Canonical Allele Identifier: CA1801420293
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89947870T= , CM000670.2:g.89947870T= GRCh38
NC_000008.10:g.90960098T= , CM000670.1:g.90960098T= GRCh37
NC_000008.9:g.91029274T= NCBI36
NG_008860.1:g.41802A= , LRG_158:g.41802A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3170A=
ENST00000517337.2:c.1622A= ENSP00000429971.2:p.Lys541=
ENST00000523444.2:c.1622A= ENSP00000428252.2:p.Lys541=
ENST00000697292.1:c.1868A= ENSP00000513229.1:p.Lys623=
ENST00000697293.1:c.1868A= ENSP00000513230.1:p.Lys623=
ENST00000697294.1:c.*1479A= ENSP00000513231.1:n.*1479A=
ENST00000697295.1:c.*1177A= ENSP00000513232.1:n.*1177A=
ENST00000697296.1:c.*1536A= ENSP00000513233.1:n.*1536A=
ENST00000697297.1:n.3653A=
ENST00000697298.1:c.1622A= ENSP00000513234.1:p.Lys541=
ENST00000697299.1:c.1622A= ENSP00000513235.1:p.Lys541=
ENST00000697300.1:c.*1472A= ENSP00000513236.1:n.*1472A=
ENST00000697301.1:c.*1389A= ENSP00000513237.1:n.*1389A=
ENST00000697302.1:c.*1389A= ENSP00000513238.1:n.*1389A=
ENST00000697303.1:c.*1472A= ENSP00000513239.1:n.*1472A=
ENST00000697304.1:c.1556A= ENSP00000513240.1:p.Lys519=
ENST00000697306.1:c.*891A= ENSP00000513241.1:n.*891A=
ENST00000697307.1:c.1846-4504A= ENSP00000513242.1:n.1846-4504A=
ENST00000697308.1:c.1846-1575A= ENSP00000513243.1:n.1846-1575A=
ENST00000697309.1:c.1868A= ENSP00000513244.1:p.Lys623=
ENST00000697310.1:c.1868A= ENSP00000513245.1:p.Lys623=
ENST00000697311.1:c.1868A= ENSP00000513246.1:p.Lys623=
ENST00000697312.1:c.*1266A= ENSP00000513247.1:n.*1266A=
ENST00000697313.1:n.2688-12258A=
ENST00000697314.1:n.3636+5374A=
ENST00000697315.1:c.1868A= ENSP00000513248.1:p.Lys623=
ENST00000697316.1:n.1989A=
ENST00000697317.1:n.1978A=
ENST00000265433.8:c.1868A= MANE Select ENSP00000265433.4:p.Lys623=
ENST00000265433.7:c.1868A= ENSP00000265433.3:p.Lys623=
ENST00000396252.6:c.*1741A= ENSP00000379551.2:n.*1741A=
ENST00000409330.5:c.1622A= ENSP00000386924.1:p.Lys541=
ENST00000613033.1:c.134A= ENSP00000484487.1:p.Lys45=
NM_001024688.2:c.1622A= NP_001019859.1:p.Lys541=
NM_002485.4:c.1868A= , LRG_158t1:c.1868A= NP_002476.2:p.Lys623=
XM_011517044.1:c.1844A= XP_011515346.1:p.Lys615=
XM_011517045.1:c.1622A= XP_011515347.1:p.Lys541=
XR_928335.1:n.2007A=
XM_017013460.1:c.989A= XP_016868949.1:p.Lys330=
XM_017013462.2:c.989A= XP_016868951.1:p.Lys330=
XM_024447163.1:c.1622A= XP_024302931.1:p.Lys541=
XM_024447164.1:c.1622A= XP_024302932.1:p.Lys541=
XM_024447165.1:c.989A= XP_024302933.1:p.Lys330=
NM_002485.5:c.1868A= MANE Select NP_002476.2:p.Lys623=
NM_001024688.3:c.1622A= NP_001019859.1:p.Lys541=