Canonical Allele Identifier: CA1801422897
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953481G= , CM000670.2:g.89953481G= GRCh38
NC_000008.10:g.90965709G= , CM000670.1:g.90965709G= GRCh37
NC_000008.9:g.91034885G= NCBI36
NG_008860.1:g.36191C= , LRG_158:g.36191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2910C=
ENST00000517337.2:c.1362C= ENSP00000429971.2:p.Ala454=
ENST00000523444.2:c.1362C= ENSP00000428252.2:p.Ala454=
ENST00000697292.1:c.1608C= ENSP00000513229.1:p.Ala536=
ENST00000697293.1:c.1608C= ENSP00000513230.1:p.Ala536=
ENST00000697294.1:c.*1219C= ENSP00000513231.1:n.*1219C=
ENST00000697295.1:c.*917C= ENSP00000513232.1:n.*917C=
ENST00000697296.1:c.*1276C= ENSP00000513233.1:n.*1276C=
ENST00000697297.1:n.3393C=
ENST00000697298.1:c.1362C= ENSP00000513234.1:p.Ala454=
ENST00000697299.1:c.1362C= ENSP00000513235.1:p.Ala454=
ENST00000697300.1:c.*1212C= ENSP00000513236.1:n.*1212C=
ENST00000697301.1:c.*1129C= ENSP00000513237.1:n.*1129C=
ENST00000697302.1:c.*1129C= ENSP00000513238.1:n.*1129C=
ENST00000697303.1:c.*1212C= ENSP00000513239.1:n.*1212C=
ENST00000697304.1:c.1296C= ENSP00000513240.1:p.Ala432=
ENST00000697306.1:c.*608C= ENSP00000513241.1:n.*608C=
ENST00000697307.1:c.1608C= ENSP00000513242.1:p.Ala536=
ENST00000697308.1:c.1608C= ENSP00000513243.1:p.Ala536=
ENST00000697309.1:c.1608C= ENSP00000513244.1:p.Ala536=
ENST00000697310.1:c.1608C= ENSP00000513245.1:p.Ala536=
ENST00000697311.1:c.1608C= ENSP00000513246.1:p.Ala536=
ENST00000697312.1:c.*1006C= ENSP00000513247.1:n.*1006C=
ENST00000697313.1:n.2687+16883C=
ENST00000697314.1:n.3399C=
ENST00000697315.1:c.1608C= ENSP00000513248.1:p.Ala536=
ENST00000697316.1:n.1729C=
ENST00000697317.1:n.1718C=
ENST00000697318.1:n.1720C=
ENST00000265433.8:c.1608C= MANE Select ENSP00000265433.4:p.Ala536=
ENST00000265433.7:c.1608C= ENSP00000265433.3:p.Ala536=
ENST00000396252.6:c.*1481C= ENSP00000379551.2:n.*1481C=
ENST00000409330.5:c.1362C= ENSP00000386924.1:p.Ala454=
NM_001024688.2:c.1362C= NP_001019859.1:p.Ala454=
NM_002485.4:c.1608C= , LRG_158t1:c.1608C= NP_002476.2:p.Ala536=
XM_011517044.1:c.1584C= XP_011515346.1:p.Ala528=
XM_011517045.1:c.1362C= XP_011515347.1:p.Ala454=
XR_928335.1:n.1747C=
XM_017013460.1:c.729C= XP_016868949.1:p.Ala243=
XM_017013462.2:c.729C= XP_016868951.1:p.Ala243=
XM_024447163.1:c.1362C= XP_024302931.1:p.Ala454=
XM_024447164.1:c.1362C= XP_024302932.1:p.Ala454=
XM_024447165.1:c.729C= XP_024302933.1:p.Ala243=
NM_002485.5:c.1608C= MANE Select NP_002476.2:p.Ala536=
NM_001024688.3:c.1362C= NP_001019859.1:p.Ala454=