Canonical Allele Identifier: CA523833243
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs1433426129

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77917540_77917543del , CM000663.2:g.77917540_77917543del GRCh38
NC_000001.10:g.78383225_78383228del , CM000663.1:g.78383225_78383228del GRCh37
NC_000001.9:g.78155813_78155816del NCBI36
NG_016625.1:g.34026_34029del , LRG_442:g.34026_34029del

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.28-26_28-23del MANE Select ENSP00000333938.7:n.28-26_28-23del
ENST00000330010.12:c.28-420_28-417del ENSP00000327363.8:n.28-420_28-417del
ENST00000334785.11:c.28-26_28-23del ENSP00000333938.7:n.28-26_28-23del
ENST00000401035.7:c.28-420_28-417del ENSP00000383814.3:n.28-420_28-417del
ENST00000440324.5:c.28-26_28-23del ENSP00000411902.1:n.28-26_28-23del
NM_001172309.1:c.28-420_28-417del NP_001165780.1:n.28-420_28-417del
NM_144573.3:c.28-26_28-23del , LRG_442t1:c.28-26_28-23del NP_653174.3:n.28-26_28-23del
XM_005271322.2:c.28-26_28-23del XP_005271379.1:n.28-26_28-23del
XM_005271323.2:c.28-26_28-23del XP_005271380.1:n.28-26_28-23del
XM_005271324.3:c.28-420_28-417del XP_005271381.1:n.28-420_28-417del
XM_005271325.2:c.28-26_28-23del XP_005271382.1:n.28-26_28-23del
XM_005271326.2:c.28-420_28-417del XP_005271383.1:n.28-420_28-417del
XM_005271327.2:c.28-26_28-23del XP_005271384.1:n.28-26_28-23del
XM_005271322.4:c.28-26_28-23del XP_005271379.1:n.28-26_28-23del
XM_005271323.4:c.28-26_28-23del XP_005271380.1:n.28-26_28-23del
XM_005271324.5:c.28-420_28-417del XP_005271381.1:n.28-420_28-417del
XM_005271325.4:c.28-26_28-23del XP_005271382.1:n.28-26_28-23del
XM_005271326.4:c.28-420_28-417del XP_005271383.1:n.28-420_28-417del
XM_005271327.4:c.28-26_28-23del XP_005271384.1:n.28-26_28-23del
NM_001172309.2:c.28-420_28-417del NP_001165780.1:n.28-420_28-417del
NM_144573.4:c.28-26_28-23del MANE Select NP_653174.3:n.28-26_28-23del