Canonical Allele Identifier: CA1002414938
Gene: USP1 HGNC NCBI

Linked Data

dbSNP Id: rs1645180493
gnomAD v3: 1-62447051-G-C
gnomAD v4: 1-62447051-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447051G>C , CM000663.2:g.62447051G>C GRCh38
NC_000001.10:g.62912722G>C , CM000663.1:g.62912722G>C GRCh37
NC_000001.9:g.62685310G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1250-290G>C MANE Select ENSP00000343526.4:n.1250-290G>C
ENST00000339950.4:c.1250-290G>C ENSP00000343526.4:n.1250-290G>C
ENST00000371146.5:c.1250-290G>C ENSP00000360188.1:n.1250-290G>C
NM_001017415.1:c.1250-290G>C NP_001017415.1:n.1250-290G>C
NM_001017416.1:c.1250-290G>C NP_001017416.1:n.1250-290G>C
NM_003368.4:c.1250-290G>C NP_003359.3:n.1250-290G>C
NM_003368.5:c.1250-290G>C MANE Select NP_003359.3:n.1250-290G>C
NM_001017415.2:c.1250-290G>C NP_001017415.1:n.1250-290G>C
NM_001017416.2:c.1250-290G>C NP_001017416.1:n.1250-290G>C