Canonical Allele Identifier: CA1801471072

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89984535_89984536delinsGC , CM000670.2:g.89984535_89984536delinsGC	GRCh38
NC_000008.10:g.90996763_90996764delinsGC , CM000670.1:g.90996763_90996764delinsGC	GRCh37
NC_000008.9:g.91065939_91065940delinsGC	NCBI36
NG_008860.1:g.5136_5137delinsGC , LRG_158:g.5136_5137delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.130_131delinsGC
ENST00000523444.2:c.-271_-270delinsGC	ENSP00000428252.2:n.-271_-270delinsGC
ENST00000697292.1:c.26_27delinsGC	ENSP00000513229.1:p.Gly9=
ENST00000697293.1:c.26_27delinsGC	ENSP00000513230.1:p.Gly9=
ENST00000697294.1:c.26_27delinsGC	ENSP00000513231.1:p.Gly9=
ENST00000697295.1:c.26_27delinsGC	ENSP00000513232.1:p.Gly9=
ENST00000697296.1:c.26_27delinsGC	ENSP00000513233.1:p.Gly9=
ENST00000697297.1:n.132_133delinsGC
ENST00000697298.1:c.-454_-453delinsGC	ENSP00000513234.1:n.-454_-453delinsGC
ENST00000697299.1:c.-87_-86delinsGC	ENSP00000513235.1:n.-87_-86delinsGC
ENST00000697300.1:c.-271_-270delinsGC	ENSP00000513236.1:n.-271_-270delinsGC
ENST00000697301.1:c.-271_-270delinsGC	ENSP00000513237.1:n.-271_-270delinsGC
ENST00000697302.1:c.26_27delinsGC	ENSP00000513238.1:p.Gly9=
ENST00000697303.1:c.26_27delinsGC	ENSP00000513239.1:p.Gly9=
ENST00000697304.1:c.26_27delinsGC	ENSP00000513240.1:p.Gly9=
ENST00000697306.1:c.26_27delinsGC	ENSP00000513241.1:p.Gly9=
ENST00000697307.1:c.26_27delinsGC	ENSP00000513242.1:p.Gly9=
ENST00000697308.1:c.26_27delinsGC	ENSP00000513243.1:p.Gly9=
ENST00000697309.1:c.26_27delinsGC	ENSP00000513244.1:p.Gly9=
ENST00000697310.1:c.26_27delinsGC	ENSP00000513245.1:p.Gly9=
ENST00000697311.1:c.26_27delinsGC	ENSP00000513246.1:p.Gly9=
ENST00000697312.1:c.26_27delinsGC	ENSP00000513247.1:p.Gly9=
ENST00000697313.1:n.138_139delinsGC
ENST00000697314.1:n.138_139delinsGC
ENST00000697315.1:c.26_27delinsGC	ENSP00000513248.1:p.Gly9=
ENST00000697316.1:n.147_148delinsGC
ENST00000697317.1:n.136_137delinsGC
ENST00000697318.1:n.138_139delinsGC
ENST00000265433.8:c.26_27delinsGC MANE Select	ENSP00000265433.4:p.Gly9=
ENST00000265433.7:c.26_27delinsGC	ENSP00000265433.3:p.Gly9=
ENST00000396252.6:c.26_27delinsGC	ENSP00000379551.2:p.Gly9=
ENST00000494804.1:n.130_131delinsGC
ENST00000519426.5:c.26_27delinsGC	ENSP00000430983.1:p.Gly9=
ENST00000523444.1:c.26_27delinsGC	ENSP00000428252.1:p.Gly9=
NM_001024688.2:c.-271_-270delinsGC	NP_001019859.1:n.-271_-270delinsGC
NM_002485.4:c.26_27delinsGC , LRG_158t1:c.26_27delinsGC	NP_002476.2:p.Gly9=
XM_011517046.1:c.26_27delinsGC	XP_011515348.1:p.Gly9=
XR_928335.1:n.163_164delinsGC
XM_017013460.1:c.-994_-993delinsGC	XP_016868949.1:n.-994_-993delinsGC
XM_017013462.2:c.-800_-799delinsGC	XP_016868951.1:n.-800_-799delinsGC
XM_024447165.1:c.-944_-943delinsGC	XP_024302933.1:n.-944_-943delinsGC
NM_002485.5:c.26_27delinsGC MANE Select	NP_002476.2:p.Gly9=
NM_001024688.3:c.-271_-270delinsGC	NP_001019859.1:n.-271_-270delinsGC