Canonical Allele Identifier: CA2645983211
Gene: USP1 HGNC NCBI

Linked Data

gnomAD v4: 1-62447280-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447280T>G , CM000663.2:g.62447280T>G GRCh38
NC_000001.10:g.62912951T>G , CM000663.1:g.62912951T>G GRCh37
NC_000001.9:g.62685539T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339950.5:c.1250-61T>G MANE Select ENSP00000343526.4:n.1250-61T>G
ENST00000339950.4:c.1250-61T>G ENSP00000343526.4:n.1250-61T>G
ENST00000371146.5:c.1250-61T>G ENSP00000360188.1:n.1250-61T>G
NM_001017415.1:c.1250-61T>G NP_001017415.1:n.1250-61T>G
NM_001017416.1:c.1250-61T>G NP_001017416.1:n.1250-61T>G
NM_003368.4:c.1250-61T>G NP_003359.3:n.1250-61T>G
NM_003368.5:c.1250-61T>G MANE Select NP_003359.3:n.1250-61T>G
NM_001017415.2:c.1250-61T>G NP_001017415.1:n.1250-61T>G
NM_001017416.2:c.1250-61T>G NP_001017416.1:n.1250-61T>G