Canonical Allele Identifier: CA1801505575
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89970433G= , CM000670.2:g.89970433G= GRCh38
NC_000008.10:g.90982661G= , CM000670.1:g.90982661G= GRCh37
NC_000008.9:g.91051837G= NCBI36
NG_008860.1:g.19239C= , LRG_158:g.19239C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2129C=
ENST00000517337.2:c.581C= ENSP00000429971.2:p.Thr194=
ENST00000523444.2:c.581C= ENSP00000428252.2:p.Thr194=
ENST00000697292.1:c.827C= ENSP00000513229.1:p.Thr276=
ENST00000697293.1:c.827C= ENSP00000513230.1:p.Thr276=
ENST00000697294.1:c.*438C= ENSP00000513231.1:n.*438C=
ENST00000697295.1:c.*136C= ENSP00000513232.1:n.*136C=
ENST00000697296.1:c.*495C= ENSP00000513233.1:n.*495C=
ENST00000697297.1:n.2612C=
ENST00000697298.1:c.581C= ENSP00000513234.1:p.Thr194=
ENST00000697299.1:c.581C= ENSP00000513235.1:p.Thr194=
ENST00000697300.1:c.*431C= ENSP00000513236.1:n.*431C=
ENST00000697301.1:c.*348C= ENSP00000513237.1:n.*348C=
ENST00000697302.1:c.*348C= ENSP00000513238.1:n.*348C=
ENST00000697303.1:c.*431C= ENSP00000513239.1:n.*431C=
ENST00000697304.1:c.585-5926C= ENSP00000513240.1:n.585-5926C=
ENST00000697306.1:c.480+10301C= ENSP00000513241.1:n.480+10301C=
ENST00000697307.1:c.827C= ENSP00000513242.1:p.Thr276=
ENST00000697308.1:c.827C= ENSP00000513243.1:p.Thr276=
ENST00000697309.1:c.827C= ENSP00000513244.1:p.Thr276=
ENST00000697310.1:c.827C= ENSP00000513245.1:p.Thr276=
ENST00000697311.1:c.827C= ENSP00000513246.1:p.Thr276=
ENST00000697312.1:c.*225C= ENSP00000513247.1:n.*225C=
ENST00000697313.1:n.2618C=
ENST00000697314.1:n.2618C=
ENST00000697315.1:c.827C= ENSP00000513248.1:p.Thr276=
ENST00000697316.1:n.948C=
ENST00000697317.1:n.937C=
ENST00000697318.1:n.939C=
ENST00000265433.8:c.827C= MANE Select ENSP00000265433.4:p.Thr276=
ENST00000265433.7:c.827C= ENSP00000265433.3:p.Thr276=
ENST00000396252.6:c.*700C= ENSP00000379551.2:n.*700C=
ENST00000409330.5:c.581C= ENSP00000386924.1:p.Thr194=
NM_001024688.2:c.581C= NP_001019859.1:p.Thr194=
NM_002485.4:c.827C= , LRG_158t1:c.827C= NP_002476.2:p.Thr276=
XM_011517044.1:c.803C= XP_011515346.1:p.Thr268=
XM_011517045.1:c.581C= XP_011515347.1:p.Thr194=
XM_011517046.1:c.827C= XP_011515348.1:p.Thr276=
XR_928335.1:n.964C=
XM_017013460.1:c.-53C= XP_016868949.1:n.-53C=
XM_017013462.2:c.-53C= XP_016868951.1:n.-53C=
XM_024447163.1:c.581C= XP_024302931.1:p.Thr194=
XM_024447164.1:c.581C= XP_024302932.1:p.Thr194=
XM_024447165.1:c.-53C= XP_024302933.1:n.-53C=
NM_002485.5:c.827C= MANE Select NP_002476.2:p.Thr276=
NM_001024688.3:c.581C= NP_001019859.1:p.Thr194=