Canonical Allele Identifier: CA2646274567
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77933547_77933574del , CM000663.2:g.77933547_77933574del GRCh38
NC_000001.10:g.78399232_78399259del , CM000663.1:g.78399232_78399259del GRCh37
NC_000001.9:g.78171820_78171847del NCBI36
NG_016625.1:g.50033_50060del , LRG_442:g.50033_50060del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1251+68_1251+95del MANE Select ENSP00000333938.7:n.1251+68_1251+95del
ENST00000330010.12:c.1059+68_1059+95del ENSP00000327363.8:n.1059+68_1059+95del
ENST00000334785.11:c.1251+68_1251+95del ENSP00000333938.7:n.1251+68_1251+95del
ENST00000342754.5:c.950+68_950+95del
ENST00000440324.5:c.1209+68_1209+95del ENSP00000411902.1:n.1209+68_1209+95del
ENST00000464998.1:n.711+68_711+95del
ENST00000480732.2:n.825+68_825+95del
NM_001172309.1:c.1059+68_1059+95del NP_001165780.1:n.1059+68_1059+95del
NM_144573.3:c.1251+68_1251+95del , LRG_442t1:c.1251+68_1251+95del NP_653174.3:n.1251+68_1251+95del
XM_005271322.2:c.1251+68_1251+95del XP_005271379.1:n.1251+68_1251+95del
XM_005271323.2:c.1209+68_1209+95del XP_005271380.1:n.1209+68_1209+95del
XM_005271324.3:c.1059+68_1059+95del XP_005271381.1:n.1059+68_1059+95del
XM_005271325.2:c.1251+68_1251+95del XP_005271382.1:n.1251+68_1251+95del
XM_005271326.2:c.1017+68_1017+95del XP_005271383.1:n.1017+68_1017+95del
XM_005271327.2:c.834+68_834+95del XP_005271384.1:n.834+68_834+95del
XM_005271322.4:c.1251+68_1251+95del XP_005271379.1:n.1251+68_1251+95del
XM_005271323.4:c.1209+68_1209+95del XP_005271380.1:n.1209+68_1209+95del
XM_005271324.5:c.1059+68_1059+95del XP_005271381.1:n.1059+68_1059+95del
XM_005271325.4:c.1251+68_1251+95del XP_005271382.1:n.1251+68_1251+95del
XM_005271326.4:c.1017+68_1017+95del XP_005271383.1:n.1017+68_1017+95del
XM_005271327.4:c.834+68_834+95del XP_005271384.1:n.834+68_834+95del
NM_001172309.2:c.1059+68_1059+95del NP_001165780.1:n.1059+68_1059+95del
NM_144573.4:c.1251+68_1251+95del MANE Select NP_653174.3:n.1251+68_1251+95del