Canonical Allele Identifier: CA1801422900
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953494A= , CM000670.2:g.89953494A= GRCh38
NC_000008.10:g.90965722A= , CM000670.1:g.90965722A= GRCh37
NC_000008.9:g.91034898A= NCBI36
NG_008860.1:g.36178T= , LRG_158:g.36178T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2897T=
ENST00000517337.2:c.1349T= ENSP00000429971.2:p.Val450=
ENST00000523444.2:c.1349T= ENSP00000428252.2:p.Val450=
ENST00000697292.1:c.1595T= ENSP00000513229.1:p.Val532=
ENST00000697293.1:c.1595T= ENSP00000513230.1:p.Val532=
ENST00000697294.1:c.*1206T= ENSP00000513231.1:n.*1206T=
ENST00000697295.1:c.*904T= ENSP00000513232.1:n.*904T=
ENST00000697296.1:c.*1263T= ENSP00000513233.1:n.*1263T=
ENST00000697297.1:n.3380T=
ENST00000697298.1:c.1349T= ENSP00000513234.1:p.Val450=
ENST00000697299.1:c.1349T= ENSP00000513235.1:p.Val450=
ENST00000697300.1:c.*1199T= ENSP00000513236.1:n.*1199T=
ENST00000697301.1:c.*1116T= ENSP00000513237.1:n.*1116T=
ENST00000697302.1:c.*1116T= ENSP00000513238.1:n.*1116T=
ENST00000697303.1:c.*1199T= ENSP00000513239.1:n.*1199T=
ENST00000697304.1:c.1283T= ENSP00000513240.1:p.Val428=
ENST00000697306.1:c.*595T= ENSP00000513241.1:n.*595T=
ENST00000697307.1:c.1595T= ENSP00000513242.1:p.Val532=
ENST00000697308.1:c.1595T= ENSP00000513243.1:p.Val532=
ENST00000697309.1:c.1595T= ENSP00000513244.1:p.Val532=
ENST00000697310.1:c.1595T= ENSP00000513245.1:p.Val532=
ENST00000697311.1:c.1595T= ENSP00000513246.1:p.Val532=
ENST00000697312.1:c.*993T= ENSP00000513247.1:n.*993T=
ENST00000697313.1:n.2687+16870T=
ENST00000697314.1:n.3386T=
ENST00000697315.1:c.1595T= ENSP00000513248.1:p.Val532=
ENST00000697316.1:n.1716T=
ENST00000697317.1:n.1705T=
ENST00000697318.1:n.1707T=
ENST00000265433.8:c.1595T= MANE Select ENSP00000265433.4:p.Val532=
ENST00000265433.7:c.1595T= ENSP00000265433.3:p.Val532=
ENST00000396252.6:c.*1468T= ENSP00000379551.2:n.*1468T=
ENST00000409330.5:c.1349T= ENSP00000386924.1:p.Val450=
NM_001024688.2:c.1349T= NP_001019859.1:p.Val450=
NM_002485.4:c.1595T= , LRG_158t1:c.1595T= NP_002476.2:p.Val532=
XM_011517044.1:c.1571T= XP_011515346.1:p.Val524=
XM_011517045.1:c.1349T= XP_011515347.1:p.Val450=
XR_928335.1:n.1734T=
XM_017013460.1:c.716T= XP_016868949.1:p.Val239=
XM_017013462.2:c.716T= XP_016868951.1:p.Val239=
XM_024447163.1:c.1349T= XP_024302931.1:p.Val450=
XM_024447164.1:c.1349T= XP_024302932.1:p.Val450=
XM_024447165.1:c.716T= XP_024302933.1:p.Val239=
NM_002485.5:c.1595T= MANE Select NP_002476.2:p.Val532=
NM_001024688.3:c.1349T= NP_001019859.1:p.Val450=