Canonical Allele Identifier: CA620754385

Gene: USP7 USP7-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8963271_8963276del , CM000678.2:g.8963271_8963276del	GRCh38
NC_000016.9:g.9057128_9057133del , CM000678.1:g.9057128_9057133del	GRCh37
NC_000016.8:g.8964629_8964634del	NCBI36
NG_046847.1:g.5224_5229del

Transcript Alleles

HGVS	Amino-acid Change
NM_003470.3:c.25_30del (USP7) MANE Select	NP_003461.2:p.Gln9_Gln10del
ENST00000344836.9:c.25_30del (USP7) MANE Select	ENSP00000343535.4:p.Gln9_Gln10del
NM_003470.2:c.25_30del (USP7)	NP_003461.2:p.Gln9_Gln10del
ENST00000344836.8:c.25_30del (USP7)	ENSP00000343535.4:p.Gln9_Gln10del
ENST00000563961.5:c.25_30del (USP7)	ENSP00000454362.1:p.Gln9_Gln10del
ENST00000569230.5:c.-96+1133_-96+1138del (USP7)	ENSP00000457237.1:n.-96+1133_-96+1138del
ENST00000673704.1:c.184+11833_184+11838del (USP7)	ENSP00000501290.1:n.184+11833_184+11838del
XM_017023652.1:c.25_30del (USP7)	XP_016879141.1:p.Gln9_Gln10del
XR_933049.1:n.1390+377_1390+382del (USP7-AS1)
XR_933049.2:n.756+377_756+382del (USP7-AS1)
XR_933050.1:n.1275+377_1275+382del (USP7-AS1)