Canonical Allele Identifier: CA1171085829

Gene: USP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447523T= , CM000663.2:g.62447523T=	GRCh38
NC_000001.10:g.62913194T= , CM000663.1:g.62913194T=	GRCh37
NC_000001.9:g.62685782T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+12T= MANE Select	ENSP00000343526.4:n.1420+12T=
ENST00000339950.4:c.1420+12T=	ENSP00000343526.4:n.1420+12T=
ENST00000371146.5:c.1420+12T=	ENSP00000360188.1:n.1420+12T=
NM_001017415.1:c.1420+12T=	NP_001017415.1:n.1420+12T=
NM_001017416.1:c.1420+12T=	NP_001017416.1:n.1420+12T=
NM_003368.4:c.1420+12T=	NP_003359.3:n.1420+12T=
NM_003368.5:c.1420+12T= MANE Select	NP_003359.3:n.1420+12T=
NM_001017415.2:c.1420+12T=	NP_001017415.1:n.1420+12T=
NM_001017416.2:c.1420+12T=	NP_001017416.1:n.1420+12T=