Canonical Allele Identifier: CA2645983223
Gene: USP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447293_62447310del , CM000663.2:g.62447293_62447310del GRCh38
NC_000001.10:g.62912964_62912981del , CM000663.1:g.62912964_62912981del GRCh37
NC_000001.9:g.62685552_62685569del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1250-48_1250-31del MANE Select ENSP00000343526.4:n.1250-48_1250-31del
ENST00000339950.4:c.1250-48_1250-31del ENSP00000343526.4:n.1250-48_1250-31del
ENST00000371146.5:c.1250-48_1250-31del ENSP00000360188.1:n.1250-48_1250-31del
NM_001017415.1:c.1250-48_1250-31del NP_001017415.1:n.1250-48_1250-31del
NM_001017416.1:c.1250-48_1250-31del NP_001017416.1:n.1250-48_1250-31del
NM_003368.4:c.1250-48_1250-31del NP_003359.3:n.1250-48_1250-31del
NM_003368.5:c.1250-48_1250-31del MANE Select NP_003359.3:n.1250-48_1250-31del
NM_001017415.2:c.1250-48_1250-31del NP_001017415.1:n.1250-48_1250-31del
NM_001017416.2:c.1250-48_1250-31del NP_001017416.1:n.1250-48_1250-31del