Canonical Allele Identifier: CA1801415415
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89937050T= , CM000670.2:g.89937050T= GRCh38
NC_000008.10:g.90949278T= , CM000670.1:g.90949278T= GRCh37
NC_000008.9:g.91018454T= NCBI36
NG_008860.1:g.52622A= , LRG_158:g.52622A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474821.2:n.3630A=
ENST00000494804.2:n.3512A=
ENST00000517337.2:c.1964A= ENSP00000429971.2:p.Glu655=
ENST00000523444.2:c.1964A= ENSP00000428252.2:p.Glu655=
ENST00000697292.1:c.2210A= ENSP00000513229.1:p.Glu737=
ENST00000697293.1:c.2261A= ENSP00000513230.1:p.Glu754=
ENST00000697294.1:c.*1821A= ENSP00000513231.1:n.*1821A=
ENST00000697295.1:c.*1519A= ENSP00000513232.1:n.*1519A=
ENST00000697296.1:c.*1878A= ENSP00000513233.1:n.*1878A=
ENST00000697297.1:n.3995A=
ENST00000697298.1:c.1964A= ENSP00000513234.1:p.Glu655=
ENST00000697299.1:c.1964A= ENSP00000513235.1:p.Glu655=
ENST00000697300.1:c.*1814A= ENSP00000513236.1:n.*1814A=
ENST00000697301.1:c.*1731A= ENSP00000513237.1:n.*1731A=
ENST00000697302.1:c.*1731A= ENSP00000513238.1:n.*1731A=
ENST00000697303.1:c.*1814A= ENSP00000513239.1:n.*1814A=
ENST00000697304.1:c.1898A= ENSP00000513240.1:p.Glu633=
ENST00000697305.1:n.2477A=
ENST00000697306.1:c.*2761A= ENSP00000513241.1:n.*2761A=
ENST00000697307.1:c.1985A= ENSP00000513242.1:p.Glu662=
ENST00000697308.1:c.2141A= ENSP00000513243.1:p.Glu714=
ENST00000697309.1:c.2185-1438A= ENSP00000513244.1:n.2185-1438A=
ENST00000697310.1:c.2210A= ENSP00000513245.1:p.Glu737=
ENST00000697311.1:c.*475A= ENSP00000513246.1:n.*475A=
ENST00000697312.1:c.*1663A= ENSP00000513247.1:n.*1663A=
ENST00000697313.1:n.2688-1438A=
ENST00000697314.1:n.3637-1438A=
ENST00000697315.1:c.*114A= ENSP00000513248.1:n.*114A=
ENST00000697316.1:n.2331A=
ENST00000265433.8:c.2210A= MANE Select ENSP00000265433.4:p.Glu737=
ENST00000265433.7:c.2210A= ENSP00000265433.3:p.Glu737=
ENST00000396252.6:c.*2083A= ENSP00000379551.2:n.*2083A=
ENST00000409330.5:c.1964A= ENSP00000386924.1:p.Glu655=
ENST00000474821.1:n.298A=
ENST00000613033.1:c.320A= ENSP00000484487.1:p.Glu107=
NM_001024688.2:c.1964A= NP_001019859.1:p.Glu655=
NM_002485.4:c.2210A= , LRG_158t1:c.2210A= NP_002476.2:p.Glu737=
XM_011517044.1:c.2186A= XP_011515346.1:p.Glu729=
XM_011517045.1:c.1964A= XP_011515347.1:p.Glu655=
XM_017013460.1:c.1331A= XP_016868949.1:p.Glu444=
XM_017013462.2:c.1331A= XP_016868951.1:p.Glu444=
XM_024447163.1:c.1964A= XP_024302931.1:p.Glu655=
XM_024447164.1:c.1964A= XP_024302932.1:p.Glu655=
XM_024447165.1:c.1331A= XP_024302933.1:p.Glu444=
NM_002485.5:c.2210A= MANE Select NP_002476.2:p.Glu737=
NM_001024688.3:c.1964A= NP_001019859.1:p.Glu655=