Canonical Allele Identifier: CA1801422566
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89952805_89952806delinsAT , CM000670.2:g.89952805_89952806delinsAT GRCh38
NC_000008.10:g.90965033_90965034delinsAT , CM000670.1:g.90965033_90965034delinsAT GRCh37
NC_000008.9:g.91034209_91034210delinsAT NCBI36
NG_008860.1:g.36866_36867delinsAT , LRG_158:g.36866_36867delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3147+438_3147+439delinsAT
ENST00000517337.2:c.1599+438_1599+439delinsAT ENSP00000429971.2:n.1599+438_1599+439delinsAT
ENST00000523444.2:c.1599+438_1599+439delinsAT ENSP00000428252.2:n.1599+438_1599+439delinsAT
ENST00000697292.1:c.1845+438_1845+439delinsAT ENSP00000513229.1:n.1845+438_1845+439delinsAT
ENST00000697293.1:c.1845+438_1845+439delinsAT ENSP00000513230.1:n.1845+438_1845+439delinsAT
ENST00000697294.1:c.*1456+438_*1456+439delinsAT ENSP00000513231.1:n.*1456+438_*1456+439delinsAT
ENST00000697295.1:c.*1154+438_*1154+439delinsAT ENSP00000513232.1:n.*1154+438_*1154+439delinsAT
ENST00000697296.1:c.*1513+438_*1513+439delinsAT ENSP00000513233.1:n.*1513+438_*1513+439delinsAT
ENST00000697297.1:n.3630+438_3630+439delinsAT
ENST00000697298.1:c.1599+438_1599+439delinsAT ENSP00000513234.1:n.1599+438_1599+439delinsAT
ENST00000697299.1:c.1599+438_1599+439delinsAT ENSP00000513235.1:n.1599+438_1599+439delinsAT
ENST00000697300.1:c.*1449+438_*1449+439delinsAT ENSP00000513236.1:n.*1449+438_*1449+439delinsAT
ENST00000697301.1:c.*1366+438_*1366+439delinsAT ENSP00000513237.1:n.*1366+438_*1366+439delinsAT
ENST00000697302.1:c.*1366+438_*1366+439delinsAT ENSP00000513238.1:n.*1366+438_*1366+439delinsAT
ENST00000697303.1:c.*1449+438_*1449+439delinsAT ENSP00000513239.1:n.*1449+438_*1449+439delinsAT
ENST00000697304.1:c.1533+438_1533+439delinsAT ENSP00000513240.1:n.1533+438_1533+439delinsAT
ENST00000697306.1:c.*845+438_*845+439delinsAT ENSP00000513241.1:n.*845+438_*845+439delinsAT
ENST00000697307.1:c.1845+438_1845+439delinsAT ENSP00000513242.1:n.1845+438_1845+439delinsAT
ENST00000697308.1:c.1845+438_1845+439delinsAT ENSP00000513243.1:n.1845+438_1845+439delinsAT
ENST00000697309.1:c.1845+438_1845+439delinsAT ENSP00000513244.1:n.1845+438_1845+439delinsAT
ENST00000697310.1:c.1845+438_1845+439delinsAT ENSP00000513245.1:n.1845+438_1845+439delinsAT
ENST00000697311.1:c.1845+438_1845+439delinsAT ENSP00000513246.1:n.1845+438_1845+439delinsAT
ENST00000697312.1:c.*1243+438_*1243+439delinsAT ENSP00000513247.1:n.*1243+438_*1243+439delinsAT
ENST00000697313.1:n.2688-17194_2688-17193delinsAT
ENST00000697314.1:n.3636+438_3636+439delinsAT
ENST00000697315.1:c.1845+438_1845+439delinsAT ENSP00000513248.1:n.1845+438_1845+439delinsAT
ENST00000697316.1:n.1966+438_1966+439delinsAT
ENST00000697317.1:n.1955+438_1955+439delinsAT
ENST00000265433.8:c.1845+438_1845+439delinsAT MANE Select ENSP00000265433.4:n.1845+438_1845+439delinsAT
ENST00000265433.7:c.1845+438_1845+439delinsAT ENSP00000265433.3:n.1845+438_1845+439delinsAT
ENST00000396252.6:c.*1718+438_*1718+439delinsAT ENSP00000379551.2:n.*1718+438_*1718+439delinsAT
ENST00000409330.5:c.1599+438_1599+439delinsAT ENSP00000386924.1:n.1599+438_1599+439delinsAT
ENST00000613033.1:c.111+438_111+439delinsAT ENSP00000484487.1:n.111+438_111+439delinsAT
NM_001024688.2:c.1599+438_1599+439delinsAT NP_001019859.1:n.1599+438_1599+439delinsAT
NM_002485.4:c.1845+438_1845+439delinsAT , LRG_158t1:c.1845+438_1845+439delinsAT NP_002476.2:n.1845+438_1845+439delinsAT
XM_011517044.1:c.1821+438_1821+439delinsAT XP_011515346.1:n.1821+438_1821+439delinsAT
XM_011517045.1:c.1599+438_1599+439delinsAT XP_011515347.1:n.1599+438_1599+439delinsAT
XR_928335.1:n.1984+438_1984+439delinsAT
XM_017013460.1:c.966+438_966+439delinsAT XP_016868949.1:n.966+438_966+439delinsAT
XM_017013462.2:c.966+438_966+439delinsAT XP_016868951.1:n.966+438_966+439delinsAT
XM_024447163.1:c.1599+438_1599+439delinsAT XP_024302931.1:n.1599+438_1599+439delinsAT
XM_024447164.1:c.1599+438_1599+439delinsAT XP_024302932.1:n.1599+438_1599+439delinsAT
XM_024447165.1:c.966+438_966+439delinsAT XP_024302933.1:n.966+438_966+439delinsAT
NM_002485.5:c.1845+438_1845+439delinsAT MANE Select NP_002476.2:n.1845+438_1845+439delinsAT
NM_001024688.3:c.1599+438_1599+439delinsAT NP_001019859.1:n.1599+438_1599+439delinsAT