Canonical Allele Identifier: CA2717884363
Gene: NBN HGNC NCBI

Linked Data

dbSNP Id: rs2129936586

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89984398_89984399insATTCTGCGACCG , CM000670.2:g.89984398_89984399insATTCTGCGACCG GRCh38
NC_000008.10:g.90996626_90996627insATTCTGCGACCG , CM000670.1:g.90996626_90996627insATTCTGCGACCG GRCh37
NC_000008.9:g.91065802_91065803insATTCTGCGACCG NCBI36
NG_008860.1:g.5276_5277insTCGCAGAATCGG , LRG_158:g.5276_5277insTCGCAGAATCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.141+129_141+130insTCGCAGAATCGG
ENST00000523444.2:c.-260+129_-260+130insTCGCAGAATCGG ENSP00000428252.2:n.-260+129_-260+130insTCGCAGAATCGG
ENST00000697292.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513229.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697293.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513230.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697294.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513231.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697295.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513232.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697296.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513233.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697297.1:n.143+129_143+130insTCGCAGAATCGG
ENST00000697298.1:c.-443+129_-443+130insTCGCAGAATCGG ENSP00000513234.1:n.-443+129_-443+130insTCGCAGAATCGG
ENST00000697299.1:c.-76+129_-76+130insTCGCAGAATCGG ENSP00000513235.1:n.-76+129_-76+130insTCGCAGAATCGG
ENST00000697300.1:c.-260+129_-260+130insTCGCAGAATCGG ENSP00000513236.1:n.-260+129_-260+130insTCGCAGAATCGG
ENST00000697301.1:c.-260+129_-260+130insTCGCAGAATCGG ENSP00000513237.1:n.-260+129_-260+130insTCGCAGAATCGG
ENST00000697302.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513238.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697303.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513239.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697304.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513240.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697306.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513241.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697307.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513242.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697308.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513243.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697309.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513244.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697310.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513245.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697311.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513246.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697312.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513247.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697313.1:n.149+129_149+130insTCGCAGAATCGG
ENST00000697314.1:n.149+129_149+130insTCGCAGAATCGG
ENST00000697315.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000513248.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000697316.1:n.158+129_158+130insTCGCAGAATCGG
ENST00000697317.1:n.147+129_147+130insTCGCAGAATCGG
ENST00000697318.1:n.149+129_149+130insTCGCAGAATCGG
ENST00000265433.8:c.37+129_37+130insTCGCAGAATCGG MANE Select ENSP00000265433.4:n.37+129_37+130insTCGCAGAATCGG
ENST00000265433.7:c.37+129_37+130insTCGCAGAATCGG ENSP00000265433.3:n.37+129_37+130insTCGCAGAATCGG
ENST00000396252.6:c.37+129_37+130insTCGCAGAATCGG ENSP00000379551.2:n.37+129_37+130insTCGCAGAATCGG
ENST00000409330.5:c.-398_-397insTCGCAGAATCGG ENSP00000386924.1:n.-398_-397insTCGCAGAATCGG
ENST00000494804.1:n.141+129_141+130insTCGCAGAATCGG
ENST00000519426.5:c.37+129_37+130insTCGCAGAATCGG ENSP00000430983.1:n.37+129_37+130insTCGCAGAATCGG
ENST00000523444.1:c.37+129_37+130insTCGCAGAATCGG ENSP00000428252.1:n.37+129_37+130insTCGCAGAATCGG
NM_001024688.2:c.-260+129_-260+130insTCGCAGAATCGG NP_001019859.1:n.-260+129_-260+130insTCGCAGAATCGG
NM_002485.4:c.37+129_37+130insTCGCAGAATCGG , LRG_158t1:c.37+129_37+130insTCGCAGAATCGG NP_002476.2:n.37+129_37+130insTCGCAGAATCGG
XM_011517046.1:c.37+129_37+130insTCGCAGAATCGG XP_011515348.1:n.37+129_37+130insTCGCAGAATCGG
XR_928335.1:n.174+129_174+130insTCGCAGAATCGG
XM_017013460.1:c.-983+129_-983+130insTCGCAGAATCGG XP_016868949.1:n.-983+129_-983+130insTCGCAGAATCGG
XM_017013462.2:c.-789+129_-789+130insTCGCAGAATCGG XP_016868951.1:n.-789+129_-789+130insTCGCAGAATCGG
XM_024447165.1:c.-933+129_-933+130insTCGCAGAATCGG XP_024302933.1:n.-933+129_-933+130insTCGCAGAATCGG
NM_002485.5:c.37+129_37+130insTCGCAGAATCGG MANE Select NP_002476.2:n.37+129_37+130insTCGCAGAATCGG
NM_001024688.3:c.-260+129_-260+130insTCGCAGAATCGG NP_001019859.1:n.-260+129_-260+130insTCGCAGAATCGG