Canonical Allele Identifier: CA181257948

Gene: NBN

Linked Data

• dbSNP Id: rs111239312
• MyVariant Identifiers: chr8:g.90965762C>A (hg19) ; chr8:g.89953534C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953534C>A , CM000670.2:g.89953534C>A	GRCh38
NC_000008.10:g.90965762C>A , CM000670.1:g.90965762C>A	GRCh37
NC_000008.9:g.91034938C>A	NCBI36
NG_008860.1:g.36138G>T , LRG_158:g.36138G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2857G>T
ENST00000517337.2:c.1309G>T	ENSP00000429971.2:p.Asp437Tyr
ENST00000523444.2:c.1309G>T	ENSP00000428252.2:p.Asp437Tyr
ENST00000697292.1:c.1555G>T	ENSP00000513229.1:p.Asp519Tyr
ENST00000697293.1:c.1555G>T	ENSP00000513230.1:p.Asp519Tyr
ENST00000697294.1:c.*1166G>T	ENSP00000513231.1:n.*1166G>T
ENST00000697295.1:c.*864G>T	ENSP00000513232.1:n.*864G>T
ENST00000697296.1:c.*1223G>T	ENSP00000513233.1:n.*1223G>T
ENST00000697297.1:n.3340G>T
ENST00000697298.1:c.1309G>T	ENSP00000513234.1:p.Asp437Tyr
ENST00000697299.1:c.1309G>T	ENSP00000513235.1:p.Asp437Tyr
ENST00000697300.1:c.*1159G>T	ENSP00000513236.1:n.*1159G>T
ENST00000697301.1:c.*1076G>T	ENSP00000513237.1:n.*1076G>T
ENST00000697302.1:c.*1076G>T	ENSP00000513238.1:n.*1076G>T
ENST00000697303.1:c.*1159G>T	ENSP00000513239.1:n.*1159G>T
ENST00000697304.1:c.1243G>T	ENSP00000513240.1:p.Asp415Tyr
ENST00000697306.1:c.*555G>T	ENSP00000513241.1:n.*555G>T
ENST00000697307.1:c.1555G>T	ENSP00000513242.1:p.Asp519Tyr
ENST00000697308.1:c.1555G>T	ENSP00000513243.1:p.Asp519Tyr
ENST00000697309.1:c.1555G>T	ENSP00000513244.1:p.Asp519Tyr
ENST00000697310.1:c.1555G>T	ENSP00000513245.1:p.Asp519Tyr
ENST00000697311.1:c.1555G>T	ENSP00000513246.1:p.Asp519Tyr
ENST00000697312.1:c.*953G>T	ENSP00000513247.1:n.*953G>T
ENST00000697313.1:n.2687+16830G>T
ENST00000697314.1:n.3346G>T
ENST00000697315.1:c.1555G>T	ENSP00000513248.1:p.Asp519Tyr
ENST00000697316.1:n.1676G>T
ENST00000697317.1:n.1665G>T
ENST00000697318.1:n.1667G>T
ENST00000265433.8:c.1555G>T MANE Select	ENSP00000265433.4:p.Asp519Tyr
ENST00000265433.7:c.1555G>T	ENSP00000265433.3:p.Asp519Tyr
ENST00000396252.6:c.*1428G>T	ENSP00000379551.2:n.*1428G>T
ENST00000409330.5:c.1309G>T	ENSP00000386924.1:p.Asp437Tyr
NM_001024688.2:c.1309G>T	NP_001019859.1:p.Asp437Tyr
NM_002485.4:c.1555G>T , LRG_158t1:c.1555G>T	NP_002476.2:p.Asp519Tyr
XM_011517044.1:c.1531G>T	XP_011515346.1:p.Asp511Tyr
XM_011517045.1:c.1309G>T	XP_011515347.1:p.Asp437Tyr
XR_928335.1:n.1694G>T
XM_017013460.1:c.676G>T	XP_016868949.1:p.Asp226Tyr
XM_017013462.2:c.676G>T	XP_016868951.1:p.Asp226Tyr
XM_024447163.1:c.1309G>T	XP_024302931.1:p.Asp437Tyr
XM_024447164.1:c.1309G>T	XP_024302932.1:p.Asp437Tyr
XM_024447165.1:c.676G>T	XP_024302933.1:p.Asp226Tyr
NM_002485.5:c.1555G>T MANE Select	NP_002476.2:p.Asp519Tyr
NM_001024688.3:c.1309G>T	NP_001019859.1:p.Asp437Tyr