Canonical Allele Identifier: CA2744232141
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935889dup , CM000663.2:g.77935889dup GRCh38
NC_000001.10:g.78401574dup , CM000663.1:g.78401574dup GRCh37
NC_000001.9:g.78174162dup NCBI36
NG_016625.1:g.52375dup , LRG_442:g.52375dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1318dup MANE Select ENSP00000333938.7:p.Ser440LysfsTer7
ENST00000330010.12:c.1126dup ENSP00000327363.8:p.Ser376LysfsTer7
ENST00000334785.11:c.1318dup ENSP00000333938.7:p.Ser440LysfsTer7
ENST00000342754.5:c.1017dup
ENST00000440324.5:c.1276dup ENSP00000411902.1:p.Ser426LysfsTer7
ENST00000464998.1:n.778dup
ENST00000480732.2:n.892dup
NM_001172309.1:c.1126dup NP_001165780.1:p.Ser376LysfsTer7
NM_144573.3:c.1318dup , LRG_442t1:c.1318dup NP_653174.3:p.Ser440LysfsTer7
XM_005271322.2:c.1318dup XP_005271379.1:p.Ser440LysfsTer7
XM_005271323.2:c.1276dup XP_005271380.1:p.Ser426LysfsTer7
XM_005271324.3:c.1126dup XP_005271381.1:p.Ser376LysfsTer7
XM_005271325.2:c.1251+2410dup XP_005271382.1:n.1251+2410dup
XM_005271326.2:c.1084dup XP_005271383.1:p.Ser362LysfsTer7
XM_005271327.2:c.901dup XP_005271384.1:p.Ser301LysfsTer7
XM_005271322.4:c.1318dup XP_005271379.1:p.Ser440LysfsTer7
XM_005271323.4:c.1276dup XP_005271380.1:p.Ser426LysfsTer7
XM_005271324.5:c.1126dup XP_005271381.1:p.Ser376LysfsTer7
XM_005271325.4:c.1251+2410dup XP_005271382.1:n.1251+2410dup
XM_005271326.4:c.1084dup XP_005271383.1:p.Ser362LysfsTer7
XM_005271327.4:c.901dup XP_005271384.1:p.Ser301LysfsTer7
NM_001172309.2:c.1126dup NP_001165780.1:p.Ser376LysfsTer7
NM_144573.4:c.1318dup MANE Select NP_653174.3:p.Ser440LysfsTer7