005145.3:p.Pro738=
XM_006720761.2:c.2214A>T	XP_006720824.1:p.Pro738=
XM_006720762.2:c.2127A>T	XP_006720825.1:p.Pro709=
XM_011522193.1:c.2214A>T	XP_011520495.1:p.Pro738=
XM_011522194.1:c.1542A>T	XP_011520496.1:p.Pro514=
XM_006720761.3:c.2214A>T	XP_006720824.1:p.Pro738=
XM_006720762.3:c.2127A>T	XP_006720825.1:p.Pro709=
XM_011522193.3:c.2214A>T	XP_011520495.1:p.Pro738=
XM_017022718.1:c.2127A>T	XP_016878207.1:p.Pro709=
XM_017022719.2:c.2127A>T	XP_016878208.1:p.Pro709=
XM_017022720.2:c.2127A>T	XP_016878209.1:p.Pro709=
XM_017022721.2:c.1644A>T	XP_016878210.1:p.Pro548=
XM_017022722.1:c.1644A>T	XP_016878211.1:p.Pro548=
XM_024450098.1:c.1644A>T	XP_024305866.1:p.Pro548=
NM_005154.5:c.2214A>T MANE Select	NP_005145.3:p.Pro738=
NM_001128610.3:c.2214A>T	NP_001122082.1:p.Pro738=
NM_001283049.2:c.1896A>T	NP_001269978.1:p.Pro632=