Canonical Allele Identifier: CA2696111130

Gene: USP1

Linked Data

• dbSNP Id: rs2149207267

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447535_62447536dup , CM000663.2:g.62447535_62447536dup	GRCh38
NC_000001.10:g.62913206_62913207dup , CM000663.1:g.62913206_62913207dup	GRCh37
NC_000001.9:g.62685794_62685795dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+24_1420+25dup MANE Select	ENSP00000343526.4:n.1420+24_1420+25dup
ENST00000339950.4:c.1420+24_1420+25dup	ENSP00000343526.4:n.1420+24_1420+25dup
ENST00000371146.5:c.1420+24_1420+25dup	ENSP00000360188.1:n.1420+24_1420+25dup
NM_001017415.1:c.1420+24_1420+25dup	NP_001017415.1:n.1420+24_1420+25dup
NM_001017416.1:c.1420+24_1420+25dup	NP_001017416.1:n.1420+24_1420+25dup
NM_003368.4:c.1420+24_1420+25dup	NP_003359.3:n.1420+24_1420+25dup
NM_003368.5:c.1420+24_1420+25dup MANE Select	NP_003359.3:n.1420+24_1420+25dup
NM_001017415.2:c.1420+24_1420+25dup	NP_001017415.1:n.1420+24_1420+25dup
NM_001017416.2:c.1420+24_1420+25dup	NP_001017416.1:n.1420+24_1420+25dup