Canonical Allele Identifier: CA1801516827
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89978287T= , CM000670.2:g.89978287T= GRCh38
NC_000008.10:g.90990515T= , CM000670.1:g.90990515T= GRCh37
NC_000008.9:g.91059691T= NCBI36
NG_008860.1:g.11385A= , LRG_158:g.11385A=

Transcript Alleles

HGVS Amino-acid change
ENST00000494804.2:n.1819A=
ENST00000517337.2:c.271A= ENSP00000429971.2:p.Lys91=
ENST00000523444.2:c.271A= ENSP00000428252.2:p.Lys91=
ENST00000697292.1:c.517A= ENSP00000513229.1:p.Lys173=
ENST00000697293.1:c.517A= ENSP00000513230.1:p.Lys173=
ENST00000697294.1:c.*128A= ENSP00000513231.1:n.*128A=
ENST00000697295.1:c.37+6238A= ENSP00000513232.1:n.37+6238A=
ENST00000697296.1:c.*185A= ENSP00000513233.1:n.*185A=
ENST00000697297.1:n.2302A=
ENST00000697298.1:c.271A= ENSP00000513234.1:p.Lys91=
ENST00000697299.1:c.271A= ENSP00000513235.1:p.Lys91=
ENST00000697300.1:c.*121A= ENSP00000513236.1:n.*121A=
ENST00000697301.1:c.*38A= ENSP00000513237.1:n.*38A=
ENST00000697302.1:c.*38A= ENSP00000513238.1:n.*38A=
ENST00000697303.1:c.*121A= ENSP00000513239.1:n.*121A=
ENST00000697304.1:c.517A= ENSP00000513240.1:p.Lys173=
ENST00000697306.1:c.480+2447A= ENSP00000513241.1:n.480+2447A=
ENST00000697307.1:c.517A= ENSP00000513242.1:p.Lys173=
ENST00000697308.1:c.517A= ENSP00000513243.1:p.Lys173=
ENST00000697309.1:c.517A= ENSP00000513244.1:p.Lys173=
ENST00000697310.1:c.517A= ENSP00000513245.1:p.Lys173=
ENST00000697311.1:c.517A= ENSP00000513246.1:p.Lys173=
ENST00000697312.1:c.480+2447A= ENSP00000513247.1:n.480+2447A=
ENST00000697313.1:n.2308A=
ENST00000697314.1:n.2308A=
ENST00000697315.1:c.517A= ENSP00000513248.1:p.Lys173=
ENST00000697316.1:n.638A=
ENST00000697317.1:n.627A=
ENST00000697318.1:n.629A=
ENST00000265433.8:c.517A= MANE Select ENSP00000265433.4:p.Lys173=
ENST00000265433.7:c.517A= ENSP00000265433.3:p.Lys173=
ENST00000396252.6:c.*390A= ENSP00000379551.2:n.*390A=
ENST00000409330.5:c.271A= ENSP00000386924.1:p.Lys91=
ENST00000517337.1:c.271A= ENSP00000429971.1:p.Lys91=
ENST00000517772.5:c.271A= ENSP00000428717.1:p.Lys91=
ENST00000519426.5:c.320+3088A= ENSP00000430983.1:n.320+3088A=
ENST00000523444.1:c.*349A= ENSP00000428252.1:n.*349A=
NM_001024688.2:c.271A= NP_001019859.1:p.Lys91=
NM_002485.4:c.517A= , LRG_158t1:c.517A= NP_002476.2:p.Lys173=
XM_011517044.1:c.493A= XP_011515346.1:p.Lys165=
XM_011517045.1:c.271A= XP_011515347.1:p.Lys91=
XM_011517046.1:c.517A= XP_011515348.1:p.Lys173=
XR_928335.1:n.654A=
XM_017013460.1:c.-363A= XP_016868949.1:n.-363A=
XM_017013462.2:c.-296+2447A= XP_016868951.1:n.-296+2447A=
XM_024447163.1:c.271A= XP_024302931.1:p.Lys91=
XM_024447164.1:c.271A= XP_024302932.1:p.Lys91=
XM_024447165.1:c.-363A= XP_024302933.1:n.-363A=
NM_002485.5:c.517A= MANE Select NP_002476.2:p.Lys173=
NM_001024688.3:c.271A= NP_001019859.1:p.Lys91=