Canonical Allele Identifier: CA1801505778
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89970466G= , CM000670.2:g.89970466G= GRCh38
NC_000008.10:g.90982694G= , CM000670.1:g.90982694G= GRCh37
NC_000008.9:g.91051870G= NCBI36
NG_008860.1:g.19206C= , LRG_158:g.19206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2096C=
ENST00000517337.2:c.548C= ENSP00000429971.2:p.Ala183=
ENST00000523444.2:c.548C= ENSP00000428252.2:p.Ala183=
ENST00000697292.1:c.794C= ENSP00000513229.1:p.Ala265=
ENST00000697293.1:c.794C= ENSP00000513230.1:p.Ala265=
ENST00000697294.1:c.*405C= ENSP00000513231.1:n.*405C=
ENST00000697295.1:c.*103C= ENSP00000513232.1:n.*103C=
ENST00000697296.1:c.*462C= ENSP00000513233.1:n.*462C=
ENST00000697297.1:n.2579C=
ENST00000697298.1:c.548C= ENSP00000513234.1:p.Ala183=
ENST00000697299.1:c.548C= ENSP00000513235.1:p.Ala183=
ENST00000697300.1:c.*398C= ENSP00000513236.1:n.*398C=
ENST00000697301.1:c.*315C= ENSP00000513237.1:n.*315C=
ENST00000697302.1:c.*315C= ENSP00000513238.1:n.*315C=
ENST00000697303.1:c.*398C= ENSP00000513239.1:n.*398C=
ENST00000697304.1:c.585-5959C= ENSP00000513240.1:n.585-5959C=
ENST00000697306.1:c.480+10268C= ENSP00000513241.1:n.480+10268C=
ENST00000697307.1:c.794C= ENSP00000513242.1:p.Ala265=
ENST00000697308.1:c.794C= ENSP00000513243.1:p.Ala265=
ENST00000697309.1:c.794C= ENSP00000513244.1:p.Ala265=
ENST00000697310.1:c.794C= ENSP00000513245.1:p.Ala265=
ENST00000697311.1:c.794C= ENSP00000513246.1:p.Ala265=
ENST00000697312.1:c.*192C= ENSP00000513247.1:n.*192C=
ENST00000697313.1:n.2585C=
ENST00000697314.1:n.2585C=
ENST00000697315.1:c.794C= ENSP00000513248.1:p.Ala265=
ENST00000697316.1:n.915C=
ENST00000697317.1:n.904C=
ENST00000697318.1:n.906C=
ENST00000265433.8:c.794C= MANE Select ENSP00000265433.4:p.Ala265=
ENST00000265433.7:c.794C= ENSP00000265433.3:p.Ala265=
ENST00000396252.6:c.*667C= ENSP00000379551.2:n.*667C=
ENST00000409330.5:c.548C= ENSP00000386924.1:p.Ala183=
NM_001024688.2:c.548C= NP_001019859.1:p.Ala183=
NM_002485.4:c.794C= , LRG_158t1:c.794C= NP_002476.2:p.Ala265=
XM_011517044.1:c.770C= XP_011515346.1:p.Ala257=
XM_011517045.1:c.548C= XP_011515347.1:p.Ala183=
XM_011517046.1:c.794C= XP_011515348.1:p.Ala265=
XR_928335.1:n.931C=
XM_017013460.1:c.-86C= XP_016868949.1:n.-86C=
XM_017013462.2:c.-86C= XP_016868951.1:n.-86C=
XM_024447163.1:c.548C= XP_024302931.1:p.Ala183=
XM_024447164.1:c.548C= XP_024302932.1:p.Ala183=
XM_024447165.1:c.-86C= XP_024302933.1:n.-86C=
NM_002485.5:c.794C= MANE Select NP_002476.2:p.Ala265=
NM_001024688.3:c.548C= NP_001019859.1:p.Ala183=