Canonical Allele Identifier: CA1801415422
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89937063G= , CM000670.2:g.89937063G= GRCh38
NC_000008.10:g.90949291G= , CM000670.1:g.90949291G= GRCh37
NC_000008.9:g.91018467G= NCBI36
NG_008860.1:g.52609C= , LRG_158:g.52609C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474821.2:n.3617C=
ENST00000494804.2:n.3499C=
ENST00000517337.2:c.1951C= ENSP00000429971.2:p.His651=
ENST00000523444.2:c.1951C= ENSP00000428252.2:p.His651=
ENST00000697292.1:c.2197C= ENSP00000513229.1:p.His733=
ENST00000697293.1:c.2248C= ENSP00000513230.1:p.His750=
ENST00000697294.1:c.*1808C= ENSP00000513231.1:n.*1808C=
ENST00000697295.1:c.*1506C= ENSP00000513232.1:n.*1506C=
ENST00000697296.1:c.*1865C= ENSP00000513233.1:n.*1865C=
ENST00000697297.1:n.3982C=
ENST00000697298.1:c.1951C= ENSP00000513234.1:p.His651=
ENST00000697299.1:c.1951C= ENSP00000513235.1:p.His651=
ENST00000697300.1:c.*1801C= ENSP00000513236.1:n.*1801C=
ENST00000697301.1:c.*1718C= ENSP00000513237.1:n.*1718C=
ENST00000697302.1:c.*1718C= ENSP00000513238.1:n.*1718C=
ENST00000697303.1:c.*1801C= ENSP00000513239.1:n.*1801C=
ENST00000697304.1:c.1885C= ENSP00000513240.1:p.His629=
ENST00000697305.1:n.2464C=
ENST00000697306.1:c.*2748C= ENSP00000513241.1:n.*2748C=
ENST00000697307.1:c.1972C= ENSP00000513242.1:p.His658=
ENST00000697308.1:c.2128C= ENSP00000513243.1:p.His710=
ENST00000697309.1:c.2185-1451C= ENSP00000513244.1:n.2185-1451C=
ENST00000697310.1:c.2197C= ENSP00000513245.1:p.His733=
ENST00000697311.1:c.*462C= ENSP00000513246.1:n.*462C=
ENST00000697312.1:c.*1650C= ENSP00000513247.1:n.*1650C=
ENST00000697313.1:n.2688-1451C=
ENST00000697314.1:n.3637-1451C=
ENST00000697315.1:c.*101C= ENSP00000513248.1:n.*101C=
ENST00000697316.1:n.2318C=
ENST00000265433.8:c.2197C= MANE Select ENSP00000265433.4:p.His733=
ENST00000265433.7:c.2197C= ENSP00000265433.3:p.His733=
ENST00000396252.6:c.*2070C= ENSP00000379551.2:n.*2070C=
ENST00000409330.5:c.1951C= ENSP00000386924.1:p.His651=
ENST00000474821.1:n.285C=
ENST00000613033.1:c.307C= ENSP00000484487.1:p.His103=
NM_001024688.2:c.1951C= NP_001019859.1:p.His651=
NM_002485.4:c.2197C= , LRG_158t1:c.2197C= NP_002476.2:p.His733=
XM_011517044.1:c.2173C= XP_011515346.1:p.His725=
XM_011517045.1:c.1951C= XP_011515347.1:p.His651=
XM_017013460.1:c.1318C= XP_016868949.1:p.His440=
XM_017013462.2:c.1318C= XP_016868951.1:p.His440=
XM_024447163.1:c.1951C= XP_024302931.1:p.His651=
XM_024447164.1:c.1951C= XP_024302932.1:p.His651=
XM_024447165.1:c.1318C= XP_024302933.1:p.His440=
NM_002485.5:c.2197C= MANE Select NP_002476.2:p.His733=
NM_001024688.3:c.1951C= NP_001019859.1:p.His651=