Canonical Allele Identifier: CA1171085845

Gene: USP1

Linked Data

• dbSNP Id: rs1645184270

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447564_62447565insCTGTT , CM000663.2:g.62447564_62447565insCTGTT	GRCh38
NC_000001.10:g.62913235_62913236insCTGTT , CM000663.1:g.62913235_62913236insCTGTT	GRCh37
NC_000001.9:g.62685823_62685824insCTGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+53_1420+54insCTGTT MANE Select	ENSP00000343526.4:n.1420+53_1420+54insCTGTT
ENST00000339950.4:c.1420+53_1420+54insCTGTT	ENSP00000343526.4:n.1420+53_1420+54insCTGTT
ENST00000371146.5:c.1420+53_1420+54insCTGTT	ENSP00000360188.1:n.1420+53_1420+54insCTGTT
NM_001017415.1:c.1420+53_1420+54insCTGTT	NP_001017415.1:n.1420+53_1420+54insCTGTT
NM_001017416.1:c.1420+53_1420+54insCTGTT	NP_001017416.1:n.1420+53_1420+54insCTGTT
NM_003368.4:c.1420+53_1420+54insCTGTT	NP_003359.3:n.1420+53_1420+54insCTGTT
NM_003368.5:c.1420+53_1420+54insCTGTT MANE Select	NP_003359.3:n.1420+53_1420+54insCTGTT
NM_001017415.2:c.1420+53_1420+54insCTGTT	NP_001017415.1:n.1420+53_1420+54insCTGTT
NM_001017416.2:c.1420+53_1420+54insCTGTT	NP_001017416.1:n.1420+53_1420+54insCTGTT