Canonical Allele Identifier: CA2176424996

Gene: USP8

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50490644_50490659delinsCCGTTATTATTTACCA , CM000677.2:g.50490644_50490659delinsCCGTTATTATTTACCA	GRCh38
NC_000015.9:g.50782841_50782856delinsCCGTTATTATTTACCA , CM000677.1:g.50782841_50782856delinsCCGTTATTATTTACCA	GRCh37
NC_000015.8:g.48570133_48570148delinsCCGTTATTATTTACCA	NCBI36
NG_047101.1:g.71268_71283delinsCCGTTATTATTTACCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307179.9:c.2234+119_2234+134delinsCCGTTATTATTTACCA MANE Select	ENSP00000302239.4:n.2234+119_2234+134delinsCCGTTATTATTTACCA
ENST00000307179.8:c.2234+119_2234+134delinsCCGTTATTATTTACCA	ENSP00000302239.4:n.2234+119_2234+134delinsCCGTTATTATTTACCA
ENST00000396444.7:c.2234+119_2234+134delinsCCGTTATTATTTACCA	ENSP00000379721.3:n.2234+119_2234+134delinsCCGTTATTATTTACCA
ENST00000425032.7:c.1916+119_1916+134delinsCCGTTATTATTTACCA	ENSP00000412682.3:n.1916+119_1916+134delinsCCGTTATTATTTACCA
NM_001128610.2:c.2234+119_2234+134delinsCCGTTATTATTTACCA	NP_001122082.1:n.2234+119_2234+134delinsCCGTTATTATTTACCA
NM_001283049.1:c.1916+119_1916+134delinsCCGTTATTATTTACCA	NP_001269978.1:n.1916+119_1916+134delinsCCGTTATTATTTACCA
NM_005154.4:c.2234+119_2234+134delinsCCGTTATTATTTACCA	NP_005145.3:n.2234+119_2234+134delinsCCGTTATTATTTACCA
XM_006720761.2:c.2234+119_2234+134delinsCCGTTATTATTTACCA	XP_006720824.1:n.2234+119_2234+134delinsCCGTTATTATTTACCA
XM_006720762.2:c.2147+119_2147+134delinsCCGTTATTATTTACCA	XP_006720825.1:n.2147+119_2147+134delinsCCGTTATTATTTACCA
XM_011522193.1:c.2234+119_2234+134delinsCCGTTATTATTTACCA	XP_011520495.1:n.2234+119_2234+134delinsCCGTTATTATTTACCA
XM_011522194.1:c.1562+119_1562+134delinsCCGTTATTATTTACCA	XP_011520496.1:n.1562+119_1562+134delinsCCGTTATTATTTACCA
XM_006720761.3:c.2234+119_2234+134delinsCCGTTATTATTTACCA	XP_006720824.1:n.2234+119_2234+134delinsCCGTTATTATTTACCA
XM_006720762.3:c.2147+119_2147+134delinsCCGTTATTATTTACCA	XP_006720825.1:n.2147+119_2147+134delinsCCGTTATTATTTACCA
XM_011522193.3:c.2234+119_2234+134delinsCCGTTATTATTTACCA	XP_011520495.1:n.2234+119_2234+134delinsCCGTTATTATTTACCA
XM_017022718.1:c.2147+119_2147+134delinsCCGTTATTATTTACCA	XP_016878207.1:n.2147+119_2147+134delinsCCGTTATTATTTACCA
XM_017022719.2:c.2147+119_2147+134delinsCCGTTATTATTTACCA	XP_016878208.1:n.2147+119_2147+134delinsCCGTTATTATTTACCA
XM_017022720.2:c.2147+119_2147+134delinsCCGTTATTATTTACCA	XP_016878209.1:n.2147+119_2147+134delinsCCGTTATTATTTACCA
XM_017022721.2:c.1664+119_1664+134delinsCCGTTATTATTTACCA	XP_016878210.1:n.1664+119_1664+134delinsCCGTTATTATTTACCA
XM_017022722.1:c.1664+119_1664+134delinsCCGTTATTATTTACCA	XP_016878211.1:n.1664+119_1664+134delinsCCGTTATTATTTACCA
XM_024450098.1:c.1664+119_1664+134delinsCCGTTATTATTTACCA	XP_024305866.1:n.1664+119_1664+134delinsCCGTTATTATTTACCA
NM_005154.5:c.2234+119_2234+134delinsCCGTTATTATTTACCA MANE Select	NP_005145.3:n.2234+119_2234+134delinsCCGTTATTATTTACCA
NM_001128610.3:c.2234+119_2234+134delinsCCGTTATTATTTACCA	NP_001122082.1:n.2234+119_2234+134delinsCCGTTATTATTTACCA
NM_001283049.2:c.1916+119_1916+134delinsCCGTTATTATTTACCA	NP_001269978.1:n.1916+119_1916+134delinsCCGTTATTATTTACCA