Canonical Allele Identifier: CA1002414989
Gene: USP1 HGNC NCBI

Linked Data

dbSNP Id: rs1645182206
gnomAD v3: 1-62447257-C-G
gnomAD v4: 1-62447257-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447257C>G , CM000663.2:g.62447257C>G GRCh38
NC_000001.10:g.62912928C>G , CM000663.1:g.62912928C>G GRCh37
NC_000001.9:g.62685516C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339950.5:c.1250-84C>G MANE Select ENSP00000343526.4:n.1250-84C>G
ENST00000339950.4:c.1250-84C>G ENSP00000343526.4:n.1250-84C>G
ENST00000371146.5:c.1250-84C>G ENSP00000360188.1:n.1250-84C>G
NM_001017415.1:c.1250-84C>G NP_001017415.1:n.1250-84C>G
NM_001017416.1:c.1250-84C>G NP_001017416.1:n.1250-84C>G
NM_003368.4:c.1250-84C>G NP_003359.3:n.1250-84C>G
NM_003368.5:c.1250-84C>G MANE Select NP_003359.3:n.1250-84C>G
NM_001017415.2:c.1250-84C>G NP_001017415.1:n.1250-84C>G
NM_001017416.2:c.1250-84C>G NP_001017416.1:n.1250-84C>G