Canonical Allele Identifier: CA181257881
Community Standard Title: NM_002485.5(NBN):c.1622C>T (p.Ala541Val)
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953467G>A , CM000670.2:g.89953467G>A GRCh38
NC_000008.10:g.90965695G>A , CM000670.1:g.90965695G>A GRCh37
NC_000008.9:g.91034871G>A NCBI36
NG_008860.1:g.36205C>T , LRG_158:g.36205C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002485.5:c.1622C>T MANE Select NP_002476.2:p.Ala541Val
ENST00000265433.8:c.1622C>T MANE Select ENSP00000265433.4:p.Ala541Val
NM_001024688.2:c.1376C>T NP_001019859.1:p.Ala459Val
NM_001024688.3:c.1376C>T NP_001019859.1:p.Ala459Val
NM_002485.4:c.1622C>T , LRG_158t1:c.1622C>T NP_002476.2:p.Ala541Val
ENST00000265433.7:c.1622C>T ENSP00000265433.3:p.Ala541Val
ENST00000396252.6:c.*1495C>T ENSP00000379551.2:n.*1495C>T
ENST00000409330.5:c.1376C>T ENSP00000386924.1:p.Ala459Val
ENST00000494804.2:n.2924C>T
ENST00000517337.2:c.1376C>T ENSP00000429971.2:p.Ala459Val
ENST00000523444.2:c.1376C>T ENSP00000428252.2:p.Ala459Val
ENST00000697292.1:c.1622C>T ENSP00000513229.1:p.Ala541Val
ENST00000697293.1:c.1622C>T ENSP00000513230.1:p.Ala541Val
ENST00000697294.1:c.*1233C>T ENSP00000513231.1:n.*1233C>T
ENST00000697295.1:c.*931C>T ENSP00000513232.1:n.*931C>T
ENST00000697296.1:c.*1290C>T ENSP00000513233.1:n.*1290C>T
ENST00000697297.1:n.3407C>T
ENST00000697298.1:c.1376C>T ENSP00000513234.1:p.Ala459Val
ENST00000697299.1:c.1376C>T ENSP00000513235.1:p.Ala459Val
ENST00000697300.1:c.*1226C>T ENSP00000513236.1:n.*1226C>T
ENST00000697301.1:c.*1143C>T ENSP00000513237.1:n.*1143C>T
ENST00000697302.1:c.*1143C>T ENSP00000513238.1:n.*1143C>T
ENST00000697303.1:c.*1226C>T ENSP00000513239.1:n.*1226C>T
ENST00000697304.1:c.1310C>T ENSP00000513240.1:p.Ala437Val
ENST00000697306.1:c.*622C>T ENSP00000513241.1:n.*622C>T
ENST00000697307.1:c.1622C>T ENSP00000513242.1:p.Ala541Val
ENST00000697308.1:c.1622C>T ENSP00000513243.1:p.Ala541Val
ENST00000697309.1:c.1622C>T ENSP00000513244.1:p.Ala541Val
ENST00000697310.1:c.1622C>T ENSP00000513245.1:p.Ala541Val
ENST00000697311.1:c.1622C>T ENSP00000513246.1:p.Ala541Val
ENST00000697312.1:c.*1020C>T ENSP00000513247.1:n.*1020C>T
ENST00000697313.1:n.2687+16897C>T
ENST00000697314.1:n.3413C>T
ENST00000697315.1:c.1622C>T ENSP00000513248.1:p.Ala541Val
ENST00000697316.1:n.1743C>T
ENST00000697317.1:n.1732C>T
ENST00000697318.1:n.1734C>T
XM_011517044.1:c.1598C>T XP_011515346.1:p.Ala533Val
XM_011517045.1:c.1376C>T XP_011515347.1:p.Ala459Val
XM_017013460.1:c.743C>T XP_016868949.1:p.Ala248Val
XM_017013462.2:c.743C>T XP_016868951.1:p.Ala248Val
XM_024447163.1:c.1376C>T XP_024302931.1:p.Ala459Val
XM_024447164.1:c.1376C>T XP_024302932.1:p.Ala459Val
XM_024447165.1:c.743C>T XP_024302933.1:p.Ala248Val
XR_928335.1:n.1761C>T