Canonical Allele Identifier: CA1801505204
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89970377C= , CM000670.2:g.89970377C= GRCh38
NC_000008.10:g.90982605C= , CM000670.1:g.90982605C= GRCh37
NC_000008.9:g.91051781C= NCBI36
NG_008860.1:g.19295G= , LRG_158:g.19295G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2185G=
ENST00000517337.2:c.637G= ENSP00000429971.2:p.Asp213=
ENST00000523444.2:c.637G= ENSP00000428252.2:p.Asp213=
ENST00000697292.1:c.883G= ENSP00000513229.1:p.Asp295=
ENST00000697293.1:c.883G= ENSP00000513230.1:p.Asp295=
ENST00000697294.1:c.*494G= ENSP00000513231.1:n.*494G=
ENST00000697295.1:c.*192G= ENSP00000513232.1:n.*192G=
ENST00000697296.1:c.*551G= ENSP00000513233.1:n.*551G=
ENST00000697297.1:n.2668G=
ENST00000697298.1:c.637G= ENSP00000513234.1:p.Asp213=
ENST00000697299.1:c.637G= ENSP00000513235.1:p.Asp213=
ENST00000697300.1:c.*487G= ENSP00000513236.1:n.*487G=
ENST00000697301.1:c.*404G= ENSP00000513237.1:n.*404G=
ENST00000697302.1:c.*404G= ENSP00000513238.1:n.*404G=
ENST00000697303.1:c.*487G= ENSP00000513239.1:n.*487G=
ENST00000697304.1:c.585-5870G= ENSP00000513240.1:n.585-5870G=
ENST00000697306.1:c.480+10357G= ENSP00000513241.1:n.480+10357G=
ENST00000697307.1:c.883G= ENSP00000513242.1:p.Asp295=
ENST00000697308.1:c.883G= ENSP00000513243.1:p.Asp295=
ENST00000697309.1:c.883G= ENSP00000513244.1:p.Asp295=
ENST00000697310.1:c.883G= ENSP00000513245.1:p.Asp295=
ENST00000697311.1:c.883G= ENSP00000513246.1:p.Asp295=
ENST00000697312.1:c.*281G= ENSP00000513247.1:n.*281G=
ENST00000697313.1:n.2674G=
ENST00000697314.1:n.2674G=
ENST00000697315.1:c.883G= ENSP00000513248.1:p.Asp295=
ENST00000697316.1:n.1004G=
ENST00000697317.1:n.993G=
ENST00000697318.1:n.995G=
ENST00000265433.8:c.883G= MANE Select ENSP00000265433.4:p.Asp295=
ENST00000265433.7:c.883G= ENSP00000265433.3:p.Asp295=
ENST00000396252.6:c.*756G= ENSP00000379551.2:n.*756G=
ENST00000409330.5:c.637G= ENSP00000386924.1:p.Asp213=
NM_001024688.2:c.637G= NP_001019859.1:p.Asp213=
NM_002485.4:c.883G= , LRG_158t1:c.883G= NP_002476.2:p.Asp295=
XM_011517044.1:c.859G= XP_011515346.1:p.Asp287=
XM_011517045.1:c.637G= XP_011515347.1:p.Asp213=
XM_011517046.1:c.883G= XP_011515348.1:p.Asp295=
XR_928335.1:n.1020G=
XM_017013460.1:c.4G= XP_016868949.1:p.Asp2=
XM_017013462.2:c.4G= XP_016868951.1:p.Asp2=
XM_024447163.1:c.637G= XP_024302931.1:p.Asp213=
XM_024447164.1:c.637G= XP_024302932.1:p.Asp213=
XM_024447165.1:c.4G= XP_024302933.1:p.Asp2=
NM_002485.5:c.883G= MANE Select NP_002476.2:p.Asp295=
NM_001024688.3:c.637G= NP_001019859.1:p.Asp213=