Canonical Allele Identifier: CA1003480884
Gene: NEXN HGNC NCBI

Linked Data

dbSNP Id: rs1649050300

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77917245_77917246del , CM000663.2:g.77917245_77917246del GRCh38
NC_000001.10:g.78382930_78382931del , CM000663.1:g.78382930_78382931del GRCh37
NC_000001.9:g.78155518_78155519del NCBI36
NG_016625.1:g.33731_33732del , LRG_442:g.33731_33732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334785.12:c.28-321_28-320del MANE Select ENSP00000333938.7:n.28-321_28-320del
ENST00000330010.12:c.28-715_28-714del ENSP00000327363.8:n.28-715_28-714del
ENST00000334785.11:c.28-321_28-320del ENSP00000333938.7:n.28-321_28-320del
ENST00000401035.7:c.28-715_28-714del ENSP00000383814.3:n.28-715_28-714del
ENST00000440324.5:c.28-321_28-320del ENSP00000411902.1:n.28-321_28-320del
NM_001172309.1:c.28-715_28-714del NP_001165780.1:n.28-715_28-714del
NM_144573.3:c.28-321_28-320del , LRG_442t1:c.28-321_28-320del NP_653174.3:n.28-321_28-320del
XM_005271322.2:c.28-321_28-320del XP_005271379.1:n.28-321_28-320del
XM_005271323.2:c.28-321_28-320del XP_005271380.1:n.28-321_28-320del
XM_005271324.3:c.28-715_28-714del XP_005271381.1:n.28-715_28-714del
XM_005271325.2:c.28-321_28-320del XP_005271382.1:n.28-321_28-320del
XM_005271326.2:c.28-715_28-714del XP_005271383.1:n.28-715_28-714del
XM_005271327.2:c.28-321_28-320del XP_005271384.1:n.28-321_28-320del
XM_005271322.4:c.28-321_28-320del XP_005271379.1:n.28-321_28-320del
XM_005271323.4:c.28-321_28-320del XP_005271380.1:n.28-321_28-320del
XM_005271324.5:c.28-715_28-714del XP_005271381.1:n.28-715_28-714del
XM_005271325.4:c.28-321_28-320del XP_005271382.1:n.28-321_28-320del
XM_005271326.4:c.28-715_28-714del XP_005271383.1:n.28-715_28-714del
XM_005271327.4:c.28-321_28-320del XP_005271384.1:n.28-321_28-320del
NM_001172309.2:c.28-715_28-714del NP_001165780.1:n.28-715_28-714del
NM_144573.4:c.28-321_28-320del MANE Select NP_653174.3:n.28-321_28-320del