Canonical Allele Identifier: CA371655250

Gene: NBN

Linked Data

• ClinVar Variation Id: 1801526
• ClinVar RCV Id: RCV003164559
• MyVariant Identifiers: chr8:g.90965600C>A (hg19) ; chr8:g.89953372C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953372C>A , CM000670.2:g.89953372C>A	GRCh38
NC_000008.10:g.90965600C>A , CM000670.1:g.90965600C>A	GRCh37
NC_000008.9:g.91034776C>A	NCBI36
NG_008860.1:g.36300G>T , LRG_158:g.36300G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3019G>T
ENST00000517337.2:c.1471G>T	ENSP00000429971.2:p.Glu491Ter
ENST00000523444.2:c.1471G>T	ENSP00000428252.2:p.Glu491Ter
ENST00000697292.1:c.1717G>T	ENSP00000513229.1:p.Glu573Ter
ENST00000697293.1:c.1717G>T	ENSP00000513230.1:p.Glu573Ter
ENST00000697294.1:c.*1328G>T	ENSP00000513231.1:n.*1328G>T
ENST00000697295.1:c.*1026G>T	ENSP00000513232.1:n.*1026G>T
ENST00000697296.1:c.*1385G>T	ENSP00000513233.1:n.*1385G>T
ENST00000697297.1:n.3502G>T
ENST00000697298.1:c.1471G>T	ENSP00000513234.1:p.Glu491Ter
ENST00000697299.1:c.1471G>T	ENSP00000513235.1:p.Glu491Ter
ENST00000697300.1:c.*1321G>T	ENSP00000513236.1:n.*1321G>T
ENST00000697301.1:c.*1238G>T	ENSP00000513237.1:n.*1238G>T
ENST00000697302.1:c.*1238G>T	ENSP00000513238.1:n.*1238G>T
ENST00000697303.1:c.*1321G>T	ENSP00000513239.1:n.*1321G>T
ENST00000697304.1:c.1405G>T	ENSP00000513240.1:p.Glu469Ter
ENST00000697306.1:c.*717G>T	ENSP00000513241.1:n.*717G>T
ENST00000697307.1:c.1717G>T	ENSP00000513242.1:p.Glu573Ter
ENST00000697308.1:c.1717G>T	ENSP00000513243.1:p.Glu573Ter
ENST00000697309.1:c.1717G>T	ENSP00000513244.1:p.Glu573Ter
ENST00000697310.1:c.1717G>T	ENSP00000513245.1:p.Glu573Ter
ENST00000697311.1:c.1717G>T	ENSP00000513246.1:p.Glu573Ter
ENST00000697312.1:c.*1115G>T	ENSP00000513247.1:n.*1115G>T
ENST00000697313.1:n.2687+16992G>T
ENST00000697314.1:n.3508G>T
ENST00000697315.1:c.1717G>T	ENSP00000513248.1:p.Glu573Ter
ENST00000697316.1:n.1838G>T
ENST00000697317.1:n.1827G>T
ENST00000697318.1:n.1829G>T
ENST00000265433.8:c.1717G>T MANE Select	ENSP00000265433.4:p.Glu573Ter
ENST00000265433.7:c.1717G>T	ENSP00000265433.3:p.Glu573Ter
ENST00000396252.6:c.*1590G>T	ENSP00000379551.2:n.*1590G>T
ENST00000409330.5:c.1471G>T	ENSP00000386924.1:p.Glu491Ter
NM_001024688.2:c.1471G>T	NP_001019859.1:p.Glu491Ter
NM_002485.4:c.1717G>T , LRG_158t1:c.1717G>T	NP_002476.2:p.Glu573Ter
XM_011517044.1:c.1693G>T	XP_011515346.1:p.Glu565Ter
XM_011517045.1:c.1471G>T	XP_011515347.1:p.Glu491Ter
XR_928335.1:n.1856G>T
XM_017013460.1:c.838G>T	XP_016868949.1:p.Glu280Ter
XM_017013462.2:c.838G>T	XP_016868951.1:p.Glu280Ter
XM_024447163.1:c.1471G>T	XP_024302931.1:p.Glu491Ter
XM_024447164.1:c.1471G>T	XP_024302932.1:p.Glu491Ter
XM_024447165.1:c.838G>T	XP_024302933.1:p.Glu280Ter
NM_002485.5:c.1717G>T MANE Select	NP_002476.2:p.Glu573Ter
NM_001024688.3:c.1471G>T	NP_001019859.1:p.Glu491Ter