Canonical Allele Identifier: CA1801419514
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89946202T= , CM000670.2:g.89946202T= GRCh38
NC_000008.10:g.90958430T= , CM000670.1:g.90958430T= GRCh37
NC_000008.9:g.91027606T= NCBI36
NG_008860.1:g.43470A= , LRG_158:g.43470A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3310A=
ENST00000517337.2:c.1762A= ENSP00000429971.2:p.Arg588=
ENST00000523444.2:c.1762A= ENSP00000428252.2:p.Arg588=
ENST00000697292.1:c.2008A= ENSP00000513229.1:p.Arg670=
ENST00000697293.1:c.2008A= ENSP00000513230.1:p.Arg670=
ENST00000697294.1:c.*1619A= ENSP00000513231.1:n.*1619A=
ENST00000697295.1:c.*1317A= ENSP00000513232.1:n.*1317A=
ENST00000697296.1:c.*1676A= ENSP00000513233.1:n.*1676A=
ENST00000697297.1:n.3793A=
ENST00000697298.1:c.1762A= ENSP00000513234.1:p.Arg588=
ENST00000697299.1:c.1762A= ENSP00000513235.1:p.Arg588=
ENST00000697300.1:c.*1612A= ENSP00000513236.1:n.*1612A=
ENST00000697301.1:c.*1529A= ENSP00000513237.1:n.*1529A=
ENST00000697302.1:c.*1529A= ENSP00000513238.1:n.*1529A=
ENST00000697303.1:c.*1612A= ENSP00000513239.1:n.*1612A=
ENST00000697304.1:c.1696A= ENSP00000513240.1:p.Arg566=
ENST00000697306.1:c.*2559A= ENSP00000513241.1:n.*2559A=
ENST00000697307.1:c.1846-2836A= ENSP00000513242.1:n.1846-2836A=
ENST00000697308.1:c.1939A= ENSP00000513243.1:p.Arg647=
ENST00000697309.1:c.2008A= ENSP00000513244.1:p.Arg670=
ENST00000697310.1:c.2008A= ENSP00000513245.1:p.Arg670=
ENST00000697311.1:c.2008A= ENSP00000513246.1:p.Arg670=
ENST00000697312.1:c.*1406A= ENSP00000513247.1:n.*1406A=
ENST00000697313.1:n.2688-10590A=
ENST00000697314.1:n.3636+7042A=
ENST00000697315.1:c.2008A= ENSP00000513248.1:p.Arg670=
ENST00000697316.1:n.2129A=
ENST00000697317.1:n.2099A=
ENST00000265433.8:c.2008A= MANE Select ENSP00000265433.4:p.Arg670=
ENST00000265433.7:c.2008A= ENSP00000265433.3:p.Arg670=
ENST00000396252.6:c.*1881A= ENSP00000379551.2:n.*1881A=
ENST00000409330.5:c.1762A= ENSP00000386924.1:p.Arg588=
ENST00000520325.1:n.424A=
ENST00000613033.1:c.180+1622A= ENSP00000484487.1:n.180+1622A=
NM_001024688.2:c.1762A= NP_001019859.1:p.Arg588=
NM_002485.4:c.2008A= , LRG_158t1:c.2008A= NP_002476.2:p.Arg670=
XM_011517044.1:c.1984A= XP_011515346.1:p.Arg662=
XM_011517045.1:c.1762A= XP_011515347.1:p.Arg588=
XM_017013460.1:c.1129A= XP_016868949.1:p.Arg377=
XM_017013462.2:c.1129A= XP_016868951.1:p.Arg377=
XM_024447163.1:c.1762A= XP_024302931.1:p.Arg588=
XM_024447164.1:c.1762A= XP_024302932.1:p.Arg588=
XM_024447165.1:c.1129A= XP_024302933.1:p.Arg377=
NM_002485.5:c.2008A= MANE Select NP_002476.2:p.Arg670=
NM_001024688.3:c.1762A= NP_001019859.1:p.Arg588=