Canonical Allele Identifier: CA10577371
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89984556C>T , CM000670.2:g.89984556C>T GRCh38
NC_000008.10:g.90996784C>T , CM000670.1:g.90996784C>T GRCh37
NC_000008.9:g.91065960C>T NCBI36
NG_008860.1:g.5116G>A , LRG_158:g.5116G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.110G>A
ENST00000523444.2:c.-291G>A ENSP00000428252.2:n.-291G>A
ENST00000697292.1:c.6G>A ENSP00000513229.1:p.Trp2Ter
ENST00000697293.1:c.6G>A ENSP00000513230.1:p.Trp2Ter
ENST00000697294.1:c.6G>A ENSP00000513231.1:p.Trp2Ter
ENST00000697295.1:c.6G>A ENSP00000513232.1:p.Trp2Ter
ENST00000697296.1:c.6G>A ENSP00000513233.1:p.Trp2Ter
ENST00000697297.1:n.112G>A
ENST00000697298.1:c.-474G>A ENSP00000513234.1:n.-474G>A
ENST00000697299.1:c.-107G>A ENSP00000513235.1:n.-107G>A
ENST00000697300.1:c.-291G>A ENSP00000513236.1:n.-291G>A
ENST00000697301.1:c.-291G>A ENSP00000513237.1:n.-291G>A
ENST00000697302.1:c.6G>A ENSP00000513238.1:p.Trp2Ter
ENST00000697303.1:c.6G>A ENSP00000513239.1:p.Trp2Ter
ENST00000697304.1:c.6G>A ENSP00000513240.1:p.Trp2Ter
ENST00000697306.1:c.6G>A ENSP00000513241.1:p.Trp2Ter
ENST00000697307.1:c.6G>A ENSP00000513242.1:p.Trp2Ter
ENST00000697308.1:c.6G>A ENSP00000513243.1:p.Trp2Ter
ENST00000697309.1:c.6G>A ENSP00000513244.1:p.Trp2Ter
ENST00000697310.1:c.6G>A ENSP00000513245.1:p.Trp2Ter
ENST00000697311.1:c.6G>A ENSP00000513246.1:p.Trp2Ter
ENST00000697312.1:c.6G>A ENSP00000513247.1:p.Trp2Ter
ENST00000697313.1:n.118G>A
ENST00000697314.1:n.118G>A
ENST00000697315.1:c.6G>A ENSP00000513248.1:p.Trp2Ter
ENST00000697316.1:n.127G>A
ENST00000697317.1:n.116G>A
ENST00000697318.1:n.118G>A
ENST00000265433.8:c.6G>A MANE Select ENSP00000265433.4:p.Trp2Ter
ENST00000265433.7:c.6G>A ENSP00000265433.3:p.Trp2Ter
ENST00000396252.6:c.6G>A ENSP00000379551.2:p.Trp2Ter
ENST00000494804.1:n.110G>A
ENST00000519426.5:c.6G>A ENSP00000430983.1:p.Trp2Ter
ENST00000523444.1:c.6G>A ENSP00000428252.1:p.Trp2Ter
NM_001024688.2:c.-291G>A NP_001019859.1:n.-291G>A
NM_002485.4:c.6G>A , LRG_158t1:c.6G>A NP_002476.2:p.Trp2Ter
XM_011517046.1:c.6G>A XP_011515348.1:p.Trp2Ter
XR_928335.1:n.143G>A
XM_017013460.1:c.-1014G>A XP_016868949.1:n.-1014G>A
XM_017013462.2:c.-820G>A XP_016868951.1:n.-820G>A
XM_024447165.1:c.-964G>A XP_024302933.1:n.-964G>A
NM_002485.5:c.6G>A MANE Select NP_002476.2:p.Trp2Ter
NM_001024688.3:c.-291G>A NP_001019859.1:n.-291G>A