Canonical Allele Identifier: CA340621280
Gene: USP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.62913170G>C (hg19) chr1:g.62447499G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62447499G>C , CM000663.2:g.62447499G>C GRCh38
NC_000001.10:g.62913170G>C , CM000663.1:g.62913170G>C GRCh37
NC_000001.9:g.62685758G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339950.5:c.1408G>C MANE Select ENSP00000343526.4:p.Glu470Gln
ENST00000339950.4:c.1408G>C ENSP00000343526.4:p.Glu470Gln
ENST00000371146.5:c.1408G>C ENSP00000360188.1:p.Glu470Gln
NM_001017415.1:c.1408G>C NP_001017415.1:p.Glu470Gln
NM_001017416.1:c.1408G>C NP_001017416.1:p.Glu470Gln
NM_003368.4:c.1408G>C NP_003359.3:p.Glu470Gln
NM_003368.5:c.1408G>C MANE Select NP_003359.3:p.Glu470Gln
NM_001017415.2:c.1408G>C NP_001017415.1:p.Glu470Gln
NM_001017416.2:c.1408G>C NP_001017416.1:p.Glu470Gln
Search 100 bp 5'
Search 100 bp 3'