Canonical Allele Identifier: CA2645983484
Gene: USP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447585_62447587del , CM000663.2:g.62447585_62447587del GRCh38
NC_000001.10:g.62913256_62913258del , CM000663.1:g.62913256_62913258del GRCh37
NC_000001.9:g.62685844_62685846del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1420+74_1420+76del MANE Select ENSP00000343526.4:n.1420+74_1420+76del
ENST00000339950.4:c.1420+74_1420+76del ENSP00000343526.4:n.1420+74_1420+76del
ENST00000371146.5:c.1420+74_1420+76del ENSP00000360188.1:n.1420+74_1420+76del
NM_001017415.1:c.1420+74_1420+76del NP_001017415.1:n.1420+74_1420+76del
NM_001017416.1:c.1420+74_1420+76del NP_001017416.1:n.1420+74_1420+76del
NM_003368.4:c.1420+74_1420+76del NP_003359.3:n.1420+74_1420+76del
NM_003368.5:c.1420+74_1420+76del MANE Select NP_003359.3:n.1420+74_1420+76del
NM_001017415.2:c.1420+74_1420+76del NP_001017415.1:n.1420+74_1420+76del
NM_001017416.2:c.1420+74_1420+76del NP_001017416.1:n.1420+74_1420+76del