Canonical Allele Identifier: CA1146732793
Gene: USP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447490A= , CM000663.2:g.62447490A= GRCh38
NC_000001.10:g.62913161A= , CM000663.1:g.62913161A= GRCh37
NC_000001.9:g.62685749A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1399A= MANE Select ENSP00000343526.4:p.Lys467=
ENST00000339950.4:c.1399A= ENSP00000343526.4:p.Lys467=
ENST00000371146.5:c.1399A= ENSP00000360188.1:p.Lys467=
NM_001017415.1:c.1399A= NP_001017415.1:p.Lys467=
NM_001017416.1:c.1399A= NP_001017416.1:p.Lys467=
NM_003368.4:c.1399A= NP_003359.3:p.Lys467=
NM_003368.5:c.1399A= MANE Select NP_003359.3:p.Lys467=
NM_001017415.2:c.1399A= NP_001017415.1:p.Lys467=
NM_001017416.2:c.1399A= NP_001017416.1:p.Lys467=