Canonical Allele Identifier: CA2646274715
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935961del , CM000663.2:g.77935961del GRCh38
NC_000001.10:g.78401646del , CM000663.1:g.78401646del GRCh37
NC_000001.9:g.78174234del NCBI36
NG_016625.1:g.52447del , LRG_442:g.52447del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1390del MANE Select ENSP00000333938.7:p.Gln464ArgfsTer4
ENST00000330010.12:c.1198del ENSP00000327363.8:p.Gln400ArgfsTer4
ENST00000334785.11:c.1390del ENSP00000333938.7:p.Gln464ArgfsTer4
ENST00000342754.5:c.1089del
ENST00000464998.1:n.850del
ENST00000480732.2:n.964del
NM_001172309.1:c.1198del NP_001165780.1:p.Gln400ArgfsTer4
NM_144573.3:c.1390del , LRG_442t1:c.1390del NP_653174.3:p.Gln464ArgfsTer4
XM_005271322.2:c.1390del XP_005271379.1:p.Gln464ArgfsTer4
XM_005271323.2:c.1348del XP_005271380.1:p.Gln450ArgfsTer4
XM_005271324.3:c.1198del XP_005271381.1:p.Gln400ArgfsTer4
XM_005271325.2:c.1251+2482del XP_005271382.1:n.1251+2482del
XM_005271326.2:c.1156del XP_005271383.1:p.Gln386ArgfsTer4
XM_005271327.2:c.973del XP_005271384.1:p.Gln325ArgfsTer4
XM_005271322.4:c.1390del XP_005271379.1:p.Gln464ArgfsTer4
XM_005271323.4:c.1348del XP_005271380.1:p.Gln450ArgfsTer4
XM_005271324.5:c.1198del XP_005271381.1:p.Gln400ArgfsTer4
XM_005271325.4:c.1251+2482del XP_005271382.1:n.1251+2482del
XM_005271326.4:c.1156del XP_005271383.1:p.Gln386ArgfsTer4
XM_005271327.4:c.973del XP_005271384.1:p.Gln325ArgfsTer4
NM_001172309.2:c.1198del NP_001165780.1:p.Gln400ArgfsTer4
NM_144573.4:c.1390del MANE Select NP_653174.3:p.Gln464ArgfsTer4