Canonical Allele Identifier: CA10578766

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89955280G>C , CM000670.2:g.89955280G>C	GRCh38
NC_000008.10:g.90967508G>C , CM000670.1:g.90967508G>C	GRCh37
NC_000008.9:g.91036684G>C	NCBI36
NG_008860.1:g.34392C>G , LRG_158:g.34392C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2699+3C>G
ENST00000517337.2:c.1151+3C>G	ENSP00000429971.2:n.1151+3C>G
ENST00000523444.2:c.1151+3C>G	ENSP00000428252.2:n.1151+3C>G
ENST00000697292.1:c.1397+3C>G	ENSP00000513229.1:n.1397+3C>G
ENST00000697293.1:c.1397+3C>G	ENSP00000513230.1:n.1397+3C>G
ENST00000697294.1:c.*1008+3C>G	ENSP00000513231.1:n.*1008+3C>G
ENST00000697295.1:c.*706+3C>G	ENSP00000513232.1:n.*706+3C>G
ENST00000697296.1:c.*1065+3C>G	ENSP00000513233.1:n.*1065+3C>G
ENST00000697297.1:n.3182+3C>G
ENST00000697298.1:c.1151+3C>G	ENSP00000513234.1:n.1151+3C>G
ENST00000697299.1:c.1151+3C>G	ENSP00000513235.1:n.1151+3C>G
ENST00000697300.1:c.*1001+3C>G	ENSP00000513236.1:n.*1001+3C>G
ENST00000697301.1:c.*918+3C>G	ENSP00000513237.1:n.*918+3C>G
ENST00000697302.1:c.*918+3C>G	ENSP00000513238.1:n.*918+3C>G
ENST00000697303.1:c.*1001+3C>G	ENSP00000513239.1:n.*1001+3C>G
ENST00000697304.1:c.1085+3C>G	ENSP00000513240.1:n.1085+3C>G
ENST00000697306.1:c.*397+3C>G	ENSP00000513241.1:n.*397+3C>G
ENST00000697307.1:c.1397+3C>G	ENSP00000513242.1:n.1397+3C>G
ENST00000697308.1:c.1397+3C>G	ENSP00000513243.1:n.1397+3C>G
ENST00000697309.1:c.1397+3C>G	ENSP00000513244.1:n.1397+3C>G
ENST00000697310.1:c.1397+3C>G	ENSP00000513245.1:n.1397+3C>G
ENST00000697311.1:c.1397+3C>G	ENSP00000513246.1:n.1397+3C>G
ENST00000697312.1:c.*795+3C>G	ENSP00000513247.1:n.*795+3C>G
ENST00000697313.1:n.2687+15084C>G
ENST00000697314.1:n.3188+3C>G
ENST00000697315.1:c.1397+3C>G	ENSP00000513248.1:n.1397+3C>G
ENST00000697316.1:n.1518+3C>G
ENST00000697317.1:n.1507+3C>G
ENST00000697318.1:n.1509+3C>G
ENST00000265433.8:c.1397+3C>G MANE Select	ENSP00000265433.4:n.1397+3C>G
ENST00000265433.7:c.1397+3C>G	ENSP00000265433.3:n.1397+3C>G
ENST00000396252.6:c.*1270+3C>G	ENSP00000379551.2:n.*1270+3C>G
ENST00000409330.5:c.1151+3C>G	ENSP00000386924.1:n.1151+3C>G
NM_001024688.2:c.1151+3C>G	NP_001019859.1:n.1151+3C>G
NM_002485.4:c.1397+3C>G , LRG_158t1:c.1397+3C>G	NP_002476.2:n.1397+3C>G
XM_011517044.1:c.1373+3C>G	XP_011515346.1:n.1373+3C>G
XM_011517045.1:c.1151+3C>G	XP_011515347.1:n.1151+3C>G
XM_011517046.1:c.1395+5C>G	XP_011515348.1:n.1395+5C>G
XR_928335.1:n.1533+4C>G
XM_017013460.1:c.518+3C>G	XP_016868949.1:n.518+3C>G
XM_017013462.2:c.518+3C>G	XP_016868951.1:n.518+3C>G
XM_024447163.1:c.1151+3C>G	XP_024302931.1:n.1151+3C>G
XM_024447164.1:c.1151+3C>G	XP_024302932.1:n.1151+3C>G
XM_024447165.1:c.518+3C>G	XP_024302933.1:n.518+3C>G
NM_002485.5:c.1397+3C>G MANE Select	NP_002476.2:n.1397+3C>G
NM_001024688.3:c.1151+3C>G	NP_001019859.1:n.1151+3C>G