Canonical Allele Identifier: CA1171085824

Gene: USP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447491A= , CM000663.2:g.62447491A=	GRCh38
NC_000001.10:g.62913162A= , CM000663.1:g.62913162A=	GRCh37
NC_000001.9:g.62685750A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1400A= MANE Select	ENSP00000343526.4:p.Lys467=
ENST00000339950.4:c.1400A=	ENSP00000343526.4:p.Lys467=
ENST00000371146.5:c.1400A=	ENSP00000360188.1:p.Lys467=
NM_001017415.1:c.1400A=	NP_001017415.1:p.Lys467=
NM_001017416.1:c.1400A=	NP_001017416.1:p.Lys467=
NM_003368.4:c.1400A=	NP_003359.3:p.Lys467=
NM_003368.5:c.1400A= MANE Select	NP_003359.3:p.Lys467=
NM_001017415.2:c.1400A=	NP_001017415.1:p.Lys467=
NM_001017416.2:c.1400A=	NP_001017416.1:p.Lys467=