Canonical Allele Identifier: CA2645983478

Gene: USP1

Linked Data

• gnomAD v4: 1-62447577-TTTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447579_62447582del , CM000663.2:g.62447579_62447582del	GRCh38
NC_000001.10:g.62913250_62913253del , CM000663.1:g.62913250_62913253del	GRCh37
NC_000001.9:g.62685838_62685841del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+68_1420+71del MANE Select	ENSP00000343526.4:n.1420+68_1420+71del
ENST00000339950.4:c.1420+68_1420+71del	ENSP00000343526.4:n.1420+68_1420+71del
ENST00000371146.5:c.1420+68_1420+71del	ENSP00000360188.1:n.1420+68_1420+71del
NM_001017415.1:c.1420+68_1420+71del	NP_001017415.1:n.1420+68_1420+71del
NM_001017416.1:c.1420+68_1420+71del	NP_001017416.1:n.1420+68_1420+71del
NM_003368.4:c.1420+68_1420+71del	NP_003359.3:n.1420+68_1420+71del
NM_003368.5:c.1420+68_1420+71del MANE Select	NP_003359.3:n.1420+68_1420+71del
NM_001017415.2:c.1420+68_1420+71del	NP_001017415.1:n.1420+68_1420+71del
NM_001017416.2:c.1420+68_1420+71del	NP_001017416.1:n.1420+68_1420+71del