Canonical Allele Identifier: CA1171085758
Gene: USP1 HGNC NCBI

Linked Data

dbSNP Id: rs1645182223
gnomAD v4: 1-62447257-CTTTA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447262_62447265del , CM000663.2:g.62447262_62447265del GRCh38
NC_000001.10:g.62912933_62912936del , CM000663.1:g.62912933_62912936del GRCh37
NC_000001.9:g.62685521_62685524del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339950.5:c.1250-79_1250-76del MANE Select ENSP00000343526.4:n.1250-79_1250-76del
ENST00000339950.4:c.1250-79_1250-76del ENSP00000343526.4:n.1250-79_1250-76del
ENST00000371146.5:c.1250-79_1250-76del ENSP00000360188.1:n.1250-79_1250-76del
NM_001017415.1:c.1250-79_1250-76del NP_001017415.1:n.1250-79_1250-76del
NM_001017416.1:c.1250-79_1250-76del NP_001017416.1:n.1250-79_1250-76del
NM_003368.4:c.1250-79_1250-76del NP_003359.3:n.1250-79_1250-76del
NM_003368.5:c.1250-79_1250-76del MANE Select NP_003359.3:n.1250-79_1250-76del
NM_001017415.2:c.1250-79_1250-76del NP_001017415.1:n.1250-79_1250-76del
NM_001017416.2:c.1250-79_1250-76del NP_001017416.1:n.1250-79_1250-76del
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