Canonical Allele Identifier: CA1171085729
Gene: USP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447194_62447202delinsCTCTAATAA , CM000663.2:g.62447194_62447202delinsCTCTAATAA GRCh38
NC_000001.10:g.62912865_62912873delinsCTCTAATAA , CM000663.1:g.62912865_62912873delinsCTCTAATAA GRCh37
NC_000001.9:g.62685453_62685461delinsCTCTAATAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339950.5:c.1250-147_1250-139delinsCTCTAATAA MANE Select ENSP00000343526.4:n.1250-147_1250-139deli...
ENST00000339950.4:c.1250-147_1250-139delinsCTCTAATAA ENSP00000343526.4:n.1250-147_1250-139deli...
ENST00000371146.5:c.1250-147_1250-139delinsCTCTAATAA ENSP00000360188.1:n.1250-147_1250-139deli...
NM_001017415.1:c.1250-147_1250-139delinsCTCTAATAA NP_001017415.1:n.1250-147_1250-139delinsC...
NM_001017416.1:c.1250-147_1250-139delinsCTCTAATAA NP_001017416.1:n.1250-147_1250-139delinsC...
NM_003368.4:c.1250-147_1250-139delinsCTCTAATAA NP_003359.3:n.1250-147_1250-139delinsCTCT...
NM_003368.5:c.1250-147_1250-139delinsCTCTAATAA MANE Select NP_003359.3:n.1250-147_1250-139delinsCTCT...
NM_001017415.2:c.1250-147_1250-139delinsCTCTAATAA NP_001017415.1:n.1250-147_1250-139delinsC...
NM_001017416.2:c.1250-147_1250-139delinsCTCTAATAA NP_001017416.1:n.1250-147_1250-139delinsC...