Canonical Allele Identifier: CA2645983163

Gene: USP1

Linked Data

• gnomAD v4: 1-62447240-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447242_62447243del , CM000663.2:g.62447242_62447243del	GRCh38
NC_000001.10:g.62912913_62912914del , CM000663.1:g.62912913_62912914del	GRCh37
NC_000001.9:g.62685501_62685502del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1250-99_1250-98del MANE Select	ENSP00000343526.4:n.1250-99_1250-98del
ENST00000339950.4:c.1250-99_1250-98del	ENSP00000343526.4:n.1250-99_1250-98del
ENST00000371146.5:c.1250-99_1250-98del	ENSP00000360188.1:n.1250-99_1250-98del
NM_001017415.1:c.1250-99_1250-98del	NP_001017415.1:n.1250-99_1250-98del
NM_001017416.1:c.1250-99_1250-98del	NP_001017416.1:n.1250-99_1250-98del
NM_003368.4:c.1250-99_1250-98del	NP_003359.3:n.1250-99_1250-98del
NM_003368.5:c.1250-99_1250-98del MANE Select	NP_003359.3:n.1250-99_1250-98del
NM_001017415.2:c.1250-99_1250-98del	NP_001017415.1:n.1250-99_1250-98del
NM_001017416.2:c.1250-99_1250-98del	NP_001017416.1:n.1250-99_1250-98del