Canonical Allele Identifier: CA1171085853

Gene: USP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447576_62447577delinsGT , CM000663.2:g.62447576_62447577delinsGT	GRCh38
NC_000001.10:g.62913247_62913248delinsGT , CM000663.1:g.62913247_62913248delinsGT	GRCh37
NC_000001.9:g.62685835_62685836delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+65_1420+66delinsGT MANE Select	ENSP00000343526.4:n.1420+65_1420+66delinsGT
ENST00000339950.4:c.1420+65_1420+66delinsGT	ENSP00000343526.4:n.1420+65_1420+66delinsGT
ENST00000371146.5:c.1420+65_1420+66delinsGT	ENSP00000360188.1:n.1420+65_1420+66delinsGT
NM_001017415.1:c.1420+65_1420+66delinsGT	NP_001017415.1:n.1420+65_1420+66delinsGT
NM_001017416.1:c.1420+65_1420+66delinsGT	NP_001017416.1:n.1420+65_1420+66delinsGT
NM_003368.4:c.1420+65_1420+66delinsGT	NP_003359.3:n.1420+65_1420+66delinsGT
NM_003368.5:c.1420+65_1420+66delinsGT MANE Select	NP_003359.3:n.1420+65_1420+66delinsGT
NM_001017415.2:c.1420+65_1420+66delinsGT	NP_001017415.1:n.1420+65_1420+66delinsGT
NM_001017416.2:c.1420+65_1420+66delinsGT	NP_001017416.1:n.1420+65_1420+66delinsGT