Canonical Allele Identifier: CA1171085849

Gene: USP1

Linked Data

• dbSNP Id: rs1645184305

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447566_62447567insACTTTCA , CM000663.2:g.62447566_62447567insACTTTCA	GRCh38
NC_000001.10:g.62913237_62913238insACTTTCA , CM000663.1:g.62913237_62913238insACTTTCA	GRCh37
NC_000001.9:g.62685825_62685826insACTTTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+55_1420+56insACTTTCA MANE Select	ENSP00000343526.4:n.1420+55_1420+56insACTTTCA
ENST00000339950.4:c.1420+55_1420+56insACTTTCA	ENSP00000343526.4:n.1420+55_1420+56insACTTTCA
ENST00000371146.5:c.1420+55_1420+56insACTTTCA	ENSP00000360188.1:n.1420+55_1420+56insACTTTCA
NM_001017415.1:c.1420+55_1420+56insACTTTCA	NP_001017415.1:n.1420+55_1420+56insACTTTCA
NM_001017416.1:c.1420+55_1420+56insACTTTCA	NP_001017416.1:n.1420+55_1420+56insACTTTCA
NM_003368.4:c.1420+55_1420+56insACTTTCA	NP_003359.3:n.1420+55_1420+56insACTTTCA
NM_003368.5:c.1420+55_1420+56insACTTTCA MANE Select	NP_003359.3:n.1420+55_1420+56insACTTTCA
NM_001017415.2:c.1420+55_1420+56insACTTTCA	NP_001017415.1:n.1420+55_1420+56insACTTTCA
NM_001017416.2:c.1420+55_1420+56insACTTTCA	NP_001017416.1:n.1420+55_1420+56insACTTTCA