Canonical Allele Identifier: CA2574414089
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77933368_77933371del , CM000663.2:g.77933368_77933371del GRCh38
NC_000001.10:g.78399053_78399056del , CM000663.1:g.78399053_78399056del GRCh37
NC_000001.9:g.78171641_78171644del NCBI36
NG_016625.1:g.49854_49857del , LRG_442:g.49854_49857del

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1140_1143del MANE Select ENSP00000333938.7:p.Glu380AspfsTer2
ENST00000330010.12:c.948_951del ENSP00000327363.8:p.Glu316AspfsTer2
ENST00000334785.11:c.1140_1143del ENSP00000333938.7:p.Glu380AspfsTer2
ENST00000342754.5:c.839_842del
ENST00000401035.7:c.948_951del ENSP00000383814.3:p.Glu316AspfsTer2
ENST00000440324.5:c.1098_1101del ENSP00000411902.1:p.Glu366AspfsTer2
ENST00000464998.1:n.600_603del
ENST00000480732.2:n.714_717del
NM_001172309.1:c.948_951del NP_001165780.1:p.Glu316AspfsTer2
NM_144573.3:c.1140_1143del , LRG_442t1:c.1140_1143del NP_653174.3:p.Glu380AspfsTer2
XM_005271322.2:c.1140_1143del XP_005271379.1:p.Glu380AspfsTer2
XM_005271323.2:c.1098_1101del XP_005271380.1:p.Glu366AspfsTer2
XM_005271324.3:c.948_951del XP_005271381.1:p.Glu316AspfsTer2
XM_005271325.2:c.1140_1143del XP_005271382.1:p.Glu380AspfsTer2
XM_005271326.2:c.906_909del XP_005271383.1:p.Glu302AspfsTer2
XM_005271327.2:c.723_726del XP_005271384.1:p.Glu241AspfsTer2
XM_005271322.4:c.1140_1143del XP_005271379.1:p.Glu380AspfsTer2
XM_005271323.4:c.1098_1101del XP_005271380.1:p.Glu366AspfsTer2
XM_005271324.5:c.948_951del XP_005271381.1:p.Glu316AspfsTer2
XM_005271325.4:c.1140_1143del XP_005271382.1:p.Glu380AspfsTer2
XM_005271326.4:c.906_909del XP_005271383.1:p.Glu302AspfsTer2
XM_005271327.4:c.723_726del XP_005271384.1:p.Glu241AspfsTer2
NM_001172309.2:c.948_951del NP_001165780.1:p.Glu316AspfsTer2
NM_144573.4:c.1140_1143del MANE Select NP_653174.3:p.Glu380AspfsTer2