Canonical Allele Identifier: CA2646274713
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77935868del , CM000663.2:g.77935868del GRCh38
NC_000001.10:g.78401553del , CM000663.1:g.78401553del GRCh37
NC_000001.9:g.78174141del NCBI36
NG_016625.1:g.52354del , LRG_442:g.52354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.1297del MANE Select ENSP00000333938.7:p.Glu433AsnfsTer2
ENST00000330010.12:c.1105del ENSP00000327363.8:p.Glu369AsnfsTer2
ENST00000334785.11:c.1297del ENSP00000333938.7:p.Glu433AsnfsTer2
ENST00000342754.5:c.996del
ENST00000440324.5:c.1255del ENSP00000411902.1:p.Glu419AsnfsTer2
ENST00000464998.1:n.757del
ENST00000480732.2:n.871del
NM_001172309.1:c.1105del NP_001165780.1:p.Glu369AsnfsTer2
NM_144573.3:c.1297del , LRG_442t1:c.1297del NP_653174.3:p.Glu433AsnfsTer2
XM_005271322.2:c.1297del XP_005271379.1:p.Glu433AsnfsTer2
XM_005271323.2:c.1255del XP_005271380.1:p.Glu419AsnfsTer2
XM_005271324.3:c.1105del XP_005271381.1:p.Glu369AsnfsTer2
XM_005271325.2:c.1251+2389del XP_005271382.1:n.1251+2389del
XM_005271326.2:c.1063del XP_005271383.1:p.Glu355AsnfsTer2
XM_005271327.2:c.880del XP_005271384.1:p.Glu294AsnfsTer2
XM_005271322.4:c.1297del XP_005271379.1:p.Glu433AsnfsTer2
XM_005271323.4:c.1255del XP_005271380.1:p.Glu419AsnfsTer2
XM_005271324.5:c.1105del XP_005271381.1:p.Glu369AsnfsTer2
XM_005271325.4:c.1251+2389del XP_005271382.1:n.1251+2389del
XM_005271326.4:c.1063del XP_005271383.1:p.Glu355AsnfsTer2
XM_005271327.4:c.880del XP_005271384.1:p.Glu294AsnfsTer2
NM_001172309.2:c.1105del NP_001165780.1:p.Glu369AsnfsTer2
NM_144573.4:c.1297del MANE Select NP_653174.3:p.Glu433AsnfsTer2