Canonical Allele Identifier: CA23729923

Gene: USP1

Linked Data

• dbSNP Id: rs983228378
• MyVariant Identifiers: chr1:g.62912944A>G (hg19) ; chr1:g.62447273A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447273A>G , CM000663.2:g.62447273A>G	GRCh38
NC_000001.10:g.62912944A>G , CM000663.1:g.62912944A>G	GRCh37
NC_000001.9:g.62685532A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339950.5:c.1250-68A>G MANE Select	ENSP00000343526.4:n.1250-68A>G
ENST00000339950.4:c.1250-68A>G	ENSP00000343526.4:n.1250-68A>G
ENST00000371146.5:c.1250-68A>G	ENSP00000360188.1:n.1250-68A>G
NM_001017415.1:c.1250-68A>G	NP_001017415.1:n.1250-68A>G
NM_001017416.1:c.1250-68A>G	NP_001017416.1:n.1250-68A>G
NM_003368.4:c.1250-68A>G	NP_003359.3:n.1250-68A>G
NM_003368.5:c.1250-68A>G MANE Select	NP_003359.3:n.1250-68A>G
NM_001017415.2:c.1250-68A>G	NP_001017415.1:n.1250-68A>G
NM_001017416.2:c.1250-68A>G	NP_001017416.1:n.1250-68A>G