Canonical Allele Identifier: CA1801424824
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89955466T= , CM000670.2:g.89955466T= GRCh38
NC_000008.10:g.90967694T= , CM000670.1:g.90967694T= GRCh37
NC_000008.9:g.91036870T= NCBI36
NG_008860.1:g.34206A= , LRG_158:g.34206A=

Transcript Alleles

HGVS Amino-acid change
ENST00000494804.2:n.2516A=
ENST00000517337.2:c.968A= ENSP00000429971.2:p.Glu323=
ENST00000523444.2:c.968A= ENSP00000428252.2:p.Glu323=
ENST00000697292.1:c.1214A= ENSP00000513229.1:p.Glu405=
ENST00000697293.1:c.1214A= ENSP00000513230.1:p.Glu405=
ENST00000697294.1:c.*825A= ENSP00000513231.1:n.*825A=
ENST00000697295.1:c.*523A= ENSP00000513232.1:n.*523A=
ENST00000697296.1:c.*882A= ENSP00000513233.1:n.*882A=
ENST00000697297.1:n.2999A=
ENST00000697298.1:c.968A= ENSP00000513234.1:p.Glu323=
ENST00000697299.1:c.968A= ENSP00000513235.1:p.Glu323=
ENST00000697300.1:c.*818A= ENSP00000513236.1:n.*818A=
ENST00000697301.1:c.*735A= ENSP00000513237.1:n.*735A=
ENST00000697302.1:c.*735A= ENSP00000513238.1:n.*735A=
ENST00000697303.1:c.*818A= ENSP00000513239.1:n.*818A=
ENST00000697304.1:c.902A= ENSP00000513240.1:p.Glu301=
ENST00000697306.1:c.*214A= ENSP00000513241.1:n.*214A=
ENST00000697307.1:c.1214A= ENSP00000513242.1:p.Glu405=
ENST00000697308.1:c.1214A= ENSP00000513243.1:p.Glu405=
ENST00000697309.1:c.1214A= ENSP00000513244.1:p.Glu405=
ENST00000697310.1:c.1214A= ENSP00000513245.1:p.Glu405=
ENST00000697311.1:c.1214A= ENSP00000513246.1:p.Glu405=
ENST00000697312.1:c.*612A= ENSP00000513247.1:n.*612A=
ENST00000697313.1:n.2687+14898A=
ENST00000697314.1:n.3005A=
ENST00000697315.1:c.1214A= ENSP00000513248.1:p.Glu405=
ENST00000697316.1:n.1335A=
ENST00000697317.1:n.1324A=
ENST00000697318.1:n.1326A=
ENST00000265433.8:c.1214A= MANE Select ENSP00000265433.4:p.Glu405=
ENST00000265433.7:c.1214A= ENSP00000265433.3:p.Glu405=
ENST00000396252.6:c.*1087A= ENSP00000379551.2:n.*1087A=
ENST00000409330.5:c.968A= ENSP00000386924.1:p.Glu323=
NM_001024688.2:c.968A= NP_001019859.1:p.Glu323=
NM_002485.4:c.1214A= , LRG_158t1:c.1214A= NP_002476.2:p.Glu405=
XM_011517044.1:c.1190A= XP_011515346.1:p.Glu397=
XM_011517045.1:c.968A= XP_011515347.1:p.Glu323=
XM_011517046.1:c.1214A= XP_011515348.1:p.Glu405=
XR_928335.1:n.1351A=
XM_017013460.1:c.335A= XP_016868949.1:p.Glu112=
XM_017013462.2:c.335A= XP_016868951.1:p.Glu112=
XM_024447163.1:c.968A= XP_024302931.1:p.Glu323=
XM_024447164.1:c.968A= XP_024302932.1:p.Glu323=
XM_024447165.1:c.335A= XP_024302933.1:p.Glu112=
NM_002485.5:c.1214A= MANE Select NP_002476.2:p.Glu405=
NM_001024688.3:c.968A= NP_001019859.1:p.Glu323=