Canonical Allele Identifier: CA1171085831

Gene: USP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447529C= , CM000663.2:g.62447529C=	GRCh38
NC_000001.10:g.62913200C= , CM000663.1:g.62913200C=	GRCh37
NC_000001.9:g.62685788C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+18C= MANE Select	ENSP00000343526.4:n.1420+18C=
ENST00000339950.4:c.1420+18C=	ENSP00000343526.4:n.1420+18C=
ENST00000371146.5:c.1420+18C=	ENSP00000360188.1:n.1420+18C=
NM_001017415.1:c.1420+18C=	NP_001017415.1:n.1420+18C=
NM_001017416.1:c.1420+18C=	NP_001017416.1:n.1420+18C=
NM_003368.4:c.1420+18C=	NP_003359.3:n.1420+18C=
NM_003368.5:c.1420+18C= MANE Select	NP_003359.3:n.1420+18C=
NM_001017415.2:c.1420+18C=	NP_001017415.1:n.1420+18C=
NM_001017416.2:c.1420+18C=	NP_001017416.1:n.1420+18C=