Canonical Allele Identifier: CA335472
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 201946
dbSNP Id: rs794729094

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77942827_77942830del , CM000663.2:g.77942827_77942830del GRCh38
NC_000001.10:g.78408512_78408515del , CM000663.1:g.78408512_78408515del GRCh37
NC_000001.9:g.78181100_78181103del NCBI36
NG_016625.1:g.59313_59316del , LRG_442:g.59313_59316del
NG_033243.2:g.41267_41270del

Transcript Alleles

HGVS Amino-acid change
ENST00000334785.12:c.2026_*1del MANE Select ENSP00000333938.7:n.[c.2026_*1del;Ter676H...
ENST00000330010.12:c.1834_*1del ENSP00000327363.8:n.[c.1834_*1del;Ter612H...
ENST00000334785.11:c.2026_*1del ENSP00000333938.7:n.[c.2026_*1del;Ter676H...
ENST00000342754.5:c.1716+9_1716+12del
ENST00000480732.2:n.1600_1603del
NM_001172309.1:c.1834_*1del NP_001165780.1:n.[c.1834_*1del;Ter612Hise...
NM_144573.3:c.2026_*1del , LRG_442t1:c.2026_*1del NP_653174.3:n.[c.2026_*1del;Ter676HisextT...
XM_005271322.2:c.2017+9_2017+12del XP_005271379.1:n.2017+9_2017+12del
XM_005271323.2:c.1975+9_1975+12del XP_005271380.1:n.1975+9_1975+12del
XM_005271324.3:c.1825+9_1825+12del XP_005271381.1:n.1825+9_1825+12del
XM_005271325.2:c.1795+9_1795+12del XP_005271382.1:n.1795+9_1795+12del
XM_005271326.2:c.1783+9_1783+12del XP_005271383.1:n.1783+9_1783+12del
XM_005271327.2:c.1600+9_1600+12del XP_005271384.1:n.1600+9_1600+12del
XM_005271322.4:c.2017+9_2017+12del XP_005271379.1:n.2017+9_2017+12del
XM_005271323.4:c.1975+9_1975+12del XP_005271380.1:n.1975+9_1975+12del
XM_005271324.5:c.1825+9_1825+12del XP_005271381.1:n.1825+9_1825+12del
XM_005271325.4:c.1795+9_1795+12del XP_005271382.1:n.1795+9_1795+12del
XM_005271326.4:c.1783+9_1783+12del XP_005271383.1:n.1783+9_1783+12del
XM_005271327.4:c.1600+9_1600+12del XP_005271384.1:n.1600+9_1600+12del
NM_001172309.2:c.1834_*1del NP_001165780.1:n.[c.1834_*1del;Ter612Hise...
NM_144573.4:c.2026_*1del MANE Select NP_653174.3:n.[c.2026_*1del;Ter676HisextT...