Canonical Allele Identifier: CA371656070
Community Standard Title: NM_002485.5(NBN):c.1342C>T (p.Gln448Ter)
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89955338G>A , CM000670.2:g.89955338G>A GRCh38
NC_000008.10:g.90967566G>A , CM000670.1:g.90967566G>A GRCh37
NC_000008.9:g.91036742G>A NCBI36
NG_008860.1:g.34334C>T , LRG_158:g.34334C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002485.5:c.1342C>T MANE Select NP_002476.2:p.Gln448Ter
ENST00000265433.8:c.1342C>T MANE Select ENSP00000265433.4:p.Gln448Ter
NM_001024688.2:c.1096C>T NP_001019859.1:p.Gln366Ter
NM_001024688.3:c.1096C>T NP_001019859.1:p.Gln366Ter
NM_002485.4:c.1342C>T , LRG_158t1:c.1342C>T NP_002476.2:p.Gln448Ter
ENST00000265433.7:c.1342C>T ENSP00000265433.3:p.Gln448Ter
ENST00000396252.6:c.*1215C>T ENSP00000379551.2:n.*1215C>T
ENST00000409330.5:c.1096C>T ENSP00000386924.1:p.Gln366Ter
ENST00000494804.2:n.2644C>T
ENST00000517337.2:c.1096C>T ENSP00000429971.2:p.Gln366Ter
ENST00000523444.2:c.1096C>T ENSP00000428252.2:p.Gln366Ter
ENST00000697292.1:c.1342C>T ENSP00000513229.1:p.Gln448Ter
ENST00000697293.1:c.1342C>T ENSP00000513230.1:p.Gln448Ter
ENST00000697294.1:c.*953C>T ENSP00000513231.1:n.*953C>T
ENST00000697295.1:c.*651C>T ENSP00000513232.1:n.*651C>T
ENST00000697296.1:c.*1010C>T ENSP00000513233.1:n.*1010C>T
ENST00000697297.1:n.3127C>T
ENST00000697298.1:c.1096C>T ENSP00000513234.1:p.Gln366Ter
ENST00000697299.1:c.1096C>T ENSP00000513235.1:p.Gln366Ter
ENST00000697300.1:c.*946C>T ENSP00000513236.1:n.*946C>T
ENST00000697301.1:c.*863C>T ENSP00000513237.1:n.*863C>T
ENST00000697302.1:c.*863C>T ENSP00000513238.1:n.*863C>T
ENST00000697303.1:c.*946C>T ENSP00000513239.1:n.*946C>T
ENST00000697304.1:c.1030C>T ENSP00000513240.1:p.Gln344Ter
ENST00000697306.1:c.*342C>T ENSP00000513241.1:n.*342C>T
ENST00000697307.1:c.1342C>T ENSP00000513242.1:p.Gln448Ter
ENST00000697308.1:c.1342C>T ENSP00000513243.1:p.Gln448Ter
ENST00000697309.1:c.1342C>T ENSP00000513244.1:p.Gln448Ter
ENST00000697310.1:c.1342C>T ENSP00000513245.1:p.Gln448Ter
ENST00000697311.1:c.1342C>T ENSP00000513246.1:p.Gln448Ter
ENST00000697312.1:c.*740C>T ENSP00000513247.1:n.*740C>T
ENST00000697313.1:n.2687+15026C>T
ENST00000697314.1:n.3133C>T
ENST00000697315.1:c.1342C>T ENSP00000513248.1:p.Gln448Ter
ENST00000697316.1:n.1463C>T
ENST00000697317.1:n.1452C>T
ENST00000697318.1:n.1454C>T
XM_011517044.1:c.1318C>T XP_011515346.1:p.Gln440Ter
XM_011517045.1:c.1096C>T XP_011515347.1:p.Gln366Ter
XM_011517046.1:c.1342C>T XP_011515348.1:p.Gln448Ter
XM_017013460.1:c.463C>T XP_016868949.1:p.Gln155Ter
XM_017013462.2:c.463C>T XP_016868951.1:p.Gln155Ter
XM_024447163.1:c.1096C>T XP_024302931.1:p.Gln366Ter
XM_024447164.1:c.1096C>T XP_024302932.1:p.Gln366Ter
XM_024447165.1:c.463C>T XP_024302933.1:p.Gln155Ter
XR_928335.1:n.1479C>T