Canonical Allele Identifier: CA1801505244
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89970383T= , CM000670.2:g.89970383T= GRCh38
NC_000008.10:g.90982611T= , CM000670.1:g.90982611T= GRCh37
NC_000008.9:g.91051787T= NCBI36
NG_008860.1:g.19289A= , LRG_158:g.19289A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2179A=
ENST00000517337.2:c.631A= ENSP00000429971.2:p.Ile211=
ENST00000523444.2:c.631A= ENSP00000428252.2:p.Ile211=
ENST00000697292.1:c.877A= ENSP00000513229.1:p.Ile293=
ENST00000697293.1:c.877A= ENSP00000513230.1:p.Ile293=
ENST00000697294.1:c.*488A= ENSP00000513231.1:n.*488A=
ENST00000697295.1:c.*186A= ENSP00000513232.1:n.*186A=
ENST00000697296.1:c.*545A= ENSP00000513233.1:n.*545A=
ENST00000697297.1:n.2662A=
ENST00000697298.1:c.631A= ENSP00000513234.1:p.Ile211=
ENST00000697299.1:c.631A= ENSP00000513235.1:p.Ile211=
ENST00000697300.1:c.*481A= ENSP00000513236.1:n.*481A=
ENST00000697301.1:c.*398A= ENSP00000513237.1:n.*398A=
ENST00000697302.1:c.*398A= ENSP00000513238.1:n.*398A=
ENST00000697303.1:c.*481A= ENSP00000513239.1:n.*481A=
ENST00000697304.1:c.585-5876A= ENSP00000513240.1:n.585-5876A=
ENST00000697306.1:c.480+10351A= ENSP00000513241.1:n.480+10351A=
ENST00000697307.1:c.877A= ENSP00000513242.1:p.Ile293=
ENST00000697308.1:c.877A= ENSP00000513243.1:p.Ile293=
ENST00000697309.1:c.877A= ENSP00000513244.1:p.Ile293=
ENST00000697310.1:c.877A= ENSP00000513245.1:p.Ile293=
ENST00000697311.1:c.877A= ENSP00000513246.1:p.Ile293=
ENST00000697312.1:c.*275A= ENSP00000513247.1:n.*275A=
ENST00000697313.1:n.2668A=
ENST00000697314.1:n.2668A=
ENST00000697315.1:c.877A= ENSP00000513248.1:p.Ile293=
ENST00000697316.1:n.998A=
ENST00000697317.1:n.987A=
ENST00000697318.1:n.989A=
ENST00000265433.8:c.877A= MANE Select ENSP00000265433.4:p.Ile293=
ENST00000265433.7:c.877A= ENSP00000265433.3:p.Ile293=
ENST00000396252.6:c.*750A= ENSP00000379551.2:n.*750A=
ENST00000409330.5:c.631A= ENSP00000386924.1:p.Ile211=
NM_001024688.2:c.631A= NP_001019859.1:p.Ile211=
NM_002485.4:c.877A= , LRG_158t1:c.877A= NP_002476.2:p.Ile293=
XM_011517044.1:c.853A= XP_011515346.1:p.Ile285=
XM_011517045.1:c.631A= XP_011515347.1:p.Ile211=
XM_011517046.1:c.877A= XP_011515348.1:p.Ile293=
XR_928335.1:n.1014A=
XM_017013460.1:c.-3A= XP_016868949.1:n.-3A=
XM_017013462.2:c.-3A= XP_016868951.1:n.-3A=
XM_024447163.1:c.631A= XP_024302931.1:p.Ile211=
XM_024447164.1:c.631A= XP_024302932.1:p.Ile211=
XM_024447165.1:c.-3A= XP_024302933.1:n.-3A=
NM_002485.5:c.877A= MANE Select NP_002476.2:p.Ile293=
NM_001024688.3:c.631A= NP_001019859.1:p.Ile211=