Canonical Allele Identifier: CA1801470049
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89982789A= , CM000670.2:g.89982789A= GRCh38
NC_000008.10:g.90995017A= , CM000670.1:g.90995017A= GRCh37
NC_000008.9:g.91064193A= NCBI36
NG_008860.1:g.6883T= , LRG_158:g.6883T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.208T=
ENST00000517337.2:c.-193T= ENSP00000429971.2:n.-193T=
ENST00000523444.2:c.-193T= ENSP00000428252.2:n.-193T=
ENST00000697292.1:c.104T= ENSP00000513229.1:p.Ile35=
ENST00000697293.1:c.104T= ENSP00000513230.1:p.Ile35=
ENST00000697294.1:c.104T= ENSP00000513231.1:p.Ile35=
ENST00000697295.1:c.37+1736T= ENSP00000513232.1:n.37+1736T=
ENST00000697296.1:c.104T= ENSP00000513233.1:p.Ile35=
ENST00000697297.1:n.210T=
ENST00000697298.1:c.-193T= ENSP00000513234.1:n.-193T=
ENST00000697299.1:c.-75-1266T= ENSP00000513235.1:n.-75-1266T=
ENST00000697300.1:c.-193T= ENSP00000513236.1:n.-193T=
ENST00000697301.1:c.-193T= ENSP00000513237.1:n.-193T=
ENST00000697302.1:c.104T= ENSP00000513238.1:p.Ile35=
ENST00000697303.1:c.104T= ENSP00000513239.1:p.Ile35=
ENST00000697304.1:c.104T= ENSP00000513240.1:p.Ile35=
ENST00000697306.1:c.104T= ENSP00000513241.1:p.Ile35=
ENST00000697307.1:c.104T= ENSP00000513242.1:p.Ile35=
ENST00000697308.1:c.104T= ENSP00000513243.1:p.Ile35=
ENST00000697309.1:c.104T= ENSP00000513244.1:p.Ile35=
ENST00000697310.1:c.104T= ENSP00000513245.1:p.Ile35=
ENST00000697311.1:c.104T= ENSP00000513246.1:p.Ile35=
ENST00000697312.1:c.104T= ENSP00000513247.1:p.Ile35=
ENST00000697313.1:n.216T=
ENST00000697314.1:n.216T=
ENST00000697315.1:c.104T= ENSP00000513248.1:p.Ile35=
ENST00000697316.1:n.225T=
ENST00000697317.1:n.214T=
ENST00000697318.1:n.216T=
ENST00000265433.8:c.104T= MANE Select ENSP00000265433.4:p.Ile35=
ENST00000265433.7:c.104T= ENSP00000265433.3:p.Ile35=
ENST00000396252.6:c.104T= ENSP00000379551.2:p.Ile35=
ENST00000409330.5:c.-143T= ENSP00000386924.1:n.-143T=
ENST00000494804.1:n.208T=
ENST00000517337.1:c.-193T= ENSP00000429971.1:n.-193T=
ENST00000519426.5:c.104T= ENSP00000430983.1:p.Ile35=
ENST00000523444.1:c.104T= ENSP00000428252.1:p.Ile35=
NM_001024688.2:c.-193T= NP_001019859.1:n.-193T=
NM_002485.4:c.104T= , LRG_158t1:c.104T= NP_002476.2:p.Ile35=
XM_011517044.1:c.80T= XP_011515346.1:p.Ile27=
XM_011517045.1:c.-193T= XP_011515347.1:n.-193T=
XM_011517046.1:c.104T= XP_011515348.1:p.Ile35=
XR_928335.1:n.241T=
XM_017013460.1:c.-916T= XP_016868949.1:n.-916T=
XM_017013462.2:c.-722T= XP_016868951.1:n.-722T=
XM_024447163.1:c.-143T= XP_024302931.1:n.-143T=
XM_024447165.1:c.-866T= XP_024302933.1:n.-866T=
NM_002485.5:c.104T= MANE Select NP_002476.2:p.Ile35=
NM_001024688.3:c.-193T= NP_001019859.1:n.-193T=