Canonical Allele Identifier: CA340621486

Gene: USP1

Linked Data

• MyVariant Identifiers: chr1:g.62913184T>A (hg19) ; chr1:g.62447513T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447513T>A , CM000663.2:g.62447513T>A	GRCh38
NC_000001.10:g.62913184T>A , CM000663.1:g.62913184T>A	GRCh37
NC_000001.9:g.62685772T>A	NCBI36

Transcript Alleles

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