Canonical Allele Identifier: CA1801419487
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89946160T= , CM000670.2:g.89946160T= GRCh38
NC_000008.10:g.90958388T= , CM000670.1:g.90958388T= GRCh37
NC_000008.9:g.91027564T= NCBI36
NG_008860.1:g.43512A= , LRG_158:g.43512A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.3352A=
ENST00000517337.2:c.1804A= ENSP00000429971.2:p.Asn602=
ENST00000523444.2:c.1804A= ENSP00000428252.2:p.Asn602=
ENST00000697292.1:c.2050A= ENSP00000513229.1:p.Asn684=
ENST00000697293.1:c.2050A= ENSP00000513230.1:p.Asn684=
ENST00000697294.1:c.*1661A= ENSP00000513231.1:n.*1661A=
ENST00000697295.1:c.*1359A= ENSP00000513232.1:n.*1359A=
ENST00000697296.1:c.*1718A= ENSP00000513233.1:n.*1718A=
ENST00000697297.1:n.3835A=
ENST00000697298.1:c.1804A= ENSP00000513234.1:p.Asn602=
ENST00000697299.1:c.1804A= ENSP00000513235.1:p.Asn602=
ENST00000697300.1:c.*1654A= ENSP00000513236.1:n.*1654A=
ENST00000697301.1:c.*1571A= ENSP00000513237.1:n.*1571A=
ENST00000697302.1:c.*1571A= ENSP00000513238.1:n.*1571A=
ENST00000697303.1:c.*1654A= ENSP00000513239.1:n.*1654A=
ENST00000697304.1:c.1738A= ENSP00000513240.1:p.Asn580=
ENST00000697306.1:c.*2601A= ENSP00000513241.1:n.*2601A=
ENST00000697307.1:c.1846-2794A= ENSP00000513242.1:n.1846-2794A=
ENST00000697308.1:c.1981A= ENSP00000513243.1:p.Asn661=
ENST00000697309.1:c.2050A= ENSP00000513244.1:p.Asn684=
ENST00000697310.1:c.2050A= ENSP00000513245.1:p.Asn684=
ENST00000697311.1:c.2050A= ENSP00000513246.1:p.Asn684=
ENST00000697312.1:c.*1448A= ENSP00000513247.1:n.*1448A=
ENST00000697313.1:n.2688-10548A=
ENST00000697314.1:n.3636+7084A=
ENST00000697315.1:c.2050A= ENSP00000513248.1:p.Asn684=
ENST00000697316.1:n.2171A=
ENST00000697317.1:n.2141A=
ENST00000265433.8:c.2050A= MANE Select ENSP00000265433.4:p.Asn684=
ENST00000265433.7:c.2050A= ENSP00000265433.3:p.Asn684=
ENST00000396252.6:c.*1923A= ENSP00000379551.2:n.*1923A=
ENST00000409330.5:c.1804A= ENSP00000386924.1:p.Asn602=
ENST00000520325.1:n.466A=
ENST00000613033.1:c.180+1664A= ENSP00000484487.1:n.180+1664A=
NM_001024688.2:c.1804A= NP_001019859.1:p.Asn602=
NM_002485.4:c.2050A= , LRG_158t1:c.2050A= NP_002476.2:p.Asn684=
XM_011517044.1:c.2026A= XP_011515346.1:p.Asn676=
XM_011517045.1:c.1804A= XP_011515347.1:p.Asn602=
XM_017013460.1:c.1171A= XP_016868949.1:p.Asn391=
XM_017013462.2:c.1171A= XP_016868951.1:p.Asn391=
XM_024447163.1:c.1804A= XP_024302931.1:p.Asn602=
XM_024447164.1:c.1804A= XP_024302932.1:p.Asn602=
XM_024447165.1:c.1171A= XP_024302933.1:p.Asn391=
NM_002485.5:c.2050A= MANE Select NP_002476.2:p.Asn684=
NM_001024688.3:c.1804A= NP_001019859.1:p.Asn602=