Canonical Allele Identifier: CA583376805
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89982808del , CM000670.2:g.89982808del GRCh38
NC_000008.10:g.90995036del , CM000670.1:g.90995036del GRCh37
NC_000008.9:g.91064212del NCBI36
NG_008860.1:g.6868del , LRG_158:g.6868del

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.193del
ENST00000517337.2:c.-208del ENSP00000429971.2:n.-208del
ENST00000523444.2:c.-208del ENSP00000428252.2:n.-208del
ENST00000697292.1:c.89del ENSP00000513229.1:p.Asn30ThrfsTer5
ENST00000697293.1:c.89del ENSP00000513230.1:p.Asn30ThrfsTer5
ENST00000697294.1:c.89del ENSP00000513231.1:p.Asn30ThrfsTer5
ENST00000697295.1:c.37+1721del ENSP00000513232.1:n.37+1721del
ENST00000697296.1:c.89del ENSP00000513233.1:p.Asn30ThrfsTer5
ENST00000697297.1:n.195del
ENST00000697298.1:c.-208del ENSP00000513234.1:n.-208del
ENST00000697299.1:c.-75-1281del ENSP00000513235.1:n.-75-1281del
ENST00000697300.1:c.-208del ENSP00000513236.1:n.-208del
ENST00000697301.1:c.-208del ENSP00000513237.1:n.-208del
ENST00000697302.1:c.89del ENSP00000513238.1:p.Asn30ThrfsTer5
ENST00000697303.1:c.89del ENSP00000513239.1:p.Asn30ThrfsTer5
ENST00000697304.1:c.89del ENSP00000513240.1:p.Asn30ThrfsTer5
ENST00000697306.1:c.89del ENSP00000513241.1:p.Asn30ThrfsTer5
ENST00000697307.1:c.89del ENSP00000513242.1:p.Asn30ThrfsTer5
ENST00000697308.1:c.89del ENSP00000513243.1:p.Asn30ThrfsTer5
ENST00000697309.1:c.89del ENSP00000513244.1:p.Asn30ThrfsTer5
ENST00000697310.1:c.89del ENSP00000513245.1:p.Asn30ThrfsTer5
ENST00000697311.1:c.89del ENSP00000513246.1:p.Asn30ThrfsTer5
ENST00000697312.1:c.89del ENSP00000513247.1:p.Asn30ThrfsTer5
ENST00000697313.1:n.201del
ENST00000697314.1:n.201del
ENST00000697315.1:c.89del ENSP00000513248.1:p.Asn30ThrfsTer5
ENST00000697316.1:n.210del
ENST00000697317.1:n.199del
ENST00000697318.1:n.201del
ENST00000265433.8:c.89del MANE Select ENSP00000265433.4:p.Asn30ThrfsTer5
ENST00000265433.7:c.89del ENSP00000265433.3:p.Asn30ThrfsTer5
ENST00000396252.6:c.89del ENSP00000379551.2:p.Asn30ThrfsTer5
ENST00000409330.5:c.-158del ENSP00000386924.1:n.-158del
ENST00000494804.1:n.193del
ENST00000517337.1:c.-208del ENSP00000429971.1:n.-208del
ENST00000519426.5:c.89del ENSP00000430983.1:p.Asn30ThrfsTer5
ENST00000523444.1:c.89del ENSP00000428252.1:p.Asn30ThrfsTer5
NM_001024688.2:c.-208del NP_001019859.1:n.-208del
NM_002485.4:c.89del , LRG_158t1:c.89del NP_002476.2:p.Asn30ThrfsTer5
XM_011517044.1:c.65del XP_011515346.1:p.Asn22ThrfsTer5
XM_011517045.1:c.-208del XP_011515347.1:n.-208del
XM_011517046.1:c.89del XP_011515348.1:p.Asn30ThrfsTer5
XR_928335.1:n.226del
XM_017013460.1:c.-931del XP_016868949.1:n.-931del
XM_017013462.2:c.-737del XP_016868951.1:n.-737del
XM_024447163.1:c.-158del XP_024302931.1:n.-158del
XM_024447165.1:c.-881del XP_024302933.1:n.-881del
NM_002485.5:c.89del MANE Select NP_002476.2:p.Asn30ThrfsTer5
NM_001024688.3:c.-208del NP_001019859.1:n.-208del