Canonical Allele Identifier: CA1801507883
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89971333G= , CM000670.2:g.89971333G= GRCh38
NC_000008.10:g.90983561G= , CM000670.1:g.90983561G= GRCh37
NC_000008.9:g.91052737G= NCBI36
NG_008860.1:g.18339C= , LRG_158:g.18339C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1887-43C=
ENST00000517337.2:c.339-43C= ENSP00000429971.2:n.339-43C=
ENST00000523444.2:c.339-43C= ENSP00000428252.2:n.339-43C=
ENST00000697292.1:c.585-43C= ENSP00000513229.1:n.585-43C=
ENST00000697293.1:c.585-43C= ENSP00000513230.1:n.585-43C=
ENST00000697294.1:c.*196-43C= ENSP00000513231.1:n.*196-43C=
ENST00000697295.1:c.38-43C= ENSP00000513232.1:n.38-43C=
ENST00000697296.1:c.*253-43C= ENSP00000513233.1:n.*253-43C=
ENST00000697297.1:n.2370-43C=
ENST00000697298.1:c.339-43C= ENSP00000513234.1:n.339-43C=
ENST00000697299.1:c.339-43C= ENSP00000513235.1:n.339-43C=
ENST00000697300.1:c.*189-43C= ENSP00000513236.1:n.*189-43C=
ENST00000697301.1:c.*106-43C= ENSP00000513237.1:n.*106-43C=
ENST00000697302.1:c.*106-43C= ENSP00000513238.1:n.*106-43C=
ENST00000697303.1:c.*189-43C= ENSP00000513239.1:n.*189-43C=
ENST00000697304.1:c.585-6826C= ENSP00000513240.1:n.585-6826C=
ENST00000697306.1:c.480+9401C= ENSP00000513241.1:n.480+9401C=
ENST00000697307.1:c.585-43C= ENSP00000513242.1:n.585-43C=
ENST00000697308.1:c.585-43C= ENSP00000513243.1:n.585-43C=
ENST00000697309.1:c.585-43C= ENSP00000513244.1:n.585-43C=
ENST00000697310.1:c.585-43C= ENSP00000513245.1:n.585-43C=
ENST00000697311.1:c.585-43C= ENSP00000513246.1:n.585-43C=
ENST00000697312.1:c.481-43C= ENSP00000513247.1:n.481-43C=
ENST00000697313.1:n.2376-43C=
ENST00000697314.1:n.2376-43C=
ENST00000697315.1:c.585-43C= ENSP00000513248.1:n.585-43C=
ENST00000697316.1:n.706-43C=
ENST00000697317.1:n.695-43C=
ENST00000697318.1:n.697-43C=
ENST00000265433.8:c.585-43C= MANE Select ENSP00000265433.4:n.585-43C=
ENST00000265433.7:c.585-43C= ENSP00000265433.3:n.585-43C=
ENST00000396252.6:c.*458-43C= ENSP00000379551.2:n.*458-43C=
ENST00000409330.5:c.339-43C= ENSP00000386924.1:n.339-43C=
ENST00000517772.5:c.339-43C= ENSP00000428717.1:n.339-43C=
ENST00000519426.5:c.321-43C= ENSP00000430983.1:n.321-43C=
NM_001024688.2:c.339-43C= NP_001019859.1:n.339-43C=
NM_002485.4:c.585-43C= , LRG_158t1:c.585-43C= NP_002476.2:n.585-43C=
XM_011517044.1:c.561-43C= XP_011515346.1:n.561-43C=
XM_011517045.1:c.339-43C= XP_011515347.1:n.339-43C=
XM_011517046.1:c.585-43C= XP_011515348.1:n.585-43C=
XR_928335.1:n.722-43C=
XM_017013460.1:c.-295-43C= XP_016868949.1:n.-295-43C=
XM_017013462.2:c.-295-43C= XP_016868951.1:n.-295-43C=
XM_024447163.1:c.339-43C= XP_024302931.1:n.339-43C=
XM_024447164.1:c.339-43C= XP_024302932.1:n.339-43C=
XM_024447165.1:c.-295-43C= XP_024302933.1:n.-295-43C=
NM_002485.5:c.585-43C= MANE Select NP_002476.2:n.585-43C=
NM_001024688.3:c.339-43C= NP_001019859.1:n.339-43C=