Canonical Allele Identifier: CA1171085702
Gene: USP1 HGNC NCBI

Linked Data

dbSNP Id: rs778488234

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447146T>G , CM000663.2:g.62447146T>G GRCh38
NC_000001.10:g.62912817T>G , CM000663.1:g.62912817T>G GRCh37
NC_000001.9:g.62685405T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1250-195T>G MANE Select ENSP00000343526.4:n.1250-195T>G
ENST00000339950.4:c.1250-195T>G ENSP00000343526.4:n.1250-195T>G
ENST00000371146.5:c.1250-195T>G ENSP00000360188.1:n.1250-195T>G
NM_001017415.1:c.1250-195T>G NP_001017415.1:n.1250-195T>G
NM_001017416.1:c.1250-195T>G NP_001017416.1:n.1250-195T>G
NM_003368.4:c.1250-195T>G NP_003359.3:n.1250-195T>G
NM_003368.5:c.1250-195T>G MANE Select NP_003359.3:n.1250-195T>G
NM_001017415.2:c.1250-195T>G NP_001017415.1:n.1250-195T>G
NM_001017416.2:c.1250-195T>G NP_001017416.1:n.1250-195T>G