Canonical Allele Identifier: CA371658295

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90982617G>T (hg19) ; chr8:g.89970389G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970389G>T , CM000670.2:g.89970389G>T	GRCh38
NC_000008.10:g.90982617G>T , CM000670.1:g.90982617G>T	GRCh37
NC_000008.9:g.91051793G>T	NCBI36
NG_008860.1:g.19283C>A , LRG_158:g.19283C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2173C>A
ENST00000517337.2:c.625C>A	ENSP00000429971.2:p.Gln209Lys
ENST00000523444.2:c.625C>A	ENSP00000428252.2:p.Gln209Lys
ENST00000697292.1:c.871C>A	ENSP00000513229.1:p.Gln291Lys
ENST00000697293.1:c.871C>A	ENSP00000513230.1:p.Gln291Lys
ENST00000697294.1:c.*482C>A	ENSP00000513231.1:n.*482C>A
ENST00000697295.1:c.*180C>A	ENSP00000513232.1:n.*180C>A
ENST00000697296.1:c.*539C>A	ENSP00000513233.1:n.*539C>A
ENST00000697297.1:n.2656C>A
ENST00000697298.1:c.625C>A	ENSP00000513234.1:p.Gln209Lys
ENST00000697299.1:c.625C>A	ENSP00000513235.1:p.Gln209Lys
ENST00000697300.1:c.*475C>A	ENSP00000513236.1:n.*475C>A
ENST00000697301.1:c.*392C>A	ENSP00000513237.1:n.*392C>A
ENST00000697302.1:c.*392C>A	ENSP00000513238.1:n.*392C>A
ENST00000697303.1:c.*475C>A	ENSP00000513239.1:n.*475C>A
ENST00000697304.1:c.585-5882C>A	ENSP00000513240.1:n.585-5882C>A
ENST00000697306.1:c.480+10345C>A	ENSP00000513241.1:n.480+10345C>A
ENST00000697307.1:c.871C>A	ENSP00000513242.1:p.Gln291Lys
ENST00000697308.1:c.871C>A	ENSP00000513243.1:p.Gln291Lys
ENST00000697309.1:c.871C>A	ENSP00000513244.1:p.Gln291Lys
ENST00000697310.1:c.871C>A	ENSP00000513245.1:p.Gln291Lys
ENST00000697311.1:c.871C>A	ENSP00000513246.1:p.Gln291Lys
ENST00000697312.1:c.*269C>A	ENSP00000513247.1:n.*269C>A
ENST00000697313.1:n.2662C>A
ENST00000697314.1:n.2662C>A
ENST00000697315.1:c.871C>A	ENSP00000513248.1:p.Gln291Lys
ENST00000697316.1:n.992C>A
ENST00000697317.1:n.981C>A
ENST00000697318.1:n.983C>A
ENST00000265433.8:c.871C>A MANE Select	ENSP00000265433.4:p.Gln291Lys
ENST00000265433.7:c.871C>A	ENSP00000265433.3:p.Gln291Lys
ENST00000396252.6:c.*744C>A	ENSP00000379551.2:n.*744C>A
ENST00000409330.5:c.625C>A	ENSP00000386924.1:p.Gln209Lys
NM_001024688.2:c.625C>A	NP_001019859.1:p.Gln209Lys
NM_002485.4:c.871C>A , LRG_158t1:c.871C>A	NP_002476.2:p.Gln291Lys
XM_011517044.1:c.847C>A	XP_011515346.1:p.Gln283Lys
XM_011517045.1:c.625C>A	XP_011515347.1:p.Gln209Lys
XM_011517046.1:c.871C>A	XP_011515348.1:p.Gln291Lys
XR_928335.1:n.1008C>A
XM_017013460.1:c.-9C>A	XP_016868949.1:n.-9C>A
XM_017013462.2:c.-9C>A	XP_016868951.1:n.-9C>A
XM_024447163.1:c.625C>A	XP_024302931.1:p.Gln209Lys
XM_024447164.1:c.625C>A	XP_024302932.1:p.Gln209Lys
XM_024447165.1:c.-9C>A	XP_024302933.1:n.-9C>A
NM_002485.5:c.871C>A MANE Select	NP_002476.2:p.Gln291Lys
NM_001024688.3:c.625C>A	NP_001019859.1:p.Gln209Lys