Canonical Allele Identifier: CA2645983187
Gene: USP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447257_62447261del , CM000663.2:g.62447257_62447261del GRCh38
NC_000001.10:g.62912928_62912932del , CM000663.1:g.62912928_62912932del GRCh37
NC_000001.9:g.62685516_62685520del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1250-84_1250-80del MANE Select ENSP00000343526.4:n.1250-84_1250-80del
ENST00000339950.4:c.1250-84_1250-80del ENSP00000343526.4:n.1250-84_1250-80del
ENST00000371146.5:c.1250-84_1250-80del ENSP00000360188.1:n.1250-84_1250-80del
NM_001017415.1:c.1250-84_1250-80del NP_001017415.1:n.1250-84_1250-80del
NM_001017416.1:c.1250-84_1250-80del NP_001017416.1:n.1250-84_1250-80del
NM_003368.4:c.1250-84_1250-80del NP_003359.3:n.1250-84_1250-80del
NM_003368.5:c.1250-84_1250-80del MANE Select NP_003359.3:n.1250-84_1250-80del
NM_001017415.2:c.1250-84_1250-80del NP_001017415.1:n.1250-84_1250-80del
NM_001017416.2:c.1250-84_1250-80del NP_001017416.1:n.1250-84_1250-80del