Canonical Allele Identifier: CA1801516733
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89978265A= , CM000670.2:g.89978265A= GRCh38
NC_000008.10:g.90990493A= , CM000670.1:g.90990493A= GRCh37
NC_000008.9:g.91059669A= NCBI36
NG_008860.1:g.11407T= , LRG_158:g.11407T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1841T=
ENST00000517337.2:c.293T= ENSP00000429971.2:p.Phe98=
ENST00000523444.2:c.293T= ENSP00000428252.2:p.Phe98=
ENST00000697292.1:c.539T= ENSP00000513229.1:p.Phe180=
ENST00000697293.1:c.539T= ENSP00000513230.1:p.Phe180=
ENST00000697294.1:c.*150T= ENSP00000513231.1:n.*150T=
ENST00000697295.1:c.37+6260T= ENSP00000513232.1:n.37+6260T=
ENST00000697296.1:c.*207T= ENSP00000513233.1:n.*207T=
ENST00000697297.1:n.2324T=
ENST00000697298.1:c.293T= ENSP00000513234.1:p.Phe98=
ENST00000697299.1:c.293T= ENSP00000513235.1:p.Phe98=
ENST00000697300.1:c.*143T= ENSP00000513236.1:n.*143T=
ENST00000697301.1:c.*60T= ENSP00000513237.1:n.*60T=
ENST00000697302.1:c.*60T= ENSP00000513238.1:n.*60T=
ENST00000697303.1:c.*143T= ENSP00000513239.1:n.*143T=
ENST00000697304.1:c.539T= ENSP00000513240.1:p.Phe180=
ENST00000697306.1:c.480+2469T= ENSP00000513241.1:n.480+2469T=
ENST00000697307.1:c.539T= ENSP00000513242.1:p.Phe180=
ENST00000697308.1:c.539T= ENSP00000513243.1:p.Phe180=
ENST00000697309.1:c.539T= ENSP00000513244.1:p.Phe180=
ENST00000697310.1:c.539T= ENSP00000513245.1:p.Phe180=
ENST00000697311.1:c.539T= ENSP00000513246.1:p.Phe180=
ENST00000697312.1:c.480+2469T= ENSP00000513247.1:n.480+2469T=
ENST00000697313.1:n.2330T=
ENST00000697314.1:n.2330T=
ENST00000697315.1:c.539T= ENSP00000513248.1:p.Phe180=
ENST00000697316.1:n.660T=
ENST00000697317.1:n.649T=
ENST00000697318.1:n.651T=
ENST00000265433.8:c.539T= MANE Select ENSP00000265433.4:p.Phe180=
ENST00000265433.7:c.539T= ENSP00000265433.3:p.Phe180=
ENST00000396252.6:c.*412T= ENSP00000379551.2:n.*412T=
ENST00000409330.5:c.293T= ENSP00000386924.1:p.Phe98=
ENST00000517772.5:c.293T= ENSP00000428717.1:p.Phe98=
ENST00000519426.5:c.320+3110T= ENSP00000430983.1:n.320+3110T=
NM_001024688.2:c.293T= NP_001019859.1:p.Phe98=
NM_002485.4:c.539T= , LRG_158t1:c.539T= NP_002476.2:p.Phe180=
XM_011517044.1:c.515T= XP_011515346.1:p.Phe172=
XM_011517045.1:c.293T= XP_011515347.1:p.Phe98=
XM_011517046.1:c.539T= XP_011515348.1:p.Phe180=
XR_928335.1:n.676T=
XM_017013460.1:c.-341T= XP_016868949.1:n.-341T=
XM_017013462.2:c.-296+2469T= XP_016868951.1:n.-296+2469T=
XM_024447163.1:c.293T= XP_024302931.1:p.Phe98=
XM_024447164.1:c.293T= XP_024302932.1:p.Phe98=
XM_024447165.1:c.-341T= XP_024302933.1:n.-341T=
NM_002485.5:c.539T= MANE Select NP_002476.2:p.Phe180=
NM_001024688.3:c.293T= NP_001019859.1:p.Phe98=