Canonical Allele Identifier: CA916190932

Gene: USP1

Linked Data

• dbSNP Id: rs1571138192
• gnomAD v3: 1-62447217-TAAG-T
• gnomAD v4: 1-62447217-TAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447218_62447220del , CM000663.2:g.62447218_62447220del	GRCh38
NC_000001.10:g.62912889_62912891del , CM000663.1:g.62912889_62912891del	GRCh37
NC_000001.9:g.62685477_62685479del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1250-123_1250-121del MANE Select	ENSP00000343526.4:n.1250-123_1250-121del
ENST00000339950.4:c.1250-123_1250-121del	ENSP00000343526.4:n.1250-123_1250-121del
ENST00000371146.5:c.1250-123_1250-121del	ENSP00000360188.1:n.1250-123_1250-121del
NM_001017415.1:c.1250-123_1250-121del	NP_001017415.1:n.1250-123_1250-121del
NM_001017416.1:c.1250-123_1250-121del	NP_001017416.1:n.1250-123_1250-121del
NM_003368.4:c.1250-123_1250-121del	NP_003359.3:n.1250-123_1250-121del
NM_003368.5:c.1250-123_1250-121del MANE Select	NP_003359.3:n.1250-123_1250-121del
NM_001017415.2:c.1250-123_1250-121del	NP_001017415.1:n.1250-123_1250-121del
NM_001017416.2:c.1250-123_1250-121del	NP_001017416.1:n.1250-123_1250-121del