Canonical Allele Identifier: CA340619676
Gene: USP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.62913044A>C (hg19) chr1:g.62447373A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447373A>C , CM000663.2:g.62447373A>C GRCh38
NC_000001.10:g.62913044A>C , CM000663.1:g.62913044A>C GRCh37
NC_000001.9:g.62685632A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1282A>C MANE Select ENSP00000343526.4:p.Lys428Gln
ENST00000339950.4:c.1282A>C ENSP00000343526.4:p.Lys428Gln
ENST00000371146.5:c.1282A>C ENSP00000360188.1:p.Lys428Gln
NM_001017415.1:c.1282A>C NP_001017415.1:p.Lys428Gln
NM_001017416.1:c.1282A>C NP_001017416.1:p.Lys428Gln
NM_003368.4:c.1282A>C NP_003359.3:p.Lys428Gln
NM_003368.5:c.1282A>C MANE Select NP_003359.3:p.Lys428Gln
NM_001017415.2:c.1282A>C NP_001017415.1:p.Lys428Gln
NM_001017416.2:c.1282A>C NP_001017416.1:p.Lys428Gln
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