Canonical Allele Identifier: CA2176425017

Gene: USP8

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50490688_50490691delinsATGT , CM000677.2:g.50490688_50490691delinsATGT	GRCh38
NC_000015.9:g.50782885_50782888delinsATGT , CM000677.1:g.50782885_50782888delinsATGT	GRCh37
NC_000015.8:g.48570177_48570180delinsATGT	NCBI36
NG_047101.1:g.71312_71315delinsATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307179.9:c.2234+163_2234+166delinsATGT MANE Select	ENSP00000302239.4:n.2234+163_2234+166delinsATGT
ENST00000307179.8:c.2234+163_2234+166delinsATGT	ENSP00000302239.4:n.2234+163_2234+166delinsATGT
ENST00000396444.7:c.2234+163_2234+166delinsATGT	ENSP00000379721.3:n.2234+163_2234+166delinsATGT
ENST00000425032.7:c.1916+163_1916+166delinsATGT	ENSP00000412682.3:n.1916+163_1916+166delinsATGT
NM_001128610.2:c.2234+163_2234+166delinsATGT	NP_001122082.1:n.2234+163_2234+166delinsATGT
NM_001283049.1:c.1916+163_1916+166delinsATGT	NP_001269978.1:n.1916+163_1916+166delinsATGT
NM_005154.4:c.2234+163_2234+166delinsATGT	NP_005145.3:n.2234+163_2234+166delinsATGT
XM_006720761.2:c.2234+163_2234+166delinsATGT	XP_006720824.1:n.2234+163_2234+166delinsATGT
XM_006720762.2:c.2147+163_2147+166delinsATGT	XP_006720825.1:n.2147+163_2147+166delinsATGT
XM_011522193.1:c.2234+163_2234+166delinsATGT	XP_011520495.1:n.2234+163_2234+166delinsATGT
XM_011522194.1:c.1562+163_1562+166delinsATGT	XP_011520496.1:n.1562+163_1562+166delinsATGT
XM_006720761.3:c.2234+163_2234+166delinsATGT	XP_006720824.1:n.2234+163_2234+166delinsATGT
XM_006720762.3:c.2147+163_2147+166delinsATGT	XP_006720825.1:n.2147+163_2147+166delinsATGT
XM_011522193.3:c.2234+163_2234+166delinsATGT	XP_011520495.1:n.2234+163_2234+166delinsATGT
XM_017022718.1:c.2147+163_2147+166delinsATGT	XP_016878207.1:n.2147+163_2147+166delinsATGT
XM_017022719.2:c.2147+163_2147+166delinsATGT	XP_016878208.1:n.2147+163_2147+166delinsATGT
XM_017022720.2:c.2147+163_2147+166delinsATGT	XP_016878209.1:n.2147+163_2147+166delinsATGT
XM_017022721.2:c.1664+163_1664+166delinsATGT	XP_016878210.1:n.1664+163_1664+166delinsATGT
XM_017022722.1:c.1664+163_1664+166delinsATGT	XP_016878211.1:n.1664+163_1664+166delinsATGT
XM_024450098.1:c.1664+163_1664+166delinsATGT	XP_024305866.1:n.1664+163_1664+166delinsATGT
NM_005154.5:c.2234+163_2234+166delinsATGT MANE Select	NP_005145.3:n.2234+163_2234+166delinsATGT
NM_001128610.3:c.2234+163_2234+166delinsATGT	NP_001122082.1:n.2234+163_2234+166delinsATGT
NM_001283049.2:c.1916+163_1916+166delinsATGT	NP_001269978.1:n.1916+163_1916+166delinsATGT