Canonical Allele Identifier: CA2646274579
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77933556_77933557del , CM000663.2:g.77933556_77933557del GRCh38
NC_000001.10:g.78399241_78399242del , CM000663.1:g.78399241_78399242del GRCh37
NC_000001.9:g.78171829_78171830del NCBI36
NG_016625.1:g.50042_50043del , LRG_442:g.50042_50043del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1251+77_1251+78del MANE Select ENSP00000333938.7:n.1251+77_1251+78del
ENST00000330010.12:c.1059+77_1059+78del ENSP00000327363.8:n.1059+77_1059+78del
ENST00000334785.11:c.1251+77_1251+78del ENSP00000333938.7:n.1251+77_1251+78del
ENST00000342754.5:c.950+77_950+78del
ENST00000440324.5:c.1209+77_1209+78del ENSP00000411902.1:n.1209+77_1209+78del
ENST00000464998.1:n.711+77_711+78del
ENST00000480732.2:n.825+77_825+78del
NM_001172309.1:c.1059+77_1059+78del NP_001165780.1:n.1059+77_1059+78del
NM_144573.3:c.1251+77_1251+78del , LRG_442t1:c.1251+77_1251+78del NP_653174.3:n.1251+77_1251+78del
XM_005271322.2:c.1251+77_1251+78del XP_005271379.1:n.1251+77_1251+78del
XM_005271323.2:c.1209+77_1209+78del XP_005271380.1:n.1209+77_1209+78del
XM_005271324.3:c.1059+77_1059+78del XP_005271381.1:n.1059+77_1059+78del
XM_005271325.2:c.1251+77_1251+78del XP_005271382.1:n.1251+77_1251+78del
XM_005271326.2:c.1017+77_1017+78del XP_005271383.1:n.1017+77_1017+78del
XM_005271327.2:c.834+77_834+78del XP_005271384.1:n.834+77_834+78del
XM_005271322.4:c.1251+77_1251+78del XP_005271379.1:n.1251+77_1251+78del
XM_005271323.4:c.1209+77_1209+78del XP_005271380.1:n.1209+77_1209+78del
XM_005271324.5:c.1059+77_1059+78del XP_005271381.1:n.1059+77_1059+78del
XM_005271325.4:c.1251+77_1251+78del XP_005271382.1:n.1251+77_1251+78del
XM_005271326.4:c.1017+77_1017+78del XP_005271383.1:n.1017+77_1017+78del
XM_005271327.4:c.834+77_834+78del XP_005271384.1:n.834+77_834+78del
NM_001172309.2:c.1059+77_1059+78del NP_001165780.1:n.1059+77_1059+78del
NM_144573.4:c.1251+77_1251+78del MANE Select NP_653174.3:n.1251+77_1251+78del