Canonical Allele Identifier: CA371677296

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90960108T>A (hg19) ; chr8:g.89947880T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89947880T>A , CM000670.2:g.89947880T>A	GRCh38
NC_000008.10:g.90960108T>A , CM000670.1:g.90960108T>A	GRCh37
NC_000008.9:g.91029284T>A	NCBI36
NG_008860.1:g.41792A>T , LRG_158:g.41792A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.3160A>T
ENST00000517337.2:c.1612A>T	ENSP00000429971.2:p.Ile538Phe
ENST00000523444.2:c.1612A>T	ENSP00000428252.2:p.Ile538Phe
ENST00000697292.1:c.1858A>T	ENSP00000513229.1:p.Ile620Phe
ENST00000697293.1:c.1858A>T	ENSP00000513230.1:p.Ile620Phe
ENST00000697294.1:c.*1469A>T	ENSP00000513231.1:n.*1469A>T
ENST00000697295.1:c.*1167A>T	ENSP00000513232.1:n.*1167A>T
ENST00000697296.1:c.*1526A>T	ENSP00000513233.1:n.*1526A>T
ENST00000697297.1:n.3643A>T
ENST00000697298.1:c.1612A>T	ENSP00000513234.1:p.Ile538Phe
ENST00000697299.1:c.1612A>T	ENSP00000513235.1:p.Ile538Phe
ENST00000697300.1:c.*1462A>T	ENSP00000513236.1:n.*1462A>T
ENST00000697301.1:c.*1379A>T	ENSP00000513237.1:n.*1379A>T
ENST00000697302.1:c.*1379A>T	ENSP00000513238.1:n.*1379A>T
ENST00000697303.1:c.*1462A>T	ENSP00000513239.1:n.*1462A>T
ENST00000697304.1:c.1546A>T	ENSP00000513240.1:p.Ile516Phe
ENST00000697306.1:c.*881A>T	ENSP00000513241.1:n.*881A>T
ENST00000697307.1:c.1846-4514A>T	ENSP00000513242.1:n.1846-4514A>T
ENST00000697308.1:c.1846-1585A>T	ENSP00000513243.1:n.1846-1585A>T
ENST00000697309.1:c.1858A>T	ENSP00000513244.1:p.Ile620Phe
ENST00000697310.1:c.1858A>T	ENSP00000513245.1:p.Ile620Phe
ENST00000697311.1:c.1858A>T	ENSP00000513246.1:p.Ile620Phe
ENST00000697312.1:c.*1256A>T	ENSP00000513247.1:n.*1256A>T
ENST00000697313.1:n.2688-12268A>T
ENST00000697314.1:n.3636+5364A>T
ENST00000697315.1:c.1858A>T	ENSP00000513248.1:p.Ile620Phe
ENST00000697316.1:n.1979A>T
ENST00000697317.1:n.1968A>T
ENST00000265433.8:c.1858A>T MANE Select	ENSP00000265433.4:p.Ile620Phe
ENST00000265433.7:c.1858A>T	ENSP00000265433.3:p.Ile620Phe
ENST00000396252.6:c.*1731A>T	ENSP00000379551.2:n.*1731A>T
ENST00000409330.5:c.1612A>T	ENSP00000386924.1:p.Ile538Phe
ENST00000613033.1:c.124A>T	ENSP00000484487.1:p.Ile42Phe
NM_001024688.2:c.1612A>T	NP_001019859.1:p.Ile538Phe
NM_002485.4:c.1858A>T , LRG_158t1:c.1858A>T	NP_002476.2:p.Ile620Phe
XM_011517044.1:c.1834A>T	XP_011515346.1:p.Ile612Phe
XM_011517045.1:c.1612A>T	XP_011515347.1:p.Ile538Phe
XR_928335.1:n.1997A>T
XM_017013460.1:c.979A>T	XP_016868949.1:p.Ile327Phe
XM_017013462.2:c.979A>T	XP_016868951.1:p.Ile327Phe
XM_024447163.1:c.1612A>T	XP_024302931.1:p.Ile538Phe
XM_024447164.1:c.1612A>T	XP_024302932.1:p.Ile538Phe
XM_024447165.1:c.979A>T	XP_024302933.1:p.Ile327Phe
NM_002485.5:c.1858A>T MANE Select	NP_002476.2:p.Ile620Phe
NM_001024688.3:c.1612A>T	NP_001019859.1:p.Ile538Phe