Canonical Allele Identifier: CA1801520980
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89980919A= , CM000670.2:g.89980919A= GRCh38
NC_000008.10:g.90993147A= , CM000670.1:g.90993147A= GRCh37
NC_000008.9:g.91062323A= NCBI36
NG_008860.1:g.8753T= , LRG_158:g.8753T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1623-26T=
ENST00000517337.2:c.75-26T= ENSP00000429971.2:n.75-26T=
ENST00000523444.2:c.75-26T= ENSP00000428252.2:n.75-26T=
ENST00000697292.1:c.321-26T= ENSP00000513229.1:n.321-26T=
ENST00000697293.1:c.321-26T= ENSP00000513230.1:n.321-26T=
ENST00000697294.1:c.321-67T= ENSP00000513231.1:n.321-67T=
ENST00000697295.1:c.37+3606T= ENSP00000513232.1:n.37+3606T=
ENST00000697296.1:c.172-26T= ENSP00000513233.1:n.172-26T=
ENST00000697297.1:n.2080T=
ENST00000697298.1:c.75-26T= ENSP00000513234.1:n.75-26T=
ENST00000697299.1:c.75-26T= ENSP00000513235.1:n.75-26T=
ENST00000697300.1:c.75-26T= ENSP00000513236.1:n.75-26T=
ENST00000697301.1:c.75-67T= ENSP00000513237.1:n.75-67T=
ENST00000697302.1:c.321-67T= ENSP00000513238.1:n.321-67T=
ENST00000697303.1:c.321-26T= ENSP00000513239.1:n.321-26T=
ENST00000697304.1:c.321-26T= ENSP00000513240.1:n.321-26T=
ENST00000697306.1:c.321-26T= ENSP00000513241.1:n.321-26T=
ENST00000697307.1:c.321-26T= ENSP00000513242.1:n.321-26T=
ENST00000697308.1:c.321-26T= ENSP00000513243.1:n.321-26T=
ENST00000697309.1:c.321-26T= ENSP00000513244.1:n.321-26T=
ENST00000697310.1:c.321-26T= ENSP00000513245.1:n.321-26T=
ENST00000697311.1:c.321-26T= ENSP00000513246.1:n.321-26T=
ENST00000697312.1:c.321-26T= ENSP00000513247.1:n.321-26T=
ENST00000697313.1:n.2086T=
ENST00000697314.1:n.2086T=
ENST00000697315.1:c.321-26T= ENSP00000513248.1:n.321-26T=
ENST00000697316.1:n.442-26T=
ENST00000697317.1:n.431-26T=
ENST00000697318.1:n.433-26T=
ENST00000265433.8:c.321-26T= MANE Select ENSP00000265433.4:n.321-26T=
ENST00000265433.7:c.321-26T= ENSP00000265433.3:n.321-26T=
ENST00000396252.6:c.*194-26T= ENSP00000379551.2:n.*194-26T=
ENST00000409330.5:c.75-26T= ENSP00000386924.1:n.75-26T=
ENST00000517337.1:c.75-26T= ENSP00000429971.1:n.75-26T=
ENST00000517772.5:c.75-26T= ENSP00000428717.1:n.75-26T=
ENST00000519426.5:c.320+456T= ENSP00000430983.1:n.320+456T=
ENST00000523444.1:c.*194-67T= ENSP00000428252.1:n.*194-67T=
NM_001024688.2:c.75-26T= NP_001019859.1:n.75-26T=
NM_002485.4:c.321-26T= , LRG_158t1:c.321-26T= NP_002476.2:n.321-26T=
XM_011517044.1:c.297-26T= XP_011515346.1:n.297-26T=
XM_011517045.1:c.75-26T= XP_011515347.1:n.75-26T=
XM_011517046.1:c.321-26T= XP_011515348.1:n.321-26T=
XR_928335.1:n.458-26T=
XM_017013460.1:c.-649-26T= XP_016868949.1:n.-649-26T=
XM_017013462.2:c.-455-26T= XP_016868951.1:n.-455-26T=
XM_024447163.1:c.75-26T= XP_024302931.1:n.75-26T=
XM_024447164.1:c.75-26T= XP_024302932.1:n.75-26T=
XM_024447165.1:c.-649-26T= XP_024302933.1:n.-649-26T=
NM_002485.5:c.321-26T= MANE Select NP_002476.2:n.321-26T=
NM_001024688.3:c.75-26T= NP_001019859.1:n.75-26T=