Canonical Allele Identifier: CA2646274521
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77933378_77933382del , CM000663.2:g.77933378_77933382del GRCh38
NC_000001.10:g.78399063_78399067del , CM000663.1:g.78399063_78399067del GRCh37
NC_000001.9:g.78171651_78171655del NCBI36
NG_016625.1:g.49864_49868del , LRG_442:g.49864_49868del

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.1150_1154del MANE Select ENSP00000333938.7:p.Gln384AsnfsTer15
ENST00000330010.12:c.958_962del ENSP00000327363.8:p.Gln320AsnfsTer15
ENST00000334785.11:c.1150_1154del ENSP00000333938.7:p.Gln384AsnfsTer15
ENST00000342754.5:c.849_853del
ENST00000401035.7:c.958_962del ENSP00000383814.3:p.Gln320=
ENST00000440324.5:c.1108_1112del ENSP00000411902.1:p.Gln370AsnfsTer15
ENST00000464998.1:n.610_614del
ENST00000480732.2:n.724_728del
NM_001172309.1:c.958_962del NP_001165780.1:p.Gln320AsnfsTer15
NM_144573.3:c.1150_1154del , LRG_442t1:c.1150_1154del NP_653174.3:p.Gln384AsnfsTer15
XM_005271322.2:c.1150_1154del XP_005271379.1:p.Gln384AsnfsTer15
XM_005271323.2:c.1108_1112del XP_005271380.1:p.Gln370AsnfsTer15
XM_005271324.3:c.958_962del XP_005271381.1:p.Gln320AsnfsTer15
XM_005271325.2:c.1150_1154del XP_005271382.1:p.Gln384AsnfsTer15
XM_005271326.2:c.916_920del XP_005271383.1:p.Gln306AsnfsTer15
XM_005271327.2:c.733_737del XP_005271384.1:p.Gln245AsnfsTer15
XM_005271322.4:c.1150_1154del XP_005271379.1:p.Gln384AsnfsTer15
XM_005271323.4:c.1108_1112del XP_005271380.1:p.Gln370AsnfsTer15
XM_005271324.5:c.958_962del XP_005271381.1:p.Gln320AsnfsTer15
XM_005271325.4:c.1150_1154del XP_005271382.1:p.Gln384AsnfsTer15
XM_005271326.4:c.916_920del XP_005271383.1:p.Gln306AsnfsTer15
XM_005271327.4:c.733_737del XP_005271384.1:p.Gln245AsnfsTer15
NM_001172309.2:c.958_962del NP_001165780.1:p.Gln320AsnfsTer15
NM_144573.4:c.1150_1154del MANE Select NP_653174.3:p.Gln384AsnfsTer15