Canonical Allele Identifier: CA1801415395
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89937030A= , CM000670.2:g.89937030A= GRCh38
NC_000008.10:g.90949258A= , CM000670.1:g.90949258A= GRCh37
NC_000008.9:g.91018434A= NCBI36
NG_008860.1:g.52642T= , LRG_158:g.52642T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474821.2:n.3650T=
ENST00000494804.2:n.3532T=
ENST00000517337.2:c.1984T= ENSP00000429971.2:p.Phe662=
ENST00000523444.2:c.1984T= ENSP00000428252.2:p.Phe662=
ENST00000697292.1:c.2230T= ENSP00000513229.1:p.Phe744=
ENST00000697293.1:c.2281T= ENSP00000513230.1:p.Phe761=
ENST00000697294.1:c.*1841T= ENSP00000513231.1:n.*1841T=
ENST00000697295.1:c.*1539T= ENSP00000513232.1:n.*1539T=
ENST00000697296.1:c.*1898T= ENSP00000513233.1:n.*1898T=
ENST00000697297.1:n.4015T=
ENST00000697298.1:c.1984T= ENSP00000513234.1:p.Phe662=
ENST00000697299.1:c.1984T= ENSP00000513235.1:p.Phe662=
ENST00000697300.1:c.*1834T= ENSP00000513236.1:n.*1834T=
ENST00000697301.1:c.*1751T= ENSP00000513237.1:n.*1751T=
ENST00000697302.1:c.*1751T= ENSP00000513238.1:n.*1751T=
ENST00000697303.1:c.*1834T= ENSP00000513239.1:n.*1834T=
ENST00000697304.1:c.1918T= ENSP00000513240.1:p.Phe640=
ENST00000697305.1:n.2497T=
ENST00000697306.1:c.*2781T= ENSP00000513241.1:n.*2781T=
ENST00000697307.1:c.2005T= ENSP00000513242.1:p.Phe669=
ENST00000697308.1:c.2161T= ENSP00000513243.1:p.Phe721=
ENST00000697309.1:c.2185-1418T= ENSP00000513244.1:n.2185-1418T=
ENST00000697310.1:c.2230T= ENSP00000513245.1:p.Phe744=
ENST00000697311.1:c.*495T= ENSP00000513246.1:n.*495T=
ENST00000697312.1:c.*1683T= ENSP00000513247.1:n.*1683T=
ENST00000697313.1:n.2688-1418T=
ENST00000697314.1:n.3637-1418T=
ENST00000697315.1:c.*134T= ENSP00000513248.1:n.*134T=
ENST00000697316.1:n.2351T=
ENST00000265433.8:c.2230T= MANE Select ENSP00000265433.4:p.Phe744=
ENST00000265433.7:c.2230T= ENSP00000265433.3:p.Phe744=
ENST00000396252.6:c.*2103T= ENSP00000379551.2:n.*2103T=
ENST00000409330.5:c.1984T= ENSP00000386924.1:p.Phe662=
ENST00000474821.1:n.318T=
ENST00000613033.1:c.340T= ENSP00000484487.1:p.Phe114=
NM_001024688.2:c.1984T= NP_001019859.1:p.Phe662=
NM_002485.4:c.2230T= , LRG_158t1:c.2230T= NP_002476.2:p.Phe744=
XM_011517044.1:c.2206T= XP_011515346.1:p.Phe736=
XM_011517045.1:c.1984T= XP_011515347.1:p.Phe662=
XM_017013460.1:c.1351T= XP_016868949.1:p.Phe451=
XM_017013462.2:c.1351T= XP_016868951.1:p.Phe451=
XM_024447163.1:c.1984T= XP_024302931.1:p.Phe662=
XM_024447164.1:c.1984T= XP_024302932.1:p.Phe662=
XM_024447165.1:c.1351T= XP_024302933.1:p.Phe451=
NM_002485.5:c.2230T= MANE Select NP_002476.2:p.Phe744=
NM_001024688.3:c.1984T= NP_001019859.1:p.Phe662=