Canonical Allele Identifier: CA4802721

Gene: NBN

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953672G>T , CM000670.2:g.89953672G>T	GRCh38
NC_000008.10:g.90965900G>T , CM000670.1:g.90965900G>T	GRCh37
NC_000008.9:g.91035076G>T	NCBI36
NG_008860.1:g.36000C>A , LRG_158:g.36000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2719C>A
ENST00000517337.2:c.1171C>A	ENSP00000429971.2:p.Gln391Lys
ENST00000523444.2:c.1171C>A	ENSP00000428252.2:p.Gln391Lys
ENST00000697292.1:c.1417C>A	ENSP00000513229.1:p.Gln473Lys
ENST00000697293.1:c.1417C>A	ENSP00000513230.1:p.Gln473Lys
ENST00000697294.1:c.*1028C>A	ENSP00000513231.1:n.*1028C>A
ENST00000697295.1:c.*726C>A	ENSP00000513232.1:n.*726C>A
ENST00000697296.1:c.*1085C>A	ENSP00000513233.1:n.*1085C>A
ENST00000697297.1:n.3202C>A
ENST00000697298.1:c.1171C>A	ENSP00000513234.1:p.Gln391Lys
ENST00000697299.1:c.1171C>A	ENSP00000513235.1:p.Gln391Lys
ENST00000697300.1:c.*1021C>A	ENSP00000513236.1:n.*1021C>A
ENST00000697301.1:c.*938C>A	ENSP00000513237.1:n.*938C>A
ENST00000697302.1:c.*938C>A	ENSP00000513238.1:n.*938C>A
ENST00000697303.1:c.*1021C>A	ENSP00000513239.1:n.*1021C>A
ENST00000697304.1:c.1105C>A	ENSP00000513240.1:p.Gln369Lys
ENST00000697306.1:c.*417C>A	ENSP00000513241.1:n.*417C>A
ENST00000697307.1:c.1417C>A	ENSP00000513242.1:p.Gln473Lys
ENST00000697308.1:c.1417C>A	ENSP00000513243.1:p.Gln473Lys
ENST00000697309.1:c.1417C>A	ENSP00000513244.1:p.Gln473Lys
ENST00000697310.1:c.1417C>A	ENSP00000513245.1:p.Gln473Lys
ENST00000697311.1:c.1417C>A	ENSP00000513246.1:p.Gln473Lys
ENST00000697312.1:c.*815C>A	ENSP00000513247.1:n.*815C>A
ENST00000697313.1:n.2687+16692C>A
ENST00000697314.1:n.3208C>A
ENST00000697315.1:c.1417C>A	ENSP00000513248.1:p.Gln473Lys
ENST00000697316.1:n.1538C>A
ENST00000697317.1:n.1527C>A
ENST00000697318.1:n.1529C>A
ENST00000265433.8:c.1417C>A MANE Select	ENSP00000265433.4:p.Gln473Lys
ENST00000265433.7:c.1417C>A	ENSP00000265433.3:p.Gln473Lys
ENST00000396252.6:c.*1290C>A	ENSP00000379551.2:n.*1290C>A
ENST00000409330.5:c.1171C>A	ENSP00000386924.1:p.Gln391Lys
NM_001024688.2:c.1171C>A	NP_001019859.1:p.Gln391Lys
NM_002485.4:c.1417C>A , LRG_158t1:c.1417C>A	NP_002476.2:p.Gln473Lys
XM_011517044.1:c.1393C>A	XP_011515346.1:p.Gln465Lys
XM_011517045.1:c.1171C>A	XP_011515347.1:p.Gln391Lys
XM_011517046.1:c.*8C>A	XP_011515348.1:n.*8C>A
XR_928335.1:n.1556C>A
XM_017013460.1:c.538C>A	XP_016868949.1:p.Gln180Lys
XM_017013462.2:c.538C>A	XP_016868951.1:p.Gln180Lys
XM_024447163.1:c.1171C>A	XP_024302931.1:p.Gln391Lys
XM_024447164.1:c.1171C>A	XP_024302932.1:p.Gln391Lys
XM_024447165.1:c.538C>A	XP_024302933.1:p.Gln180Lys
NM_002485.5:c.1417C>A MANE Select	NP_002476.2:p.Gln473Lys
NM_001024688.3:c.1171C>A	NP_001019859.1:p.Gln391Lys