Canonical Allele Identifier: CA2645983418

Gene: USP1

Linked Data

• gnomAD v4: 1-62447532-G-C

Genomic Alleles

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

Transcript Alleles

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