Canonical Allele Identifier: CA1801422821
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953359T= , CM000670.2:g.89953359T= GRCh38
NC_000008.10:g.90965587T= , CM000670.1:g.90965587T= GRCh37
NC_000008.9:g.91034763T= NCBI36
NG_008860.1:g.36313A= , LRG_158:g.36313A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3032A=
ENST00000517337.2:c.1484A= ENSP00000429971.2:p.Asp495=
ENST00000523444.2:c.1484A= ENSP00000428252.2:p.Asp495=
ENST00000697292.1:c.1730A= ENSP00000513229.1:p.Asp577=
ENST00000697293.1:c.1730A= ENSP00000513230.1:p.Asp577=
ENST00000697294.1:c.*1341A= ENSP00000513231.1:n.*1341A=
ENST00000697295.1:c.*1039A= ENSP00000513232.1:n.*1039A=
ENST00000697296.1:c.*1398A= ENSP00000513233.1:n.*1398A=
ENST00000697297.1:n.3515A=
ENST00000697298.1:c.1484A= ENSP00000513234.1:p.Asp495=
ENST00000697299.1:c.1484A= ENSP00000513235.1:p.Asp495=
ENST00000697300.1:c.*1334A= ENSP00000513236.1:n.*1334A=
ENST00000697301.1:c.*1251A= ENSP00000513237.1:n.*1251A=
ENST00000697302.1:c.*1251A= ENSP00000513238.1:n.*1251A=
ENST00000697303.1:c.*1334A= ENSP00000513239.1:n.*1334A=
ENST00000697304.1:c.1418A= ENSP00000513240.1:p.Asp473=
ENST00000697306.1:c.*730A= ENSP00000513241.1:n.*730A=
ENST00000697307.1:c.1730A= ENSP00000513242.1:p.Asp577=
ENST00000697308.1:c.1730A= ENSP00000513243.1:p.Asp577=
ENST00000697309.1:c.1730A= ENSP00000513244.1:p.Asp577=
ENST00000697310.1:c.1730A= ENSP00000513245.1:p.Asp577=
ENST00000697311.1:c.1730A= ENSP00000513246.1:p.Asp577=
ENST00000697312.1:c.*1128A= ENSP00000513247.1:n.*1128A=
ENST00000697313.1:n.2687+17005A=
ENST00000697314.1:n.3521A=
ENST00000697315.1:c.1730A= ENSP00000513248.1:p.Asp577=
ENST00000697316.1:n.1851A=
ENST00000697317.1:n.1840A=
ENST00000697318.1:n.1842A=
ENST00000265433.8:c.1730A= MANE Select ENSP00000265433.4:p.Asp577=
ENST00000265433.7:c.1730A= ENSP00000265433.3:p.Asp577=
ENST00000396252.6:c.*1603A= ENSP00000379551.2:n.*1603A=
ENST00000409330.5:c.1484A= ENSP00000386924.1:p.Asp495=
NM_001024688.2:c.1484A= NP_001019859.1:p.Asp495=
NM_002485.4:c.1730A= , LRG_158t1:c.1730A= NP_002476.2:p.Asp577=
XM_011517044.1:c.1706A= XP_011515346.1:p.Asp569=
XM_011517045.1:c.1484A= XP_011515347.1:p.Asp495=
XR_928335.1:n.1869A=
XM_017013460.1:c.851A= XP_016868949.1:p.Asp284=
XM_017013462.2:c.851A= XP_016868951.1:p.Asp284=
XM_024447163.1:c.1484A= XP_024302931.1:p.Asp495=
XM_024447164.1:c.1484A= XP_024302932.1:p.Asp495=
XM_024447165.1:c.851A= XP_024302933.1:p.Asp284=
NM_002485.5:c.1730A= MANE Select NP_002476.2:p.Asp577=
NM_001024688.3:c.1484A= NP_001019859.1:p.Asp495=