Canonical Allele Identifier: CA737668855
Gene: USP1 HGNC NCBI

Linked Data

dbSNP Id: rs1181605490
MyVariant Identifiers: chr1:g.62912866_62912873del (hg19) chr1:g.62447195_62447202del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447195_62447202del , CM000663.2:g.62447195_62447202del GRCh38
NC_000001.10:g.62912866_62912873del , CM000663.1:g.62912866_62912873del GRCh37
NC_000001.9:g.62685454_62685461del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339950.5:c.1250-146_1250-139del MANE Select ENSP00000343526.4:n.1250-146_1250-139del
ENST00000339950.4:c.1250-146_1250-139del ENSP00000343526.4:n.1250-146_1250-139del
ENST00000371146.5:c.1250-146_1250-139del ENSP00000360188.1:n.1250-146_1250-139del
NM_001017415.1:c.1250-146_1250-139del NP_001017415.1:n.1250-146_1250-139del
NM_001017416.1:c.1250-146_1250-139del NP_001017416.1:n.1250-146_1250-139del
NM_003368.4:c.1250-146_1250-139del NP_003359.3:n.1250-146_1250-139del
NM_003368.5:c.1250-146_1250-139del MANE Select NP_003359.3:n.1250-146_1250-139del
NM_001017415.2:c.1250-146_1250-139del NP_001017415.1:n.1250-146_1250-139del
NM_001017416.2:c.1250-146_1250-139del NP_001017416.1:n.1250-146_1250-139del
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