Canonical Allele Identifier: CA1801422865
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953431A= , CM000670.2:g.89953431A= GRCh38
NC_000008.10:g.90965659A= , CM000670.1:g.90965659A= GRCh37
NC_000008.9:g.91034835A= NCBI36
NG_008860.1:g.36241T= , LRG_158:g.36241T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2960T=
ENST00000517337.2:c.1412T= ENSP00000429971.2:p.Met471=
ENST00000523444.2:c.1412T= ENSP00000428252.2:p.Met471=
ENST00000697292.1:c.1658T= ENSP00000513229.1:p.Met553=
ENST00000697293.1:c.1658T= ENSP00000513230.1:p.Met553=
ENST00000697294.1:c.*1269T= ENSP00000513231.1:n.*1269T=
ENST00000697295.1:c.*967T= ENSP00000513232.1:n.*967T=
ENST00000697296.1:c.*1326T= ENSP00000513233.1:n.*1326T=
ENST00000697297.1:n.3443T=
ENST00000697298.1:c.1412T= ENSP00000513234.1:p.Met471=
ENST00000697299.1:c.1412T= ENSP00000513235.1:p.Met471=
ENST00000697300.1:c.*1262T= ENSP00000513236.1:n.*1262T=
ENST00000697301.1:c.*1179T= ENSP00000513237.1:n.*1179T=
ENST00000697302.1:c.*1179T= ENSP00000513238.1:n.*1179T=
ENST00000697303.1:c.*1262T= ENSP00000513239.1:n.*1262T=
ENST00000697304.1:c.1346T= ENSP00000513240.1:p.Met449=
ENST00000697306.1:c.*658T= ENSP00000513241.1:n.*658T=
ENST00000697307.1:c.1658T= ENSP00000513242.1:p.Met553=
ENST00000697308.1:c.1658T= ENSP00000513243.1:p.Met553=
ENST00000697309.1:c.1658T= ENSP00000513244.1:p.Met553=
ENST00000697310.1:c.1658T= ENSP00000513245.1:p.Met553=
ENST00000697311.1:c.1658T= ENSP00000513246.1:p.Met553=
ENST00000697312.1:c.*1056T= ENSP00000513247.1:n.*1056T=
ENST00000697313.1:n.2687+16933T=
ENST00000697314.1:n.3449T=
ENST00000697315.1:c.1658T= ENSP00000513248.1:p.Met553=
ENST00000697316.1:n.1779T=
ENST00000697317.1:n.1768T=
ENST00000697318.1:n.1770T=
ENST00000265433.8:c.1658T= MANE Select ENSP00000265433.4:p.Met553=
ENST00000265433.7:c.1658T= ENSP00000265433.3:p.Met553=
ENST00000396252.6:c.*1531T= ENSP00000379551.2:n.*1531T=
ENST00000409330.5:c.1412T= ENSP00000386924.1:p.Met471=
NM_001024688.2:c.1412T= NP_001019859.1:p.Met471=
NM_002485.4:c.1658T= , LRG_158t1:c.1658T= NP_002476.2:p.Met553=
XM_011517044.1:c.1634T= XP_011515346.1:p.Met545=
XM_011517045.1:c.1412T= XP_011515347.1:p.Met471=
XR_928335.1:n.1797T=
XM_017013460.1:c.779T= XP_016868949.1:p.Met260=
XM_017013462.2:c.779T= XP_016868951.1:p.Met260=
XM_024447163.1:c.1412T= XP_024302931.1:p.Met471=
XM_024447164.1:c.1412T= XP_024302932.1:p.Met471=
XM_024447165.1:c.779T= XP_024302933.1:p.Met260=
NM_002485.5:c.1658T= MANE Select NP_002476.2:p.Met553=
NM_001024688.3:c.1412T= NP_001019859.1:p.Met471=