Canonical Allele Identifier: CA1801422918
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953524A= , CM000670.2:g.89953524A= GRCh38
NC_000008.10:g.90965752A= , CM000670.1:g.90965752A= GRCh37
NC_000008.9:g.91034928A= NCBI36
NG_008860.1:g.36148T= , LRG_158:g.36148T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2867T=
ENST00000517337.2:c.1319T= ENSP00000429971.2:p.Leu440=
ENST00000523444.2:c.1319T= ENSP00000428252.2:p.Leu440=
ENST00000697292.1:c.1565T= ENSP00000513229.1:p.Leu522=
ENST00000697293.1:c.1565T= ENSP00000513230.1:p.Leu522=
ENST00000697294.1:c.*1176T= ENSP00000513231.1:n.*1176T=
ENST00000697295.1:c.*874T= ENSP00000513232.1:n.*874T=
ENST00000697296.1:c.*1233T= ENSP00000513233.1:n.*1233T=
ENST00000697297.1:n.3350T=
ENST00000697298.1:c.1319T= ENSP00000513234.1:p.Leu440=
ENST00000697299.1:c.1319T= ENSP00000513235.1:p.Leu440=
ENST00000697300.1:c.*1169T= ENSP00000513236.1:n.*1169T=
ENST00000697301.1:c.*1086T= ENSP00000513237.1:n.*1086T=
ENST00000697302.1:c.*1086T= ENSP00000513238.1:n.*1086T=
ENST00000697303.1:c.*1169T= ENSP00000513239.1:n.*1169T=
ENST00000697304.1:c.1253T= ENSP00000513240.1:p.Leu418=
ENST00000697306.1:c.*565T= ENSP00000513241.1:n.*565T=
ENST00000697307.1:c.1565T= ENSP00000513242.1:p.Leu522=
ENST00000697308.1:c.1565T= ENSP00000513243.1:p.Leu522=
ENST00000697309.1:c.1565T= ENSP00000513244.1:p.Leu522=
ENST00000697310.1:c.1565T= ENSP00000513245.1:p.Leu522=
ENST00000697311.1:c.1565T= ENSP00000513246.1:p.Leu522=
ENST00000697312.1:c.*963T= ENSP00000513247.1:n.*963T=
ENST00000697313.1:n.2687+16840T=
ENST00000697314.1:n.3356T=
ENST00000697315.1:c.1565T= ENSP00000513248.1:p.Leu522=
ENST00000697316.1:n.1686T=
ENST00000697317.1:n.1675T=
ENST00000697318.1:n.1677T=
ENST00000265433.8:c.1565T= MANE Select ENSP00000265433.4:p.Leu522=
ENST00000265433.7:c.1565T= ENSP00000265433.3:p.Leu522=
ENST00000396252.6:c.*1438T= ENSP00000379551.2:n.*1438T=
ENST00000409330.5:c.1319T= ENSP00000386924.1:p.Leu440=
NM_001024688.2:c.1319T= NP_001019859.1:p.Leu440=
NM_002485.4:c.1565T= , LRG_158t1:c.1565T= NP_002476.2:p.Leu522=
XM_011517044.1:c.1541T= XP_011515346.1:p.Leu514=
XM_011517045.1:c.1319T= XP_011515347.1:p.Leu440=
XR_928335.1:n.1704T=
XM_017013460.1:c.686T= XP_016868949.1:p.Leu229=
XM_017013462.2:c.686T= XP_016868951.1:p.Leu229=
XM_024447163.1:c.1319T= XP_024302931.1:p.Leu440=
XM_024447164.1:c.1319T= XP_024302932.1:p.Leu440=
XM_024447165.1:c.686T= XP_024302933.1:p.Leu229=
NM_002485.5:c.1565T= MANE Select NP_002476.2:p.Leu522=
NM_001024688.3:c.1319T= NP_001019859.1:p.Leu440=