Canonical Allele Identifier: CA1177623610
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs1649828437

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77926258_77926259del , CM000663.2:g.77926258_77926259del GRCh38
NC_000001.10:g.78391943_78391944del , CM000663.1:g.78391943_78391944del GRCh37
NC_000001.9:g.78164531_78164532del NCBI36
NG_016625.1:g.42744_42745del , LRG_442:g.42744_42745del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.490-156_490-155del MANE Select ENSP00000333938.7:n.490-156_490-155del
ENST00000330010.12:c.298-156_298-155del ENSP00000327363.8:n.298-156_298-155del
ENST00000334785.11:c.490-156_490-155del ENSP00000333938.7:n.490-156_490-155del
ENST00000342754.5:c.189-156_189-155del
ENST00000401035.7:c.298-156_298-155del ENSP00000383814.3:n.298-156_298-155del
ENST00000440324.5:c.448-156_448-155del ENSP00000411902.1:n.448-156_448-155del
NM_001172309.1:c.298-156_298-155del NP_001165780.1:n.298-156_298-155del
NM_144573.3:c.490-156_490-155del , LRG_442t1:c.490-156_490-155del NP_653174.3:n.490-156_490-155del
XM_005271322.2:c.490-156_490-155del XP_005271379.1:n.490-156_490-155del
XM_005271323.2:c.448-156_448-155del XP_005271380.1:n.448-156_448-155del
XM_005271324.3:c.298-156_298-155del XP_005271381.1:n.298-156_298-155del
XM_005271325.2:c.490-156_490-155del XP_005271382.1:n.490-156_490-155del
XM_005271326.2:c.256-156_256-155del XP_005271383.1:n.256-156_256-155del
XM_005271327.2:c.448-3058_448-3057del XP_005271384.1:n.448-3058_448-3057del
XM_005271322.4:c.490-156_490-155del XP_005271379.1:n.490-156_490-155del
XM_005271323.4:c.448-156_448-155del XP_005271380.1:n.448-156_448-155del
XM_005271324.5:c.298-156_298-155del XP_005271381.1:n.298-156_298-155del
XM_005271325.4:c.490-156_490-155del XP_005271382.1:n.490-156_490-155del
XM_005271326.4:c.256-156_256-155del XP_005271383.1:n.256-156_256-155del
XM_005271327.4:c.448-3058_448-3057del XP_005271384.1:n.448-3058_448-3057del
NM_001172309.2:c.298-156_298-155del NP_001165780.1:n.298-156_298-155del
NM_144573.4:c.490-156_490-155del MANE Select NP_653174.3:n.490-156_490-155del