Canonical Allele Identifier: CA2830536988

Gene: USO1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.75757809_75757812del , CM000666.2:g.75757809_75757812del	GRCh38
NC_000004.11:g.76678962_76678965del , CM000666.1:g.76678962_76678965del	GRCh37
NC_000004.10:g.76897986_76897989del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000514213.7:c.295+236_295+239del MANE Select	ENSP00000444850.2:n.295+236_295+239del
ENST00000264904.8:c.295+236_295+239del	ENSP00000264904.7:n.295+236_295+239del
ENST00000514213.6:c.295+236_295+239del	ENSP00000444850.2:n.295+236_295+239del
NM_001290049.1:c.295+236_295+239del	NP_001276978.1:n.295+236_295+239del
NM_003715.3:c.295+236_295+239del	NP_003706.2:n.295+236_295+239del
XM_006714396.2:c.295+236_295+239del	XP_006714459.1:n.295+236_295+239del
XM_006714397.2:c.295+236_295+239del	XP_006714460.1:n.295+236_295+239del
XM_006714396.4:c.295+236_295+239del	XP_006714459.1:n.295+236_295+239del
XM_006714397.3:c.295+236_295+239del	XP_006714460.1:n.295+236_295+239del
NM_001290049.2:c.295+236_295+239del	NP_001276978.1:n.295+236_295+239del
NM_003715.4:c.295+236_295+239del MANE Select	NP_003706.2:n.295+236_295+239del