Canonical Allele Identifier: CA1801470069
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89982815A= , CM000670.2:g.89982815A= GRCh38
NC_000008.10:g.90995043A= , CM000670.1:g.90995043A= GRCh37
NC_000008.9:g.91064219A= NCBI36
NG_008860.1:g.6857T= , LRG_158:g.6857T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.182T=
ENST00000517337.2:c.-219T= ENSP00000429971.2:n.-219T=
ENST00000523444.2:c.-219T= ENSP00000428252.2:n.-219T=
ENST00000697292.1:c.78T= ENSP00000513229.1:p.Val26=
ENST00000697293.1:c.78T= ENSP00000513230.1:p.Val26=
ENST00000697294.1:c.78T= ENSP00000513231.1:p.Val26=
ENST00000697295.1:c.37+1710T= ENSP00000513232.1:n.37+1710T=
ENST00000697296.1:c.78T= ENSP00000513233.1:p.Val26=
ENST00000697297.1:n.184T=
ENST00000697298.1:c.-219T= ENSP00000513234.1:n.-219T=
ENST00000697299.1:c.-75-1292T= ENSP00000513235.1:n.-75-1292T=
ENST00000697300.1:c.-219T= ENSP00000513236.1:n.-219T=
ENST00000697301.1:c.-219T= ENSP00000513237.1:n.-219T=
ENST00000697302.1:c.78T= ENSP00000513238.1:p.Val26=
ENST00000697303.1:c.78T= ENSP00000513239.1:p.Val26=
ENST00000697304.1:c.78T= ENSP00000513240.1:p.Val26=
ENST00000697306.1:c.78T= ENSP00000513241.1:p.Val26=
ENST00000697307.1:c.78T= ENSP00000513242.1:p.Val26=
ENST00000697308.1:c.78T= ENSP00000513243.1:p.Val26=
ENST00000697309.1:c.78T= ENSP00000513244.1:p.Val26=
ENST00000697310.1:c.78T= ENSP00000513245.1:p.Val26=
ENST00000697311.1:c.78T= ENSP00000513246.1:p.Val26=
ENST00000697312.1:c.78T= ENSP00000513247.1:p.Val26=
ENST00000697313.1:n.190T=
ENST00000697314.1:n.190T=
ENST00000697315.1:c.78T= ENSP00000513248.1:p.Val26=
ENST00000697316.1:n.199T=
ENST00000697317.1:n.188T=
ENST00000697318.1:n.190T=
ENST00000265433.8:c.78T= MANE Select ENSP00000265433.4:p.Val26=
ENST00000265433.7:c.78T= ENSP00000265433.3:p.Val26=
ENST00000396252.6:c.78T= ENSP00000379551.2:p.Val26=
ENST00000409330.5:c.-169T= ENSP00000386924.1:n.-169T=
ENST00000494804.1:n.182T=
ENST00000517337.1:c.-219T= ENSP00000429971.1:n.-219T=
ENST00000519426.5:c.78T= ENSP00000430983.1:p.Val26=
ENST00000523444.1:c.78T= ENSP00000428252.1:p.Val26=
NM_001024688.2:c.-219T= NP_001019859.1:n.-219T=
NM_002485.4:c.78T= , LRG_158t1:c.78T= NP_002476.2:p.Val26=
XM_011517044.1:c.54T= XP_011515346.1:p.Val18=
XM_011517045.1:c.-219T= XP_011515347.1:n.-219T=
XM_011517046.1:c.78T= XP_011515348.1:p.Val26=
XR_928335.1:n.215T=
XM_017013460.1:c.-942T= XP_016868949.1:n.-942T=
XM_017013462.2:c.-748T= XP_016868951.1:n.-748T=
XM_024447163.1:c.-169T= XP_024302931.1:n.-169T=
XM_024447165.1:c.-892T= XP_024302933.1:n.-892T=
NM_002485.5:c.78T= MANE Select NP_002476.2:p.Val26=
NM_001024688.3:c.-219T= NP_001019859.1:n.-219T=