Canonical Allele Identifier: CA371655227

Gene: NBN

Linked Data

• ClinVar Variation Id: 1493686
• ClinVar RCV Id: RCV001986667
• dbSNP Id: rs1255733657
• MyVariant Identifiers: chr8:g.90965590A>C (hg19) ; chr8:g.89953362A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953362A>C , CM000670.2:g.89953362A>C	GRCh38
NC_000008.10:g.90965590A>C , CM000670.1:g.90965590A>C	GRCh37
NC_000008.9:g.91034766A>C	NCBI36
NG_008860.1:g.36310T>G , LRG_158:g.36310T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3029T>G
ENST00000517337.2:c.1481T>G	ENSP00000429971.2:p.Ile494Ser
ENST00000523444.2:c.1481T>G	ENSP00000428252.2:p.Ile494Ser
ENST00000697292.1:c.1727T>G	ENSP00000513229.1:p.Ile576Ser
ENST00000697293.1:c.1727T>G	ENSP00000513230.1:p.Ile576Ser
ENST00000697294.1:c.*1338T>G	ENSP00000513231.1:n.*1338T>G
ENST00000697295.1:c.*1036T>G	ENSP00000513232.1:n.*1036T>G
ENST00000697296.1:c.*1395T>G	ENSP00000513233.1:n.*1395T>G
ENST00000697297.1:n.3512T>G
ENST00000697298.1:c.1481T>G	ENSP00000513234.1:p.Ile494Ser
ENST00000697299.1:c.1481T>G	ENSP00000513235.1:p.Ile494Ser
ENST00000697300.1:c.*1331T>G	ENSP00000513236.1:n.*1331T>G
ENST00000697301.1:c.*1248T>G	ENSP00000513237.1:n.*1248T>G
ENST00000697302.1:c.*1248T>G	ENSP00000513238.1:n.*1248T>G
ENST00000697303.1:c.*1331T>G	ENSP00000513239.1:n.*1331T>G
ENST00000697304.1:c.1415T>G	ENSP00000513240.1:p.Ile472Ser
ENST00000697306.1:c.*727T>G	ENSP00000513241.1:n.*727T>G
ENST00000697307.1:c.1727T>G	ENSP00000513242.1:p.Ile576Ser
ENST00000697308.1:c.1727T>G	ENSP00000513243.1:p.Ile576Ser
ENST00000697309.1:c.1727T>G	ENSP00000513244.1:p.Ile576Ser
ENST00000697310.1:c.1727T>G	ENSP00000513245.1:p.Ile576Ser
ENST00000697311.1:c.1727T>G	ENSP00000513246.1:p.Ile576Ser
ENST00000697312.1:c.*1125T>G	ENSP00000513247.1:n.*1125T>G
ENST00000697313.1:n.2687+17002T>G
ENST00000697314.1:n.3518T>G
ENST00000697315.1:c.1727T>G	ENSP00000513248.1:p.Ile576Ser
ENST00000697316.1:n.1848T>G
ENST00000697317.1:n.1837T>G
ENST00000697318.1:n.1839T>G
ENST00000265433.8:c.1727T>G MANE Select	ENSP00000265433.4:p.Ile576Ser
ENST00000265433.7:c.1727T>G	ENSP00000265433.3:p.Ile576Ser
ENST00000396252.6:c.*1600T>G	ENSP00000379551.2:n.*1600T>G
ENST00000409330.5:c.1481T>G	ENSP00000386924.1:p.Ile494Ser
NM_001024688.2:c.1481T>G	NP_001019859.1:p.Ile494Ser
NM_002485.4:c.1727T>G , LRG_158t1:c.1727T>G	NP_002476.2:p.Ile576Ser
XM_011517044.1:c.1703T>G	XP_011515346.1:p.Ile568Ser
XM_011517045.1:c.1481T>G	XP_011515347.1:p.Ile494Ser
XR_928335.1:n.1866T>G
XM_017013460.1:c.848T>G	XP_016868949.1:p.Ile283Ser
XM_017013462.2:c.848T>G	XP_016868951.1:p.Ile283Ser
XM_024447163.1:c.1481T>G	XP_024302931.1:p.Ile494Ser
XM_024447164.1:c.1481T>G	XP_024302932.1:p.Ile494Ser
XM_024447165.1:c.848T>G	XP_024302933.1:p.Ile283Ser
NM_002485.5:c.1727T>G MANE Select	NP_002476.2:p.Ile576Ser
NM_001024688.3:c.1481T>G	NP_001019859.1:p.Ile494Ser