Canonical Allele Identifier: CA1002415037

Gene: USP1

Linked Data

• dbSNP Id: rs1645184054
• gnomAD v3: 1-62447532-G-T
• gnomAD v4: 1-62447532-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62447532G>T , CM000663.2:g.62447532G>T	GRCh38
NC_000001.10:g.62913203G>T , CM000663.1:g.62913203G>T	GRCh37
NC_000001.9:g.62685791G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339950.5:c.1420+21G>T MANE Select	ENSP00000343526.4:n.1420+21G>T
ENST00000339950.4:c.1420+21G>T	ENSP00000343526.4:n.1420+21G>T
ENST00000371146.5:c.1420+21G>T	ENSP00000360188.1:n.1420+21G>T
NM_001017415.1:c.1420+21G>T	NP_001017415.1:n.1420+21G>T
NM_001017416.1:c.1420+21G>T	NP_001017416.1:n.1420+21G>T
NM_003368.4:c.1420+21G>T	NP_003359.3:n.1420+21G>T
NM_003368.5:c.1420+21G>T MANE Select	NP_003359.3:n.1420+21G>T
NM_001017415.2:c.1420+21G>T	NP_001017415.1:n.1420+21G>T
NM_001017416.2:c.1420+21G>T	NP_001017416.1:n.1420+21G>T