Canonical Allele Identifier: CA1171085826
Gene: USP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447497A= , CM000663.2:g.62447497A= GRCh38
NC_000001.10:g.62913168A= , CM000663.1:g.62913168A= GRCh37
NC_000001.9:g.62685756A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1406A= MANE Select ENSP00000343526.4:p.Glu469=
ENST00000339950.4:c.1406A= ENSP00000343526.4:p.Glu469=
ENST00000371146.5:c.1406A= ENSP00000360188.1:p.Glu469=
NM_001017415.1:c.1406A= NP_001017415.1:p.Glu469=
NM_001017416.1:c.1406A= NP_001017416.1:p.Glu469=
NM_003368.4:c.1406A= NP_003359.3:p.Glu469=
NM_003368.5:c.1406A= MANE Select NP_003359.3:p.Glu469=
NM_001017415.2:c.1406A= NP_001017415.1:p.Glu469=
NM_001017416.2:c.1406A= NP_001017416.1:p.Glu469=