Canonical Allele Identifier: CA340619586
Gene: USP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.62913030T>A (hg19) chr1:g.62447359T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447359T>A , CM000663.2:g.62447359T>A GRCh38
NC_000001.10:g.62913030T>A , CM000663.1:g.62913030T>A GRCh37
NC_000001.9:g.62685618T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1268T>A MANE Select ENSP00000343526.4:p.Phe423Tyr
ENST00000339950.4:c.1268T>A ENSP00000343526.4:p.Phe423Tyr
ENST00000371146.5:c.1268T>A ENSP00000360188.1:p.Phe423Tyr
NM_001017415.1:c.1268T>A NP_001017415.1:p.Phe423Tyr
NM_001017416.1:c.1268T>A NP_001017416.1:p.Phe423Tyr
NM_003368.4:c.1268T>A NP_003359.3:p.Phe423Tyr
NM_003368.5:c.1268T>A MANE Select NP_003359.3:p.Phe423Tyr
NM_001017415.2:c.1268T>A NP_001017415.1:p.Phe423Tyr
NM_001017416.2:c.1268T>A NP_001017416.1:p.Phe423Tyr
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