Canonical Allele Identifier: CA1003482891
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs1650710022

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935832del , CM000663.2:g.77935832del GRCh38
NC_000001.10:g.78401517del , CM000663.1:g.78401517del GRCh37
NC_000001.9:g.78174105del NCBI36
NG_016625.1:g.52318del , LRG_442:g.52318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1261del MANE Select ENSP00000333938.7:p.Glu421LysfsTer7
ENST00000330010.12:c.1069del ENSP00000327363.8:p.Glu357LysfsTer7
ENST00000334785.11:c.1261del ENSP00000333938.7:p.Glu421LysfsTer7
ENST00000342754.5:c.960del
ENST00000440324.5:c.1219del ENSP00000411902.1:p.Glu407LysfsTer7
ENST00000464998.1:n.721del
ENST00000480732.2:n.835del
NM_001172309.1:c.1069del NP_001165780.1:p.Glu357LysfsTer7
NM_144573.3:c.1261del , LRG_442t1:c.1261del NP_653174.3:p.Glu421LysfsTer7
XM_005271322.2:c.1261del XP_005271379.1:p.Glu421LysfsTer7
XM_005271323.2:c.1219del XP_005271380.1:p.Glu407LysfsTer7
XM_005271324.3:c.1069del XP_005271381.1:p.Glu357LysfsTer7
XM_005271325.2:c.1251+2353del XP_005271382.1:n.1251+2353del
XM_005271326.2:c.1027del XP_005271383.1:p.Glu343LysfsTer7
XM_005271327.2:c.844del XP_005271384.1:p.Glu282LysfsTer7
XM_005271322.4:c.1261del XP_005271379.1:p.Glu421LysfsTer7
XM_005271323.4:c.1219del XP_005271380.1:p.Glu407LysfsTer7
XM_005271324.5:c.1069del XP_005271381.1:p.Glu357LysfsTer7
XM_005271325.4:c.1251+2353del XP_005271382.1:n.1251+2353del
XM_005271326.4:c.1027del XP_005271383.1:p.Glu343LysfsTer7
XM_005271327.4:c.844del XP_005271384.1:p.Glu282LysfsTer7
NM_001172309.2:c.1069del NP_001165780.1:p.Glu357LysfsTer7
NM_144573.4:c.1261del MANE Select NP_653174.3:p.Glu421LysfsTer7