Canonical Allele Identifier: CA371655576

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90965749A>T (hg19) ; chr8:g.89953521A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953521A>T , CM000670.2:g.89953521A>T	GRCh38
NC_000008.10:g.90965749A>T , CM000670.1:g.90965749A>T	GRCh37
NC_000008.9:g.91034925A>T	NCBI36
NG_008860.1:g.36151T>A , LRG_158:g.36151T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2870T>A
ENST00000517337.2:c.1322T>A	ENSP00000429971.2:p.Phe441Tyr
ENST00000523444.2:c.1322T>A	ENSP00000428252.2:p.Phe441Tyr
ENST00000697292.1:c.1568T>A	ENSP00000513229.1:p.Phe523Tyr
ENST00000697293.1:c.1568T>A	ENSP00000513230.1:p.Phe523Tyr
ENST00000697294.1:c.*1179T>A	ENSP00000513231.1:n.*1179T>A
ENST00000697295.1:c.*877T>A	ENSP00000513232.1:n.*877T>A
ENST00000697296.1:c.*1236T>A	ENSP00000513233.1:n.*1236T>A
ENST00000697297.1:n.3353T>A
ENST00000697298.1:c.1322T>A	ENSP00000513234.1:p.Phe441Tyr
ENST00000697299.1:c.1322T>A	ENSP00000513235.1:p.Phe441Tyr
ENST00000697300.1:c.*1172T>A	ENSP00000513236.1:n.*1172T>A
ENST00000697301.1:c.*1089T>A	ENSP00000513237.1:n.*1089T>A
ENST00000697302.1:c.*1089T>A	ENSP00000513238.1:n.*1089T>A
ENST00000697303.1:c.*1172T>A	ENSP00000513239.1:n.*1172T>A
ENST00000697304.1:c.1256T>A	ENSP00000513240.1:p.Phe419Tyr
ENST00000697306.1:c.*568T>A	ENSP00000513241.1:n.*568T>A
ENST00000697307.1:c.1568T>A	ENSP00000513242.1:p.Phe523Tyr
ENST00000697308.1:c.1568T>A	ENSP00000513243.1:p.Phe523Tyr
ENST00000697309.1:c.1568T>A	ENSP00000513244.1:p.Phe523Tyr
ENST00000697310.1:c.1568T>A	ENSP00000513245.1:p.Phe523Tyr
ENST00000697311.1:c.1568T>A	ENSP00000513246.1:p.Phe523Tyr
ENST00000697312.1:c.*966T>A	ENSP00000513247.1:n.*966T>A
ENST00000697313.1:n.2687+16843T>A
ENST00000697314.1:n.3359T>A
ENST00000697315.1:c.1568T>A	ENSP00000513248.1:p.Phe523Tyr
ENST00000697316.1:n.1689T>A
ENST00000697317.1:n.1678T>A
ENST00000697318.1:n.1680T>A
ENST00000265433.8:c.1568T>A MANE Select	ENSP00000265433.4:p.Phe523Tyr
ENST00000265433.7:c.1568T>A	ENSP00000265433.3:p.Phe523Tyr
ENST00000396252.6:c.*1441T>A	ENSP00000379551.2:n.*1441T>A
ENST00000409330.5:c.1322T>A	ENSP00000386924.1:p.Phe441Tyr
NM_001024688.2:c.1322T>A	NP_001019859.1:p.Phe441Tyr
NM_002485.4:c.1568T>A , LRG_158t1:c.1568T>A	NP_002476.2:p.Phe523Tyr
XM_011517044.1:c.1544T>A	XP_011515346.1:p.Phe515Tyr
XM_011517045.1:c.1322T>A	XP_011515347.1:p.Phe441Tyr
XR_928335.1:n.1707T>A
XM_017013460.1:c.689T>A	XP_016868949.1:p.Phe230Tyr
XM_017013462.2:c.689T>A	XP_016868951.1:p.Phe230Tyr
XM_024447163.1:c.1322T>A	XP_024302931.1:p.Phe441Tyr
XM_024447164.1:c.1322T>A	XP_024302932.1:p.Phe441Tyr
XM_024447165.1:c.689T>A	XP_024302933.1:p.Phe230Tyr
NM_002485.5:c.1568T>A MANE Select	NP_002476.2:p.Phe523Tyr
NM_001024688.3:c.1322T>A	NP_001019859.1:p.Phe441Tyr