Canonical Allele Identifier: CA2645983236

Gene: USP1

Linked Data

• gnomAD v4: 1-62447297-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447299_62447300del , CM000663.2:g.62447299_62447300del	GRCh38
NC_000001.10:g.62912970_62912971del , CM000663.1:g.62912970_62912971del	GRCh37
NC_000001.9:g.62685558_62685559del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1250-42_1250-41del MANE Select	ENSP00000343526.4:n.1250-42_1250-41del
ENST00000339950.4:c.1250-42_1250-41del	ENSP00000343526.4:n.1250-42_1250-41del
ENST00000371146.5:c.1250-42_1250-41del	ENSP00000360188.1:n.1250-42_1250-41del
NM_001017415.1:c.1250-42_1250-41del	NP_001017415.1:n.1250-42_1250-41del
NM_001017416.1:c.1250-42_1250-41del	NP_001017416.1:n.1250-42_1250-41del
NM_003368.4:c.1250-42_1250-41del	NP_003359.3:n.1250-42_1250-41del
NM_003368.5:c.1250-42_1250-41del MANE Select	NP_003359.3:n.1250-42_1250-41del
NM_001017415.2:c.1250-42_1250-41del	NP_001017415.1:n.1250-42_1250-41del
NM_001017416.2:c.1250-42_1250-41del	NP_001017416.1:n.1250-42_1250-41del