Canonical Allele Identifier: CA1801469846
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89982701_89982706delinsGAAATA , CM000670.2:g.89982701_89982706delinsGAAATA GRCh38
NC_000008.10:g.90994929_90994934delinsGAAATA , CM000670.1:g.90994929_90994934delinsGAAATA GRCh37
NC_000008.9:g.91064105_91064110delinsGAAATA NCBI36
NG_008860.1:g.6966_6971delinsTATTTC , LRG_158:g.6966_6971delinsTATTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000494804.2:n.291_296delinsTATTTC
ENST00000517337.2:c.-126+16_-126+21delinsTATTTC ENSP00000429971.2:n.-126+16_-126+21delins...
ENST00000523444.2:c.-126+16_-126+21delinsTATTTC ENSP00000428252.2:n.-126+16_-126+21delins...
ENST00000697292.1:c.171+16_171+21delinsTATTTC ENSP00000513229.1:n.171+16_171+21delinsTA...
ENST00000697293.1:c.171+16_171+21delinsTATTTC ENSP00000513230.1:n.171+16_171+21delinsTA...
ENST00000697294.1:c.171+16_171+21delinsTATTTC ENSP00000513231.1:n.171+16_171+21delinsTA...
ENST00000697295.1:c.37+1819_37+1824delinsTATTTC ENSP00000513232.1:n.37+1819_37+1824delins...
ENST00000697296.1:c.171+16_171+21delinsTATTTC ENSP00000513233.1:n.171+16_171+21delinsTA...
ENST00000697297.1:n.293_298delinsTATTTC
ENST00000697298.1:c.-126+16_-126+21delinsTATTTC ENSP00000513234.1:n.-126+16_-126+21delins...
ENST00000697299.1:c.-75-1183_-75-1178delinsTATTTC ENSP00000513235.1:n.-75-1183_-75-1178deli...
ENST00000697300.1:c.-126+16_-126+21delinsTATTTC ENSP00000513236.1:n.-126+16_-126+21delins...
ENST00000697301.1:c.-126+16_-126+21delinsTATTTC ENSP00000513237.1:n.-126+16_-126+21delins...
ENST00000697302.1:c.171+16_171+21delinsTATTTC ENSP00000513238.1:n.171+16_171+21delinsTA...
ENST00000697303.1:c.171+16_171+21delinsTATTTC ENSP00000513239.1:n.171+16_171+21delinsTA...
ENST00000697304.1:c.171+16_171+21delinsTATTTC ENSP00000513240.1:n.171+16_171+21delinsTA...
ENST00000697306.1:c.171+16_171+21delinsTATTTC ENSP00000513241.1:n.171+16_171+21delinsTA...
ENST00000697307.1:c.171+16_171+21delinsTATTTC ENSP00000513242.1:n.171+16_171+21delinsTA...
ENST00000697308.1:c.171+16_171+21delinsTATTTC ENSP00000513243.1:n.171+16_171+21delinsTA...
ENST00000697309.1:c.171+16_171+21delinsTATTTC ENSP00000513244.1:n.171+16_171+21delinsTA...
ENST00000697310.1:c.171+16_171+21delinsTATTTC ENSP00000513245.1:n.171+16_171+21delinsTA...
ENST00000697311.1:c.171+16_171+21delinsTATTTC ENSP00000513246.1:n.171+16_171+21delinsTA...
ENST00000697312.1:c.171+16_171+21delinsTATTTC ENSP00000513247.1:n.171+16_171+21delinsTA...
ENST00000697313.1:n.299_304delinsTATTTC
ENST00000697314.1:n.299_304delinsTATTTC
ENST00000697315.1:c.171+16_171+21delinsTATTTC ENSP00000513248.1:n.171+16_171+21delinsTA...
ENST00000697316.1:n.292+16_292+21delinsTATTTC
ENST00000697317.1:n.281+16_281+21delinsTATTTC
ENST00000697318.1:n.283+16_283+21delinsTATTTC
ENST00000265433.8:c.171+16_171+21delinsTATTTC MANE Select ENSP00000265433.4:n.171+16_171+21delinsTA...
ENST00000265433.7:c.171+16_171+21delinsTATTTC ENSP00000265433.3:n.171+16_171+21delinsTA...
ENST00000396252.6:c.171+16_171+21delinsTATTTC ENSP00000379551.2:n.171+16_171+21delinsTA...
ENST00000409330.5:c.-76+16_-76+21delinsTATTTC ENSP00000386924.1:n.-76+16_-76+21delinsTA...
ENST00000494804.1:n.291_296delinsTATTTC
ENST00000517337.1:c.-126+16_-126+21delinsTATTTC ENSP00000429971.1:n.-126+16_-126+21delins...
ENST00000519426.5:c.171+16_171+21delinsTATTTC ENSP00000430983.1:n.171+16_171+21delinsTA...
ENST00000523444.1:c.171+16_171+21delinsTATTTC ENSP00000428252.1:n.171+16_171+21delinsTA...
NM_001024688.2:c.-126+16_-126+21delinsTATTTC NP_001019859.1:n.-126+16_-126+21delinsTAT...
NM_002485.4:c.171+16_171+21delinsTATTTC , LRG_158t1:c.171+16_171+21delinsTATTTC NP_002476.2:n.171+16_171+21delinsTATTTC
XM_011517044.1:c.147+16_147+21delinsTATTTC XP_011515346.1:n.147+16_147+21delinsTATTT...
XM_011517045.1:c.-126+16_-126+21delinsTATTTC XP_011515347.1:n.-126+16_-126+21delinsTAT...
XM_011517046.1:c.171+16_171+21delinsTATTTC XP_011515348.1:n.171+16_171+21delinsTATTT...
XR_928335.1:n.308+16_308+21delinsTATTTC
XM_017013460.1:c.-849+16_-849+21delinsTATTTC XP_016868949.1:n.-849+16_-849+21delinsTAT...
XM_017013462.2:c.-655+16_-655+21delinsTATTTC XP_016868951.1:n.-655+16_-655+21delinsTAT...
XM_024447163.1:c.-76+16_-76+21delinsTATTTC XP_024302931.1:n.-76+16_-76+21delinsTATTT...
XM_024447165.1:c.-799+16_-799+21delinsTATTTC XP_024302933.1:n.-799+16_-799+21delinsTAT...
NM_002485.5:c.171+16_171+21delinsTATTTC MANE Select NP_002476.2:n.171+16_171+21delinsTATTTC
NM_001024688.3:c.-126+16_-126+21delinsTATTTC NP_001019859.1:n.-126+16_-126+21delinsTAT...