Canonical Allele Identifier: CA1171085846
Gene: USP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447564T= , CM000663.2:g.62447564T= GRCh38
NC_000001.10:g.62913235T= , CM000663.1:g.62913235T= GRCh37
NC_000001.9:g.62685823T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1420+53T= MANE Select ENSP00000343526.4:n.1420+53T=
ENST00000339950.4:c.1420+53T= ENSP00000343526.4:n.1420+53T=
ENST00000371146.5:c.1420+53T= ENSP00000360188.1:n.1420+53T=
NM_001017415.1:c.1420+53T= NP_001017415.1:n.1420+53T=
NM_001017416.1:c.1420+53T= NP_001017416.1:n.1420+53T=
NM_003368.4:c.1420+53T= NP_003359.3:n.1420+53T=
NM_003368.5:c.1420+53T= MANE Select NP_003359.3:n.1420+53T=
NM_001017415.2:c.1420+53T= NP_001017415.1:n.1420+53T=
NM_001017416.2:c.1420+53T= NP_001017416.1:n.1420+53T=
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