Canonical Allele Identifier: CA371677319

Gene: NBN

Linked Data

• ClinVar Variation Id: 964295
• ClinVar RCV Id: RCV001238488 ; RCV003478747
• dbSNP Id: rs766602873
• gnomAD v4: 8-89947889-C-A
• MyVariant Identifiers: chr8:g.90960117C>A (hg19) ; chr8:g.89947889C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89947889C>A , CM000670.2:g.89947889C>A	GRCh38
NC_000008.10:g.90960117C>A , CM000670.1:g.90960117C>A	GRCh37
NC_000008.9:g.91029293C>A	NCBI36
NG_008860.1:g.41783G>T , LRG_158:g.41783G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3151G>T
ENST00000517337.2:c.1603G>T	ENSP00000429971.2:p.Glu535Ter
ENST00000523444.2:c.1603G>T	ENSP00000428252.2:p.Glu535Ter
ENST00000697292.1:c.1849G>T	ENSP00000513229.1:p.Glu617Ter
ENST00000697293.1:c.1849G>T	ENSP00000513230.1:p.Glu617Ter
ENST00000697294.1:c.*1460G>T	ENSP00000513231.1:n.*1460G>T
ENST00000697295.1:c.*1158G>T	ENSP00000513232.1:n.*1158G>T
ENST00000697296.1:c.*1517G>T	ENSP00000513233.1:n.*1517G>T
ENST00000697297.1:n.3634G>T
ENST00000697298.1:c.1603G>T	ENSP00000513234.1:p.Glu535Ter
ENST00000697299.1:c.1603G>T	ENSP00000513235.1:p.Glu535Ter
ENST00000697300.1:c.*1453G>T	ENSP00000513236.1:n.*1453G>T
ENST00000697301.1:c.*1370G>T	ENSP00000513237.1:n.*1370G>T
ENST00000697302.1:c.*1370G>T	ENSP00000513238.1:n.*1370G>T
ENST00000697303.1:c.*1453G>T	ENSP00000513239.1:n.*1453G>T
ENST00000697304.1:c.1537G>T	ENSP00000513240.1:p.Glu513Ter
ENST00000697306.1:c.*872G>T	ENSP00000513241.1:n.*872G>T
ENST00000697307.1:c.1846-4523G>T	ENSP00000513242.1:n.1846-4523G>T
ENST00000697308.1:c.1846-1594G>T	ENSP00000513243.1:n.1846-1594G>T
ENST00000697309.1:c.1849G>T	ENSP00000513244.1:p.Glu617Ter
ENST00000697310.1:c.1849G>T	ENSP00000513245.1:p.Glu617Ter
ENST00000697311.1:c.1849G>T	ENSP00000513246.1:p.Glu617Ter
ENST00000697312.1:c.*1247G>T	ENSP00000513247.1:n.*1247G>T
ENST00000697313.1:n.2688-12277G>T
ENST00000697314.1:n.3636+5355G>T
ENST00000697315.1:c.1849G>T	ENSP00000513248.1:p.Glu617Ter
ENST00000697316.1:n.1970G>T
ENST00000697317.1:n.1959G>T
ENST00000265433.8:c.1849G>T MANE Select	ENSP00000265433.4:p.Glu617Ter
ENST00000265433.7:c.1849G>T	ENSP00000265433.3:p.Glu617Ter
ENST00000396252.6:c.*1722G>T	ENSP00000379551.2:n.*1722G>T
ENST00000409330.5:c.1603G>T	ENSP00000386924.1:p.Glu535Ter
ENST00000613033.1:c.115G>T	ENSP00000484487.1:p.Glu39Ter
NM_001024688.2:c.1603G>T	NP_001019859.1:p.Glu535Ter
NM_002485.4:c.1849G>T , LRG_158t1:c.1849G>T	NP_002476.2:p.Glu617Ter
XM_011517044.1:c.1825G>T	XP_011515346.1:p.Glu609Ter
XM_011517045.1:c.1603G>T	XP_011515347.1:p.Glu535Ter
XR_928335.1:n.1988G>T
XM_017013460.1:c.970G>T	XP_016868949.1:p.Glu324Ter
XM_017013462.2:c.970G>T	XP_016868951.1:p.Glu324Ter
XM_024447163.1:c.1603G>T	XP_024302931.1:p.Glu535Ter
XM_024447164.1:c.1603G>T	XP_024302932.1:p.Glu535Ter
XM_024447165.1:c.970G>T	XP_024302933.1:p.Glu324Ter
NM_002485.5:c.1849G>T MANE Select	NP_002476.2:p.Glu617Ter
NM_001024688.3:c.1603G>T	NP_001019859.1:p.Glu535Ter