Canonical Allele Identifier: CA2646275803
Gene: NEXN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942910_77942912del , CM000663.2:g.77942910_77942912del GRCh38
NC_000001.10:g.78408595_78408597del , CM000663.1:g.78408595_78408597del GRCh37
NC_000001.9:g.78181183_78181185del NCBI36
NG_016625.1:g.59396_59398del , LRG_442:g.59396_59398del
NG_033243.2:g.41186_41188del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.*81_*83del MANE Select ENSP00000333938.7:n.*81_*83del
ENST00000330010.12:c.*81_*83del ENSP00000327363.8:n.*81_*83del
ENST00000334785.11:c.*81_*83del ENSP00000333938.7:n.*81_*83del
ENST00000342754.5:c.1727_1729del
ENST00000480732.2:n.1683_1685del
NM_001172309.1:c.*81_*83del NP_001165780.1:n.*81_*83del
NM_144573.3:c.*81_*83del , LRG_442t1:c.*81_*83del NP_653174.3:n.*81_*83del
XM_005271322.2:c.2028_2030del XP_005271379.1:p.Tyr676Ter
XM_005271323.2:c.1986_1988del XP_005271380.1:p.Tyr662Ter
XM_005271324.3:c.1836_1838del XP_005271381.1:p.Tyr612Ter
XM_005271325.2:c.1806_1808del XP_005271382.1:p.Tyr602Ter
XM_005271326.2:c.1794_1796del XP_005271383.1:p.Tyr598Ter
XM_005271327.2:c.1611_1613del XP_005271384.1:p.Tyr537Ter
XM_005271322.4:c.2028_2030del XP_005271379.1:p.Tyr676Ter
XM_005271323.4:c.1986_1988del XP_005271380.1:p.Tyr662Ter
XM_005271324.5:c.1836_1838del XP_005271381.1:p.Tyr612Ter
XM_005271325.4:c.1806_1808del XP_005271382.1:p.Tyr602Ter
XM_005271326.4:c.1794_1796del XP_005271383.1:p.Tyr598Ter
XM_005271327.4:c.1611_1613del XP_005271384.1:p.Tyr537Ter
NM_001172309.2:c.*81_*83del NP_001165780.1:n.*81_*83del
NM_144573.4:c.*81_*83del MANE Select NP_653174.3:n.*81_*83del