Canonical Allele Identifier: CA1140183526
Gene: USP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447248C= , CM000663.2:g.62447248C= GRCh38
NC_000001.10:g.62912919C= , CM000663.1:g.62912919C= GRCh37
NC_000001.9:g.62685507C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339950.5:c.1250-93C= MANE Select ENSP00000343526.4:n.1250-93C=
ENST00000339950.4:c.1250-93C= ENSP00000343526.4:n.1250-93C=
ENST00000371146.5:c.1250-93C= ENSP00000360188.1:n.1250-93C=
NM_001017415.1:c.1250-93C= NP_001017415.1:n.1250-93C=
NM_001017416.1:c.1250-93C= NP_001017416.1:n.1250-93C=
NM_003368.4:c.1250-93C= NP_003359.3:n.1250-93C=
NM_003368.5:c.1250-93C= MANE Select NP_003359.3:n.1250-93C=
NM_001017415.2:c.1250-93C= NP_001017415.1:n.1250-93C=
NM_001017416.2:c.1250-93C= NP_001017416.1:n.1250-93C=