Canonical Allele Identifier: CA2507526705

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89982555del , CM000670.2:g.89982555del	GRCh38
NC_000008.10:g.90994783del , CM000670.1:g.90994783del	GRCh37
NC_000008.9:g.91063959del	NCBI36
NG_008860.1:g.7118del , LRG_158:g.7118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.443del
ENST00000517337.2:c.-126+168del	ENSP00000429971.2:n.-126+168del
ENST00000523444.2:c.-126+168del	ENSP00000428252.2:n.-126+168del
ENST00000697292.1:c.171+168del	ENSP00000513229.1:n.171+168del
ENST00000697293.1:c.171+168del	ENSP00000513230.1:n.171+168del
ENST00000697294.1:c.171+168del	ENSP00000513231.1:n.171+168del
ENST00000697295.1:c.37+1971del	ENSP00000513232.1:n.37+1971del
ENST00000697296.1:c.171+168del	ENSP00000513233.1:n.171+168del
ENST00000697297.1:n.445del
ENST00000697298.1:c.-126+168del	ENSP00000513234.1:n.-126+168del
ENST00000697299.1:c.-75-1031del	ENSP00000513235.1:n.-75-1031del
ENST00000697300.1:c.-126+168del	ENSP00000513236.1:n.-126+168del
ENST00000697301.1:c.-126+168del	ENSP00000513237.1:n.-126+168del
ENST00000697302.1:c.171+168del	ENSP00000513238.1:n.171+168del
ENST00000697303.1:c.171+168del	ENSP00000513239.1:n.171+168del
ENST00000697304.1:c.171+168del	ENSP00000513240.1:n.171+168del
ENST00000697306.1:c.171+168del	ENSP00000513241.1:n.171+168del
ENST00000697307.1:c.171+168del	ENSP00000513242.1:n.171+168del
ENST00000697308.1:c.171+168del	ENSP00000513243.1:n.171+168del
ENST00000697309.1:c.171+168del	ENSP00000513244.1:n.171+168del
ENST00000697310.1:c.171+168del	ENSP00000513245.1:n.171+168del
ENST00000697311.1:c.171+168del	ENSP00000513246.1:n.171+168del
ENST00000697312.1:c.171+168del	ENSP00000513247.1:n.171+168del
ENST00000697313.1:n.451del
ENST00000697314.1:n.451del
ENST00000697315.1:c.171+168del	ENSP00000513248.1:n.171+168del
ENST00000697316.1:n.292+168del
ENST00000697317.1:n.281+168del
ENST00000697318.1:n.283+168del
ENST00000265433.8:c.171+168del MANE Select	ENSP00000265433.4:n.171+168del
ENST00000265433.7:c.171+168del	ENSP00000265433.3:n.171+168del
ENST00000396252.6:c.171+168del	ENSP00000379551.2:n.171+168del
ENST00000409330.5:c.-76+168del	ENSP00000386924.1:n.-76+168del
ENST00000494804.1:n.443del
ENST00000517337.1:c.-126+168del	ENSP00000429971.1:n.-126+168del
ENST00000519426.5:c.171+168del	ENSP00000430983.1:n.171+168del
ENST00000523444.1:c.171+168del	ENSP00000428252.1:n.171+168del
NM_001024688.2:c.-126+168del	NP_001019859.1:n.-126+168del
NM_002485.4:c.171+168del , LRG_158t1:c.171+168del	NP_002476.2:n.171+168del
XM_011517044.1:c.147+168del	XP_011515346.1:n.147+168del
XM_011517045.1:c.-126+168del	XP_011515347.1:n.-126+168del
XM_011517046.1:c.171+168del	XP_011515348.1:n.171+168del
XR_928335.1:n.308+168del
XM_017013460.1:c.-849+168del	XP_016868949.1:n.-849+168del
XM_017013462.2:c.-655+168del	XP_016868951.1:n.-655+168del
XM_024447163.1:c.-76+168del	XP_024302931.1:n.-76+168del
XM_024447165.1:c.-799+168del	XP_024302933.1:n.-799+168del
NM_002485.5:c.171+168del MANE Select	NP_002476.2:n.171+168del
NM_001024688.3:c.-126+168del	NP_001019859.1:n.-126+168del