Canonical Allele Identifier: CA371655767
Community Standard Title: NM_002485.5(NBN):c.1480C>T (p.Gln494Ter)
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89953609G>A , CM000670.2:g.89953609G>A GRCh38
NC_000008.10:g.90965837G>A , CM000670.1:g.90965837G>A GRCh37
NC_000008.9:g.91035013G>A NCBI36
NG_008860.1:g.36063C>T , LRG_158:g.36063C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002485.5:c.1480C>T MANE Select NP_002476.2:p.Gln494Ter
ENST00000265433.8:c.1480C>T MANE Select ENSP00000265433.4:p.Gln494Ter
NM_001024688.2:c.1234C>T NP_001019859.1:p.Gln412Ter
NM_001024688.3:c.1234C>T NP_001019859.1:p.Gln412Ter
NM_002485.4:c.1480C>T , LRG_158t1:c.1480C>T NP_002476.2:p.Gln494Ter
ENST00000265433.7:c.1480C>T ENSP00000265433.3:p.Gln494Ter
ENST00000396252.6:c.*1353C>T ENSP00000379551.2:n.*1353C>T
ENST00000409330.5:c.1234C>T ENSP00000386924.1:p.Gln412Ter
ENST00000494804.2:n.2782C>T
ENST00000517337.2:c.1234C>T ENSP00000429971.2:p.Gln412Ter
ENST00000523444.2:c.1234C>T ENSP00000428252.2:p.Gln412Ter
ENST00000697292.1:c.1480C>T ENSP00000513229.1:p.Gln494Ter
ENST00000697293.1:c.1480C>T ENSP00000513230.1:p.Gln494Ter
ENST00000697294.1:c.*1091C>T ENSP00000513231.1:n.*1091C>T
ENST00000697295.1:c.*789C>T ENSP00000513232.1:n.*789C>T
ENST00000697296.1:c.*1148C>T ENSP00000513233.1:n.*1148C>T
ENST00000697297.1:n.3265C>T
ENST00000697298.1:c.1234C>T ENSP00000513234.1:p.Gln412Ter
ENST00000697299.1:c.1234C>T ENSP00000513235.1:p.Gln412Ter
ENST00000697300.1:c.*1084C>T ENSP00000513236.1:n.*1084C>T
ENST00000697301.1:c.*1001C>T ENSP00000513237.1:n.*1001C>T
ENST00000697302.1:c.*1001C>T ENSP00000513238.1:n.*1001C>T
ENST00000697303.1:c.*1084C>T ENSP00000513239.1:n.*1084C>T
ENST00000697304.1:c.1168C>T ENSP00000513240.1:p.Gln390Ter
ENST00000697306.1:c.*480C>T ENSP00000513241.1:n.*480C>T
ENST00000697307.1:c.1480C>T ENSP00000513242.1:p.Gln494Ter
ENST00000697308.1:c.1480C>T ENSP00000513243.1:p.Gln494Ter
ENST00000697309.1:c.1480C>T ENSP00000513244.1:p.Gln494Ter
ENST00000697310.1:c.1480C>T ENSP00000513245.1:p.Gln494Ter
ENST00000697311.1:c.1480C>T ENSP00000513246.1:p.Gln494Ter
ENST00000697312.1:c.*878C>T ENSP00000513247.1:n.*878C>T
ENST00000697313.1:n.2687+16755C>T
ENST00000697314.1:n.3271C>T
ENST00000697315.1:c.1480C>T ENSP00000513248.1:p.Gln494Ter
ENST00000697316.1:n.1601C>T
ENST00000697317.1:n.1590C>T
ENST00000697318.1:n.1592C>T
XM_011517044.1:c.1456C>T XP_011515346.1:p.Gln486Ter
XM_011517045.1:c.1234C>T XP_011515347.1:p.Gln412Ter
XM_017013460.1:c.601C>T XP_016868949.1:p.Gln201Ter
XM_017013462.2:c.601C>T XP_016868951.1:p.Gln201Ter
XM_024447163.1:c.1234C>T XP_024302931.1:p.Gln412Ter
XM_024447164.1:c.1234C>T XP_024302932.1:p.Gln412Ter
XM_024447165.1:c.601C>T XP_024302933.1:p.Gln201Ter
XR_928335.1:n.1619C>T