Canonical Allele Identifier: CA1801422840
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953391T= , CM000670.2:g.89953391T= GRCh38
NC_000008.10:g.90965619T= , CM000670.1:g.90965619T= GRCh37
NC_000008.9:g.91034795T= NCBI36
NG_008860.1:g.36281A= , LRG_158:g.36281A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3000A=
ENST00000517337.2:c.1452A= ENSP00000429971.2:p.Leu484=
ENST00000523444.2:c.1452A= ENSP00000428252.2:p.Leu484=
ENST00000697292.1:c.1698A= ENSP00000513229.1:p.Leu566=
ENST00000697293.1:c.1698A= ENSP00000513230.1:p.Leu566=
ENST00000697294.1:c.*1309A= ENSP00000513231.1:n.*1309A=
ENST00000697295.1:c.*1007A= ENSP00000513232.1:n.*1007A=
ENST00000697296.1:c.*1366A= ENSP00000513233.1:n.*1366A=
ENST00000697297.1:n.3483A=
ENST00000697298.1:c.1452A= ENSP00000513234.1:p.Leu484=
ENST00000697299.1:c.1452A= ENSP00000513235.1:p.Leu484=
ENST00000697300.1:c.*1302A= ENSP00000513236.1:n.*1302A=
ENST00000697301.1:c.*1219A= ENSP00000513237.1:n.*1219A=
ENST00000697302.1:c.*1219A= ENSP00000513238.1:n.*1219A=
ENST00000697303.1:c.*1302A= ENSP00000513239.1:n.*1302A=
ENST00000697304.1:c.1386A= ENSP00000513240.1:p.Leu462=
ENST00000697306.1:c.*698A= ENSP00000513241.1:n.*698A=
ENST00000697307.1:c.1698A= ENSP00000513242.1:p.Leu566=
ENST00000697308.1:c.1698A= ENSP00000513243.1:p.Leu566=
ENST00000697309.1:c.1698A= ENSP00000513244.1:p.Leu566=
ENST00000697310.1:c.1698A= ENSP00000513245.1:p.Leu566=
ENST00000697311.1:c.1698A= ENSP00000513246.1:p.Leu566=
ENST00000697312.1:c.*1096A= ENSP00000513247.1:n.*1096A=
ENST00000697313.1:n.2687+16973A=
ENST00000697314.1:n.3489A=
ENST00000697315.1:c.1698A= ENSP00000513248.1:p.Leu566=
ENST00000697316.1:n.1819A=
ENST00000697317.1:n.1808A=
ENST00000697318.1:n.1810A=
ENST00000265433.8:c.1698A= MANE Select ENSP00000265433.4:p.Leu566=
ENST00000265433.7:c.1698A= ENSP00000265433.3:p.Leu566=
ENST00000396252.6:c.*1571A= ENSP00000379551.2:n.*1571A=
ENST00000409330.5:c.1452A= ENSP00000386924.1:p.Leu484=
NM_001024688.2:c.1452A= NP_001019859.1:p.Leu484=
NM_002485.4:c.1698A= , LRG_158t1:c.1698A= NP_002476.2:p.Leu566=
XM_011517044.1:c.1674A= XP_011515346.1:p.Leu558=
XM_011517045.1:c.1452A= XP_011515347.1:p.Leu484=
XR_928335.1:n.1837A=
XM_017013460.1:c.819A= XP_016868949.1:p.Leu273=
XM_017013462.2:c.819A= XP_016868951.1:p.Leu273=
XM_024447163.1:c.1452A= XP_024302931.1:p.Leu484=
XM_024447164.1:c.1452A= XP_024302932.1:p.Leu484=
XM_024447165.1:c.819A= XP_024302933.1:p.Leu273=
NM_002485.5:c.1698A= MANE Select NP_002476.2:p.Leu566=
NM_001024688.3:c.1452A= NP_001019859.1:p.Leu484=