Canonical Allele Identifier: CA2781235904

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89971048del , CM000670.2:g.89971048del	GRCh38
NC_000008.10:g.90983276del , CM000670.1:g.90983276del	GRCh37
NC_000008.9:g.91052452del	NCBI36
NG_008860.1:g.18624del , LRG_158:g.18624del

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.2004+125del
ENST00000517337.2:c.456+125del	ENSP00000429971.2:n.456+125del
ENST00000523444.2:c.456+125del	ENSP00000428252.2:n.456+125del
ENST00000697292.1:c.702+125del	ENSP00000513229.1:n.702+125del
ENST00000697293.1:c.702+125del	ENSP00000513230.1:n.702+125del
ENST00000697294.1:c.*313+125del	ENSP00000513231.1:n.*313+125del
ENST00000697295.1:c.*11+125del	ENSP00000513232.1:n.*11+125del
ENST00000697296.1:c.*370+125del	ENSP00000513233.1:n.*370+125del
ENST00000697297.1:n.2487+125del
ENST00000697298.1:c.456+125del	ENSP00000513234.1:n.456+125del
ENST00000697299.1:c.456+125del	ENSP00000513235.1:n.456+125del
ENST00000697300.1:c.*306+125del	ENSP00000513236.1:n.*306+125del
ENST00000697301.1:c.*223+125del	ENSP00000513237.1:n.*223+125del
ENST00000697302.1:c.*223+125del	ENSP00000513238.1:n.*223+125del
ENST00000697303.1:c.*306+125del	ENSP00000513239.1:n.*306+125del
ENST00000697304.1:c.585-6541del	ENSP00000513240.1:n.585-6541del
ENST00000697306.1:c.480+9686del	ENSP00000513241.1:n.480+9686del
ENST00000697307.1:c.702+125del	ENSP00000513242.1:n.702+125del
ENST00000697308.1:c.702+125del	ENSP00000513243.1:n.702+125del
ENST00000697309.1:c.702+125del	ENSP00000513244.1:n.702+125del
ENST00000697310.1:c.702+125del	ENSP00000513245.1:n.702+125del
ENST00000697311.1:c.702+125del	ENSP00000513246.1:n.702+125del
ENST00000697312.1:c.*100+125del	ENSP00000513247.1:n.*100+125del
ENST00000697313.1:n.2493+125del
ENST00000697314.1:n.2493+125del
ENST00000697315.1:c.702+125del	ENSP00000513248.1:n.702+125del
ENST00000697316.1:n.823+125del
ENST00000697317.1:n.812+125del
ENST00000697318.1:n.814+125del
ENST00000265433.8:c.702+125del MANE Select	ENSP00000265433.4:n.702+125del
ENST00000265433.7:c.702+125del	ENSP00000265433.3:n.702+125del
ENST00000396252.6:c.*575+125del	ENSP00000379551.2:n.*575+125del
ENST00000409330.5:c.456+125del	ENSP00000386924.1:n.456+125del
ENST00000517772.5:c.456+125del	ENSP00000428717.1:n.456+125del
ENST00000519426.5:c.438+125del	ENSP00000430983.1:n.438+125del
NM_001024688.2:c.456+125del	NP_001019859.1:n.456+125del
NM_002485.4:c.702+125del , LRG_158t1:c.702+125del	NP_002476.2:n.702+125del
XM_011517044.1:c.678+125del	XP_011515346.1:n.678+125del
XM_011517045.1:c.456+125del	XP_011515347.1:n.456+125del
XM_011517046.1:c.702+125del	XP_011515348.1:n.702+125del
XR_928335.1:n.839+125del
XM_017013460.1:c.-178+125del	XP_016868949.1:n.-178+125del
XM_017013462.2:c.-178+125del	XP_016868951.1:n.-178+125del
XM_024447163.1:c.456+125del	XP_024302931.1:n.456+125del
XM_024447164.1:c.456+125del	XP_024302932.1:n.456+125del
XM_024447165.1:c.-178+125del	XP_024302933.1:n.-178+125del
NM_002485.5:c.702+125del MANE Select	NP_002476.2:n.702+125del
NM_001024688.3:c.456+125del	NP_001019859.1:n.456+125del