Canonical Allele Identifier: CA737669216

Gene: USP1

Linked Data

• dbSNP Id: rs1342662580
• gnomAD v4: 1-62447600-G-C
• MyVariant Identifiers: chr1:g.62913271G>C (hg19) ; chr1:g.62447600G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447600G>C , CM000663.2:g.62447600G>C	GRCh38
NC_000001.10:g.62913271G>C , CM000663.1:g.62913271G>C	GRCh37
NC_000001.9:g.62685859G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+89G>C MANE Select	ENSP00000343526.4:n.1420+89G>C
ENST00000339950.4:c.1420+89G>C	ENSP00000343526.4:n.1420+89G>C
ENST00000371146.5:c.1420+89G>C	ENSP00000360188.1:n.1420+89G>C
NM_001017415.1:c.1420+89G>C	NP_001017415.1:n.1420+89G>C
NM_001017416.1:c.1420+89G>C	NP_001017416.1:n.1420+89G>C
NM_003368.4:c.1420+89G>C	NP_003359.3:n.1420+89G>C
NM_003368.5:c.1420+89G>C MANE Select	NP_003359.3:n.1420+89G>C
NM_001017415.2:c.1420+89G>C	NP_001017415.1:n.1420+89G>C
NM_001017416.2:c.1420+89G>C	NP_001017416.1:n.1420+89G>C