Canonical Allele Identifier: CA1801420204
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89947700C= , CM000670.2:g.89947700C= GRCh38
NC_000008.10:g.90959928C= , CM000670.1:g.90959928C= GRCh37
NC_000008.9:g.91029104C= NCBI36
NG_008860.1:g.41972G= , LRG_158:g.41972G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3216+124G=
ENST00000517337.2:c.1668+124G= ENSP00000429971.2:n.1668+124G=
ENST00000523444.2:c.1668+124G= ENSP00000428252.2:n.1668+124G=
ENST00000697292.1:c.1914+124G= ENSP00000513229.1:n.1914+124G=
ENST00000697293.1:c.1914+124G= ENSP00000513230.1:n.1914+124G=
ENST00000697294.1:c.*1525+124G= ENSP00000513231.1:n.*1525+124G=
ENST00000697295.1:c.*1223+124G= ENSP00000513232.1:n.*1223+124G=
ENST00000697296.1:c.*1582+124G= ENSP00000513233.1:n.*1582+124G=
ENST00000697297.1:n.3699+124G=
ENST00000697298.1:c.1668+124G= ENSP00000513234.1:n.1668+124G=
ENST00000697299.1:c.1668+124G= ENSP00000513235.1:n.1668+124G=
ENST00000697300.1:c.*1518+124G= ENSP00000513236.1:n.*1518+124G=
ENST00000697301.1:c.*1435+124G= ENSP00000513237.1:n.*1435+124G=
ENST00000697302.1:c.*1435+124G= ENSP00000513238.1:n.*1435+124G=
ENST00000697303.1:c.*1518+124G= ENSP00000513239.1:n.*1518+124G=
ENST00000697304.1:c.1602+124G= ENSP00000513240.1:n.1602+124G=
ENST00000697306.1:c.*1061G= ENSP00000513241.1:n.*1061G=
ENST00000697307.1:c.1846-4334G= ENSP00000513242.1:n.1846-4334G=
ENST00000697308.1:c.1846-1405G= ENSP00000513243.1:n.1846-1405G=
ENST00000697309.1:c.1914+124G= ENSP00000513244.1:n.1914+124G=
ENST00000697310.1:c.1914+124G= ENSP00000513245.1:n.1914+124G=
ENST00000697311.1:c.1914+124G= ENSP00000513246.1:n.1914+124G=
ENST00000697312.1:c.*1312+124G= ENSP00000513247.1:n.*1312+124G=
ENST00000697313.1:n.2688-12088G=
ENST00000697314.1:n.3636+5544G=
ENST00000697315.1:c.1914+124G= ENSP00000513248.1:n.1914+124G=
ENST00000697316.1:n.2035+124G=
ENST00000697317.1:n.2005+143G=
ENST00000265433.8:c.1914+124G= MANE Select ENSP00000265433.4:n.1914+124G=
ENST00000265433.7:c.1914+124G= ENSP00000265433.3:n.1914+124G=
ENST00000396252.6:c.*1787+124G= ENSP00000379551.2:n.*1787+124G=
ENST00000409330.5:c.1668+124G= ENSP00000386924.1:n.1668+124G=
ENST00000613033.1:c.180+124G= ENSP00000484487.1:n.180+124G=
NM_001024688.2:c.1668+124G= NP_001019859.1:n.1668+124G=
NM_002485.4:c.1914+124G= , LRG_158t1:c.1914+124G= NP_002476.2:n.1914+124G=
XM_011517044.1:c.1890+124G= XP_011515346.1:n.1890+124G=
XM_011517045.1:c.1668+124G= XP_011515347.1:n.1668+124G=
XR_928335.1:n.2053+124G=
XM_017013460.1:c.1035+124G= XP_016868949.1:n.1035+124G=
XM_017013462.2:c.1035+124G= XP_016868951.1:n.1035+124G=
XM_024447163.1:c.1668+124G= XP_024302931.1:n.1668+124G=
XM_024447164.1:c.1668+124G= XP_024302932.1:n.1668+124G=
XM_024447165.1:c.1035+124G= XP_024302933.1:n.1035+124G=
NM_002485.5:c.1914+124G= MANE Select NP_002476.2:n.1914+124G=
NM_001024688.3:c.1668+124G= NP_001019859.1:n.1668+124G=