Canonical Allele Identifier: CA1801505378
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89970411A= , CM000670.2:g.89970411A= GRCh38
NC_000008.10:g.90982639A= , CM000670.1:g.90982639A= GRCh37
NC_000008.9:g.91051815A= NCBI36
NG_008860.1:g.19261T= , LRG_158:g.19261T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2151T=
ENST00000517337.2:c.603T= ENSP00000429971.2:p.Pro201=
ENST00000523444.2:c.603T= ENSP00000428252.2:p.Pro201=
ENST00000697292.1:c.849T= ENSP00000513229.1:p.Pro283=
ENST00000697293.1:c.849T= ENSP00000513230.1:p.Pro283=
ENST00000697294.1:c.*460T= ENSP00000513231.1:n.*460T=
ENST00000697295.1:c.*158T= ENSP00000513232.1:n.*158T=
ENST00000697296.1:c.*517T= ENSP00000513233.1:n.*517T=
ENST00000697297.1:n.2634T=
ENST00000697298.1:c.603T= ENSP00000513234.1:p.Pro201=
ENST00000697299.1:c.603T= ENSP00000513235.1:p.Pro201=
ENST00000697300.1:c.*453T= ENSP00000513236.1:n.*453T=
ENST00000697301.1:c.*370T= ENSP00000513237.1:n.*370T=
ENST00000697302.1:c.*370T= ENSP00000513238.1:n.*370T=
ENST00000697303.1:c.*453T= ENSP00000513239.1:n.*453T=
ENST00000697304.1:c.585-5904T= ENSP00000513240.1:n.585-5904T=
ENST00000697306.1:c.480+10323T= ENSP00000513241.1:n.480+10323T=
ENST00000697307.1:c.849T= ENSP00000513242.1:p.Pro283=
ENST00000697308.1:c.849T= ENSP00000513243.1:p.Pro283=
ENST00000697309.1:c.849T= ENSP00000513244.1:p.Pro283=
ENST00000697310.1:c.849T= ENSP00000513245.1:p.Pro283=
ENST00000697311.1:c.849T= ENSP00000513246.1:p.Pro283=
ENST00000697312.1:c.*247T= ENSP00000513247.1:n.*247T=
ENST00000697313.1:n.2640T=
ENST00000697314.1:n.2640T=
ENST00000697315.1:c.849T= ENSP00000513248.1:p.Pro283=
ENST00000697316.1:n.970T=
ENST00000697317.1:n.959T=
ENST00000697318.1:n.961T=
ENST00000265433.8:c.849T= MANE Select ENSP00000265433.4:p.Pro283=
ENST00000265433.7:c.849T= ENSP00000265433.3:p.Pro283=
ENST00000396252.6:c.*722T= ENSP00000379551.2:n.*722T=
ENST00000409330.5:c.603T= ENSP00000386924.1:p.Pro201=
NM_001024688.2:c.603T= NP_001019859.1:p.Pro201=
NM_002485.4:c.849T= , LRG_158t1:c.849T= NP_002476.2:p.Pro283=
XM_011517044.1:c.825T= XP_011515346.1:p.Pro275=
XM_011517045.1:c.603T= XP_011515347.1:p.Pro201=
XM_011517046.1:c.849T= XP_011515348.1:p.Pro283=
XR_928335.1:n.986T=
XM_017013460.1:c.-31T= XP_016868949.1:n.-31T=
XM_017013462.2:c.-31T= XP_016868951.1:n.-31T=
XM_024447163.1:c.603T= XP_024302931.1:p.Pro201=
XM_024447164.1:c.603T= XP_024302932.1:p.Pro201=
XM_024447165.1:c.-31T= XP_024302933.1:n.-31T=
NM_002485.5:c.849T= MANE Select NP_002476.2:p.Pro283=
NM_001024688.3:c.603T= NP_001019859.1:p.Pro201=