Canonical Allele Identifier: CA1801506982
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89971067C= , CM000670.2:g.89971067C= GRCh38
NC_000008.10:g.90983295C= , CM000670.1:g.90983295C= GRCh37
NC_000008.9:g.91052471C= NCBI36
NG_008860.1:g.18605G= , LRG_158:g.18605G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2004+106G=
ENST00000517337.2:c.456+106G= ENSP00000429971.2:n.456+106G=
ENST00000523444.2:c.456+106G= ENSP00000428252.2:n.456+106G=
ENST00000697292.1:c.702+106G= ENSP00000513229.1:n.702+106G=
ENST00000697293.1:c.702+106G= ENSP00000513230.1:n.702+106G=
ENST00000697294.1:c.*313+106G= ENSP00000513231.1:n.*313+106G=
ENST00000697295.1:c.*11+106G= ENSP00000513232.1:n.*11+106G=
ENST00000697296.1:c.*370+106G= ENSP00000513233.1:n.*370+106G=
ENST00000697297.1:n.2487+106G=
ENST00000697298.1:c.456+106G= ENSP00000513234.1:n.456+106G=
ENST00000697299.1:c.456+106G= ENSP00000513235.1:n.456+106G=
ENST00000697300.1:c.*306+106G= ENSP00000513236.1:n.*306+106G=
ENST00000697301.1:c.*223+106G= ENSP00000513237.1:n.*223+106G=
ENST00000697302.1:c.*223+106G= ENSP00000513238.1:n.*223+106G=
ENST00000697303.1:c.*306+106G= ENSP00000513239.1:n.*306+106G=
ENST00000697304.1:c.585-6560G= ENSP00000513240.1:n.585-6560G=
ENST00000697306.1:c.480+9667G= ENSP00000513241.1:n.480+9667G=
ENST00000697307.1:c.702+106G= ENSP00000513242.1:n.702+106G=
ENST00000697308.1:c.702+106G= ENSP00000513243.1:n.702+106G=
ENST00000697309.1:c.702+106G= ENSP00000513244.1:n.702+106G=
ENST00000697310.1:c.702+106G= ENSP00000513245.1:n.702+106G=
ENST00000697311.1:c.702+106G= ENSP00000513246.1:n.702+106G=
ENST00000697312.1:c.*100+106G= ENSP00000513247.1:n.*100+106G=
ENST00000697313.1:n.2493+106G=
ENST00000697314.1:n.2493+106G=
ENST00000697315.1:c.702+106G= ENSP00000513248.1:n.702+106G=
ENST00000697316.1:n.823+106G=
ENST00000697317.1:n.812+106G=
ENST00000697318.1:n.814+106G=
ENST00000265433.8:c.702+106G= MANE Select ENSP00000265433.4:n.702+106G=
ENST00000265433.7:c.702+106G= ENSP00000265433.3:n.702+106G=
ENST00000396252.6:c.*575+106G= ENSP00000379551.2:n.*575+106G=
ENST00000409330.5:c.456+106G= ENSP00000386924.1:n.456+106G=
ENST00000517772.5:c.456+106G= ENSP00000428717.1:n.456+106G=
ENST00000519426.5:c.438+106G= ENSP00000430983.1:n.438+106G=
NM_001024688.2:c.456+106G= NP_001019859.1:n.456+106G=
NM_002485.4:c.702+106G= , LRG_158t1:c.702+106G= NP_002476.2:n.702+106G=
XM_011517044.1:c.678+106G= XP_011515346.1:n.678+106G=
XM_011517045.1:c.456+106G= XP_011515347.1:n.456+106G=
XM_011517046.1:c.702+106G= XP_011515348.1:n.702+106G=
XR_928335.1:n.839+106G=
XM_017013460.1:c.-178+106G= XP_016868949.1:n.-178+106G=
XM_017013462.2:c.-178+106G= XP_016868951.1:n.-178+106G=
XM_024447163.1:c.456+106G= XP_024302931.1:n.456+106G=
XM_024447164.1:c.456+106G= XP_024302932.1:n.456+106G=
XM_024447165.1:c.-178+106G= XP_024302933.1:n.-178+106G=
NM_002485.5:c.702+106G= MANE Select NP_002476.2:n.702+106G=
NM_001024688.3:c.456+106G= NP_001019859.1:n.456+106G=