Canonical Allele Identifier: CA371655460

Gene: NBN

Linked Data

• ClinVar Variation Id: 2123305
• ClinVar RCV Id: RCV003035347
• MyVariant Identifiers: chr8:g.90965696C>T (hg19) ; chr8:g.89953468C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953468C>T , CM000670.2:g.89953468C>T	GRCh38
NC_000008.10:g.90965696C>T , CM000670.1:g.90965696C>T	GRCh37
NC_000008.9:g.91034872C>T	NCBI36
NG_008860.1:g.36204G>A , LRG_158:g.36204G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2923G>A
ENST00000517337.2:c.1375G>A	ENSP00000429971.2:p.Ala459Thr
ENST00000523444.2:c.1375G>A	ENSP00000428252.2:p.Ala459Thr
ENST00000697292.1:c.1621G>A	ENSP00000513229.1:p.Ala541Thr
ENST00000697293.1:c.1621G>A	ENSP00000513230.1:p.Ala541Thr
ENST00000697294.1:c.*1232G>A	ENSP00000513231.1:n.*1232G>A
ENST00000697295.1:c.*930G>A	ENSP00000513232.1:n.*930G>A
ENST00000697296.1:c.*1289G>A	ENSP00000513233.1:n.*1289G>A
ENST00000697297.1:n.3406G>A
ENST00000697298.1:c.1375G>A	ENSP00000513234.1:p.Ala459Thr
ENST00000697299.1:c.1375G>A	ENSP00000513235.1:p.Ala459Thr
ENST00000697300.1:c.*1225G>A	ENSP00000513236.1:n.*1225G>A
ENST00000697301.1:c.*1142G>A	ENSP00000513237.1:n.*1142G>A
ENST00000697302.1:c.*1142G>A	ENSP00000513238.1:n.*1142G>A
ENST00000697303.1:c.*1225G>A	ENSP00000513239.1:n.*1225G>A
ENST00000697304.1:c.1309G>A	ENSP00000513240.1:p.Ala437Thr
ENST00000697306.1:c.*621G>A	ENSP00000513241.1:n.*621G>A
ENST00000697307.1:c.1621G>A	ENSP00000513242.1:p.Ala541Thr
ENST00000697308.1:c.1621G>A	ENSP00000513243.1:p.Ala541Thr
ENST00000697309.1:c.1621G>A	ENSP00000513244.1:p.Ala541Thr
ENST00000697310.1:c.1621G>A	ENSP00000513245.1:p.Ala541Thr
ENST00000697311.1:c.1621G>A	ENSP00000513246.1:p.Ala541Thr
ENST00000697312.1:c.*1019G>A	ENSP00000513247.1:n.*1019G>A
ENST00000697313.1:n.2687+16896G>A
ENST00000697314.1:n.3412G>A
ENST00000697315.1:c.1621G>A	ENSP00000513248.1:p.Ala541Thr
ENST00000697316.1:n.1742G>A
ENST00000697317.1:n.1731G>A
ENST00000697318.1:n.1733G>A
ENST00000265433.8:c.1621G>A MANE Select	ENSP00000265433.4:p.Ala541Thr
ENST00000265433.7:c.1621G>A	ENSP00000265433.3:p.Ala541Thr
ENST00000396252.6:c.*1494G>A	ENSP00000379551.2:n.*1494G>A
ENST00000409330.5:c.1375G>A	ENSP00000386924.1:p.Ala459Thr
NM_001024688.2:c.1375G>A	NP_001019859.1:p.Ala459Thr
NM_002485.4:c.1621G>A , LRG_158t1:c.1621G>A	NP_002476.2:p.Ala541Thr
XM_011517044.1:c.1597G>A	XP_011515346.1:p.Ala533Thr
XM_011517045.1:c.1375G>A	XP_011515347.1:p.Ala459Thr
XR_928335.1:n.1760G>A
XM_017013460.1:c.742G>A	XP_016868949.1:p.Ala248Thr
XM_017013462.2:c.742G>A	XP_016868951.1:p.Ala248Thr
XM_024447163.1:c.1375G>A	XP_024302931.1:p.Ala459Thr
XM_024447164.1:c.1375G>A	XP_024302932.1:p.Ala459Thr
XM_024447165.1:c.742G>A	XP_024302933.1:p.Ala248Thr
NM_002485.5:c.1621G>A MANE Select	NP_002476.2:p.Ala541Thr
NM_001024688.3:c.1375G>A	NP_001019859.1:p.Ala459Thr