Canonical Allele Identifier: CA1801422962
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953596G= , CM000670.2:g.89953596G= GRCh38
NC_000008.10:g.90965824G= , CM000670.1:g.90965824G= GRCh37
NC_000008.9:g.91035000G= NCBI36
NG_008860.1:g.36076C= , LRG_158:g.36076C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2795C=
ENST00000517337.2:c.1247C= ENSP00000429971.2:p.Pro416=
ENST00000523444.2:c.1247C= ENSP00000428252.2:p.Pro416=
ENST00000697292.1:c.1493C= ENSP00000513229.1:p.Pro498=
ENST00000697293.1:c.1493C= ENSP00000513230.1:p.Pro498=
ENST00000697294.1:c.*1104C= ENSP00000513231.1:n.*1104C=
ENST00000697295.1:c.*802C= ENSP00000513232.1:n.*802C=
ENST00000697296.1:c.*1161C= ENSP00000513233.1:n.*1161C=
ENST00000697297.1:n.3278C=
ENST00000697298.1:c.1247C= ENSP00000513234.1:p.Pro416=
ENST00000697299.1:c.1247C= ENSP00000513235.1:p.Pro416=
ENST00000697300.1:c.*1097C= ENSP00000513236.1:n.*1097C=
ENST00000697301.1:c.*1014C= ENSP00000513237.1:n.*1014C=
ENST00000697302.1:c.*1014C= ENSP00000513238.1:n.*1014C=
ENST00000697303.1:c.*1097C= ENSP00000513239.1:n.*1097C=
ENST00000697304.1:c.1181C= ENSP00000513240.1:p.Pro394=
ENST00000697306.1:c.*493C= ENSP00000513241.1:n.*493C=
ENST00000697307.1:c.1493C= ENSP00000513242.1:p.Pro498=
ENST00000697308.1:c.1493C= ENSP00000513243.1:p.Pro498=
ENST00000697309.1:c.1493C= ENSP00000513244.1:p.Pro498=
ENST00000697310.1:c.1493C= ENSP00000513245.1:p.Pro498=
ENST00000697311.1:c.1493C= ENSP00000513246.1:p.Pro498=
ENST00000697312.1:c.*891C= ENSP00000513247.1:n.*891C=
ENST00000697313.1:n.2687+16768C=
ENST00000697314.1:n.3284C=
ENST00000697315.1:c.1493C= ENSP00000513248.1:p.Pro498=
ENST00000697316.1:n.1614C=
ENST00000697317.1:n.1603C=
ENST00000697318.1:n.1605C=
ENST00000265433.8:c.1493C= MANE Select ENSP00000265433.4:p.Pro498=
ENST00000265433.7:c.1493C= ENSP00000265433.3:p.Pro498=
ENST00000396252.6:c.*1366C= ENSP00000379551.2:n.*1366C=
ENST00000409330.5:c.1247C= ENSP00000386924.1:p.Pro416=
NM_001024688.2:c.1247C= NP_001019859.1:p.Pro416=
NM_002485.4:c.1493C= , LRG_158t1:c.1493C= NP_002476.2:p.Pro498=
XM_011517044.1:c.1469C= XP_011515346.1:p.Pro490=
XM_011517045.1:c.1247C= XP_011515347.1:p.Pro416=
XR_928335.1:n.1632C=
XM_017013460.1:c.614C= XP_016868949.1:p.Pro205=
XM_017013462.2:c.614C= XP_016868951.1:p.Pro205=
XM_024447163.1:c.1247C= XP_024302931.1:p.Pro416=
XM_024447164.1:c.1247C= XP_024302932.1:p.Pro416=
XM_024447165.1:c.614C= XP_024302933.1:p.Pro205=
NM_002485.5:c.1493C= MANE Select NP_002476.2:p.Pro498=
NM_001024688.3:c.1247C= NP_001019859.1:p.Pro416=