Canonical Allele Identifier: CA16618715
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 422213
dbSNP Id: rs1064795634

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89981480_89981483del , CM000670.2:g.89981480_89981483del GRCh38
NC_000008.10:g.90993708_90993711del , CM000670.1:g.90993708_90993711del GRCh37
NC_000008.9:g.91062884_91062887del NCBI36
NG_008860.1:g.8189_8192del , LRG_158:g.8189_8192del

Transcript Alleles

HGVS Amino-acid change
ENST00000494804.2:n.1514_1517del
ENST00000517337.2:c.-35_-32del ENSP00000429971.2:n.-35_-32del
ENST00000523444.2:c.-35_-32del ENSP00000428252.2:n.-35_-32del
ENST00000697292.1:c.212_215del ENSP00000513229.1:p.Asn71IlefsTer20
ENST00000697293.1:c.212_215del ENSP00000513230.1:p.Asn71IlefsTer20
ENST00000697294.1:c.212_215del ENSP00000513231.1:p.Asn71IlefsTer20
ENST00000697295.1:c.37+3042_37+3045del ENSP00000513232.1:n.37+3042_37+3045del
ENST00000697296.1:c.172-590_172-587del ENSP00000513233.1:n.172-590_172-587del
ENST00000697297.1:n.1516_1519del
ENST00000697298.1:c.-35_-32del ENSP00000513234.1:n.-35_-32del
ENST00000697299.1:c.-35_-32del ENSP00000513235.1:n.-35_-32del
ENST00000697300.1:c.-35_-32del ENSP00000513236.1:n.-35_-32del
ENST00000697301.1:c.-35_-32del ENSP00000513237.1:n.-35_-32del
ENST00000697302.1:c.212_215del ENSP00000513238.1:p.Asn71IlefsTer20
ENST00000697303.1:c.212_215del ENSP00000513239.1:p.Asn71IlefsTer20
ENST00000697304.1:c.212_215del ENSP00000513240.1:p.Asn71IlefsTer20
ENST00000697306.1:c.212_215del ENSP00000513241.1:p.Asn71IlefsTer20
ENST00000697307.1:c.212_215del ENSP00000513242.1:p.Asn71IlefsTer20
ENST00000697308.1:c.212_215del ENSP00000513243.1:p.Asn71IlefsTer20
ENST00000697309.1:c.212_215del ENSP00000513244.1:p.Asn71IlefsTer20
ENST00000697310.1:c.212_215del ENSP00000513245.1:p.Asn71IlefsTer20
ENST00000697311.1:c.212_215del ENSP00000513246.1:p.Asn71IlefsTer20
ENST00000697312.1:c.212_215del ENSP00000513247.1:p.Asn71IlefsTer20
ENST00000697313.1:n.1522_1525del
ENST00000697314.1:n.1522_1525del
ENST00000697315.1:c.212_215del ENSP00000513248.1:p.Asn71IlefsTer20
ENST00000697316.1:n.333_336del
ENST00000697317.1:n.322_325del
ENST00000697318.1:n.324_327del
ENST00000265433.8:c.212_215del MANE Select ENSP00000265433.4:p.Asn71IlefsTer20
ENST00000265433.7:c.212_215del ENSP00000265433.3:p.Asn71IlefsTer20
ENST00000396252.6:c.*85_*88del ENSP00000379551.2:n.*85_*88del
ENST00000409330.5:c.-35_-32del ENSP00000386924.1:n.-35_-32del
ENST00000517337.1:c.-35_-32del ENSP00000429971.1:n.-35_-32del
ENST00000517772.5:c.-35_-32del ENSP00000428717.1:n.-35_-32del
ENST00000519426.5:c.212_215del ENSP00000430983.1:p.Asn71IlefsTer20
ENST00000523444.1:c.*85_*88del ENSP00000428252.1:n.*85_*88del
NM_001024688.2:c.-35_-32del NP_001019859.1:n.-35_-32del
NM_002485.4:c.212_215del , LRG_158t1:c.212_215del NP_002476.2:p.Asn71IlefsTer20
XM_011517044.1:c.188_191del XP_011515346.1:p.Asn63IlefsTer20
XM_011517045.1:c.-35_-32del XP_011515347.1:n.-35_-32del
XM_011517046.1:c.212_215del XP_011515348.1:p.Asn71IlefsTer20
XR_928335.1:n.349_352del
XM_017013460.1:c.-758_-755del XP_016868949.1:n.-758_-755del
XM_017013462.2:c.-564_-561del XP_016868951.1:n.-564_-561del
XM_024447163.1:c.-35_-32del XP_024302931.1:n.-35_-32del
XM_024447164.1:c.-35_-32del XP_024302932.1:n.-35_-32del
XM_024447165.1:c.-758_-755del XP_024302933.1:n.-758_-755del
NM_002485.5:c.212_215del MANE Select NP_002476.2:p.Asn71IlefsTer20
NM_001024688.3:c.-35_-32del NP_001019859.1:n.-35_-32del