Canonical Allele Identifier: CA2574166254
Gene: NEXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942081_77942082del , CM000663.2:g.77942081_77942082del GRCh38
NC_000001.10:g.78407766_78407767del , CM000663.1:g.78407766_78407767del GRCh37
NC_000001.9:g.78180354_78180355del NCBI36
NG_016625.1:g.58567_58568del , LRG_442:g.58567_58568del
NG_033243.2:g.42013_42014del

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1532_1533del MANE Select ENSP00000333938.7:p.Val511GlufsTer5
ENST00000330010.12:c.1340_1341del ENSP00000327363.8:p.Val447GlufsTer5
ENST00000334785.11:c.1532_1533del ENSP00000333938.7:p.Val511GlufsTer5
ENST00000342754.5:c.1231_1232del
ENST00000470735.1:n.371_372del
ENST00000480732.2:n.1106_1107del
NM_001172309.1:c.1340_1341del NP_001165780.1:p.Val447GlufsTer5
NM_144573.3:c.1532_1533del , LRG_442t1:c.1532_1533del NP_653174.3:p.Val511GlufsTer5
XM_005271322.2:c.1532_1533del XP_005271379.1:p.Val511GlufsTer5
XM_005271323.2:c.1490_1491del XP_005271380.1:p.Val497GlufsTer5
XM_005271324.3:c.1340_1341del XP_005271381.1:p.Val447GlufsTer5
XM_005271325.2:c.1310_1311del XP_005271382.1:p.Val437GlufsTer5
XM_005271326.2:c.1298_1299del XP_005271383.1:p.Val433GlufsTer5
XM_005271327.2:c.1115_1116del XP_005271384.1:p.Val372GlufsTer5
XM_005271322.4:c.1532_1533del XP_005271379.1:p.Val511GlufsTer5
XM_005271323.4:c.1490_1491del XP_005271380.1:p.Val497GlufsTer5
XM_005271324.5:c.1340_1341del XP_005271381.1:p.Val447GlufsTer5
XM_005271325.4:c.1310_1311del XP_005271382.1:p.Val437GlufsTer5
XM_005271326.4:c.1298_1299del XP_005271383.1:p.Val433GlufsTer5
XM_005271327.4:c.1115_1116del XP_005271384.1:p.Val372GlufsTer5
NM_001172309.2:c.1340_1341del NP_001165780.1:p.Val447GlufsTer5
NM_144573.4:c.1532_1533del MANE Select NP_653174.3:p.Val511GlufsTer5