Canonical Allele Identifier: CA2645983512
Gene: USP1 HGNC NCBI

Linked Data

gnomAD v4: 1-62447598-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447598T>C , CM000663.2:g.62447598T>C GRCh38
NC_000001.10:g.62913269T>C , CM000663.1:g.62913269T>C GRCh37
NC_000001.9:g.62685857T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1420+87T>C MANE Select ENSP00000343526.4:n.1420+87T>C
ENST00000339950.4:c.1420+87T>C ENSP00000343526.4:n.1420+87T>C
ENST00000371146.5:c.1420+87T>C ENSP00000360188.1:n.1420+87T>C
NM_001017415.1:c.1420+87T>C NP_001017415.1:n.1420+87T>C
NM_001017416.1:c.1420+87T>C NP_001017416.1:n.1420+87T>C
NM_003368.4:c.1420+87T>C NP_003359.3:n.1420+87T>C
NM_003368.5:c.1420+87T>C MANE Select NP_003359.3:n.1420+87T>C
NM_001017415.2:c.1420+87T>C NP_001017415.1:n.1420+87T>C
NM_001017416.2:c.1420+87T>C NP_001017416.1:n.1420+87T>C
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