Canonical Allele Identifier: CA1801470849
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89984232T= , CM000670.2:g.89984232T= GRCh38
NC_000008.10:g.90996460T= , CM000670.1:g.90996460T= GRCh37
NC_000008.9:g.91065636T= NCBI36
NG_008860.1:g.5440A= , LRG_158:g.5440A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.141+293A=
ENST00000517337.2:c.-284A= ENSP00000429971.2:n.-284A=
ENST00000523444.2:c.-260+293A= ENSP00000428252.2:n.-260+293A=
ENST00000697292.1:c.37+293A= ENSP00000513229.1:n.37+293A=
ENST00000697293.1:c.37+293A= ENSP00000513230.1:n.37+293A=
ENST00000697294.1:c.37+293A= ENSP00000513231.1:n.37+293A=
ENST00000697295.1:c.37+293A= ENSP00000513232.1:n.37+293A=
ENST00000697296.1:c.37+293A= ENSP00000513233.1:n.37+293A=
ENST00000697297.1:n.143+293A=
ENST00000697298.1:c.-442-173A= ENSP00000513234.1:n.-442-173A=
ENST00000697299.1:c.-76+293A= ENSP00000513235.1:n.-76+293A=
ENST00000697300.1:c.-260+293A= ENSP00000513236.1:n.-260+293A=
ENST00000697301.1:c.-260+293A= ENSP00000513237.1:n.-260+293A=
ENST00000697302.1:c.37+293A= ENSP00000513238.1:n.37+293A=
ENST00000697303.1:c.37+293A= ENSP00000513239.1:n.37+293A=
ENST00000697304.1:c.37+293A= ENSP00000513240.1:n.37+293A=
ENST00000697306.1:c.37+293A= ENSP00000513241.1:n.37+293A=
ENST00000697307.1:c.37+293A= ENSP00000513242.1:n.37+293A=
ENST00000697308.1:c.37+293A= ENSP00000513243.1:n.37+293A=
ENST00000697309.1:c.37+293A= ENSP00000513244.1:n.37+293A=
ENST00000697310.1:c.37+293A= ENSP00000513245.1:n.37+293A=
ENST00000697311.1:c.37+293A= ENSP00000513246.1:n.37+293A=
ENST00000697312.1:c.37+293A= ENSP00000513247.1:n.37+293A=
ENST00000697313.1:n.149+293A=
ENST00000697314.1:n.149+293A=
ENST00000697315.1:c.37+293A= ENSP00000513248.1:n.37+293A=
ENST00000697316.1:n.158+293A=
ENST00000697317.1:n.147+293A=
ENST00000697318.1:n.149+293A=
ENST00000265433.8:c.37+293A= MANE Select ENSP00000265433.4:n.37+293A=
ENST00000265433.7:c.37+293A= ENSP00000265433.3:n.37+293A=
ENST00000396252.6:c.37+293A= ENSP00000379551.2:n.37+293A=
ENST00000409330.5:c.-234A= ENSP00000386924.1:n.-234A=
ENST00000494804.1:n.141+293A=
ENST00000517337.1:c.-284A= ENSP00000429971.1:n.-284A=
ENST00000519426.5:c.37+293A= ENSP00000430983.1:n.37+293A=
ENST00000523444.1:c.37+293A= ENSP00000428252.1:n.37+293A=
NM_001024688.2:c.-260+293A= NP_001019859.1:n.-260+293A=
NM_002485.4:c.37+293A= , LRG_158t1:c.37+293A= NP_002476.2:n.37+293A=
XM_011517045.1:c.-284A= XP_011515347.1:n.-284A=
XM_011517046.1:c.37+293A= XP_011515348.1:n.37+293A=
XR_928335.1:n.174+293A=
XM_017013460.1:c.-983+293A= XP_016868949.1:n.-983+293A=
XM_017013462.2:c.-789+293A= XP_016868951.1:n.-789+293A=
XM_024447163.1:c.-234A= XP_024302931.1:n.-234A=
XM_024447165.1:c.-933+293A= XP_024302933.1:n.-933+293A=
NM_002485.5:c.37+293A= MANE Select NP_002476.2:n.37+293A=
NM_001024688.3:c.-260+293A= NP_001019859.1:n.-260+293A=