Canonical Allele Identifier: CA340620311

Gene: USP1

Linked Data

• MyVariant Identifiers: chr1:g.62913101A>T (hg19) ; chr1:g.62447430A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447430A>T , CM000663.2:g.62447430A>T	GRCh38
NC_000001.10:g.62913101A>T , CM000663.1:g.62913101A>T	GRCh37
NC_000001.9:g.62685689A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1339A>T MANE Select	ENSP00000343526.4:p.Thr447Ser
ENST00000339950.4:c.1339A>T	ENSP00000343526.4:p.Thr447Ser
ENST00000371146.5:c.1339A>T	ENSP00000360188.1:p.Thr447Ser
NM_001017415.1:c.1339A>T	NP_001017415.1:p.Thr447Ser
NM_001017416.1:c.1339A>T	NP_001017416.1:p.Thr447Ser
NM_003368.4:c.1339A>T	NP_003359.3:p.Thr447Ser
NM_003368.5:c.1339A>T MANE Select	NP_003359.3:p.Thr447Ser
NM_001017415.2:c.1339A>T	NP_001017415.1:p.Thr447Ser
NM_001017416.2:c.1339A>T	NP_001017416.1:p.Thr447Ser