Canonical Allele Identifier: CA1801469891
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89982726T= , CM000670.2:g.89982726T= GRCh38
NC_000008.10:g.90994954T= , CM000670.1:g.90994954T= GRCh37
NC_000008.9:g.91064130T= NCBI36
NG_008860.1:g.6946A= , LRG_158:g.6946A=

Transcript Alleles

HGVS Amino-acid change
ENST00000494804.2:n.271A=
ENST00000517337.2:c.-130A= ENSP00000429971.2:n.-130A=
ENST00000523444.2:c.-130A= ENSP00000428252.2:n.-130A=
ENST00000697292.1:c.167A= ENSP00000513229.1:p.Asn56=
ENST00000697293.1:c.167A= ENSP00000513230.1:p.Asn56=
ENST00000697294.1:c.167A= ENSP00000513231.1:p.Asn56=
ENST00000697295.1:c.37+1799A= ENSP00000513232.1:n.37+1799A=
ENST00000697296.1:c.167A= ENSP00000513233.1:p.Asn56=
ENST00000697297.1:n.273A=
ENST00000697298.1:c.-130A= ENSP00000513234.1:n.-130A=
ENST00000697299.1:c.-75-1203A= ENSP00000513235.1:n.-75-1203A=
ENST00000697300.1:c.-130A= ENSP00000513236.1:n.-130A=
ENST00000697301.1:c.-130A= ENSP00000513237.1:n.-130A=
ENST00000697302.1:c.167A= ENSP00000513238.1:p.Asn56=
ENST00000697303.1:c.167A= ENSP00000513239.1:p.Asn56=
ENST00000697304.1:c.167A= ENSP00000513240.1:p.Asn56=
ENST00000697306.1:c.167A= ENSP00000513241.1:p.Asn56=
ENST00000697307.1:c.167A= ENSP00000513242.1:p.Asn56=
ENST00000697308.1:c.167A= ENSP00000513243.1:p.Asn56=
ENST00000697309.1:c.167A= ENSP00000513244.1:p.Asn56=
ENST00000697310.1:c.167A= ENSP00000513245.1:p.Asn56=
ENST00000697311.1:c.167A= ENSP00000513246.1:p.Asn56=
ENST00000697312.1:c.167A= ENSP00000513247.1:p.Asn56=
ENST00000697313.1:n.279A=
ENST00000697314.1:n.279A=
ENST00000697315.1:c.167A= ENSP00000513248.1:p.Asn56=
ENST00000697316.1:n.288A=
ENST00000697317.1:n.277A=
ENST00000697318.1:n.279A=
ENST00000265433.8:c.167A= MANE Select ENSP00000265433.4:p.Asn56=
ENST00000265433.7:c.167A= ENSP00000265433.3:p.Asn56=
ENST00000396252.6:c.167A= ENSP00000379551.2:p.Asn56=
ENST00000409330.5:c.-80A= ENSP00000386924.1:n.-80A=
ENST00000494804.1:n.271A=
ENST00000517337.1:c.-130A= ENSP00000429971.1:n.-130A=
ENST00000519426.5:c.167A= ENSP00000430983.1:p.Asn56=
ENST00000523444.1:c.167A= ENSP00000428252.1:p.Asn56=
NM_001024688.2:c.-130A= NP_001019859.1:n.-130A=
NM_002485.4:c.167A= , LRG_158t1:c.167A= NP_002476.2:p.Asn56=
XM_011517044.1:c.143A= XP_011515346.1:p.Asn48=
XM_011517045.1:c.-130A= XP_011515347.1:n.-130A=
XM_011517046.1:c.167A= XP_011515348.1:p.Asn56=
XR_928335.1:n.304A=
XM_017013460.1:c.-853A= XP_016868949.1:n.-853A=
XM_017013462.2:c.-659A= XP_016868951.1:n.-659A=
XM_024447163.1:c.-80A= XP_024302931.1:n.-80A=
XM_024447165.1:c.-803A= XP_024302933.1:n.-803A=
NM_002485.5:c.167A= MANE Select NP_002476.2:p.Asn56=
NM_001024688.3:c.-130A= NP_001019859.1:n.-130A=