Canonical Allele Identifier: CA418002155

Gene: USP1

Linked Data

• dbSNP Id: rs1260619018
• MyVariant Identifiers: chr1:g.62912978_62912979del (hg19) ; chr1:g.62447307_62447308del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447308_62447309del , CM000663.2:g.62447308_62447309del	GRCh38
NC_000001.10:g.62912979_62912980del , CM000663.1:g.62912979_62912980del	GRCh37
NC_000001.9:g.62685567_62685568del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1250-33_1250-32del MANE Select	ENSP00000343526.4:n.1250-33_1250-32del
ENST00000339950.4:c.1250-33_1250-32del	ENSP00000343526.4:n.1250-33_1250-32del
ENST00000371146.5:c.1250-33_1250-32del	ENSP00000360188.1:n.1250-33_1250-32del
NM_001017415.1:c.1250-33_1250-32del	NP_001017415.1:n.1250-33_1250-32del
NM_001017416.1:c.1250-33_1250-32del	NP_001017416.1:n.1250-33_1250-32del
NM_003368.4:c.1250-33_1250-32del	NP_003359.3:n.1250-33_1250-32del
NM_003368.5:c.1250-33_1250-32del MANE Select	NP_003359.3:n.1250-33_1250-32del
NM_001017415.2:c.1250-33_1250-32del	NP_001017415.1:n.1250-33_1250-32del
NM_001017416.2:c.1250-33_1250-32del	NP_001017416.1:n.1250-33_1250-32del