Canonical Allele Identifier: CA418002279
Gene: USP1 HGNC NCBI

Linked Data

gnomAD v4: 1-62447498-G-A
MyVariant Identifiers: chr1:g.62913169G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447498G>A , CM000663.2:g.62447498G>A GRCh38
NC_000001.10:g.62913169G>A , CM000663.1:g.62913169G>A GRCh37
NC_000001.9:g.62685757G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1407G>A MANE Select ENSP00000343526.4:p.Glu469=
ENST00000339950.4:c.1407G>A ENSP00000343526.4:p.Glu469=
ENST00000371146.5:c.1407G>A ENSP00000360188.1:p.Glu469=
NM_001017415.1:c.1407G>A NP_001017415.1:p.Glu469=
NM_001017416.1:c.1407G>A NP_001017416.1:p.Glu469=
NM_003368.4:c.1407G>A NP_003359.3:p.Glu469=
NM_003368.5:c.1407G>A MANE Select NP_003359.3:p.Glu469=
NM_001017415.2:c.1407G>A NP_001017415.1:p.Glu469=
NM_001017416.2:c.1407G>A NP_001017416.1:p.Glu469=
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