Canonical Allele Identifier: CA1171085847

Gene: USP1

Linked Data

• dbSNP Id: rs1645184287

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447564_62447565insCTGTTAAACTTTC , CM000663.2:g.62447564_62447565insCTGTTAAACTTTC	GRCh38
NC_000001.10:g.62913235_62913236insCTGTTAAACTTTC , CM000663.1:g.62913235_62913236insCTGTTAAACTTTC	GRCh37
NC_000001.9:g.62685823_62685824insCTGTTAAACTTTC	NCBI36

Transcript Alleles

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