Canonical Allele Identifier: CA1801507271
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89971193T= , CM000670.2:g.89971193T= GRCh38
NC_000008.10:g.90983421T= , CM000670.1:g.90983421T= GRCh37
NC_000008.9:g.91052597T= NCBI36
NG_008860.1:g.18479A= , LRG_158:g.18479A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1984A=
ENST00000517337.2:c.436A= ENSP00000429971.2:p.Ile146=
ENST00000523444.2:c.436A= ENSP00000428252.2:p.Ile146=
ENST00000697292.1:c.682A= ENSP00000513229.1:p.Ile228=
ENST00000697293.1:c.682A= ENSP00000513230.1:p.Ile228=
ENST00000697294.1:c.*293A= ENSP00000513231.1:n.*293A=
ENST00000697295.1:c.135A= ENSP00000513232.1:p.Leu45=
ENST00000697296.1:c.*350A= ENSP00000513233.1:n.*350A=
ENST00000697297.1:n.2467A=
ENST00000697298.1:c.436A= ENSP00000513234.1:p.Ile146=
ENST00000697299.1:c.436A= ENSP00000513235.1:p.Ile146=
ENST00000697300.1:c.*286A= ENSP00000513236.1:n.*286A=
ENST00000697301.1:c.*203A= ENSP00000513237.1:n.*203A=
ENST00000697302.1:c.*203A= ENSP00000513238.1:n.*203A=
ENST00000697303.1:c.*286A= ENSP00000513239.1:n.*286A=
ENST00000697304.1:c.585-6686A= ENSP00000513240.1:n.585-6686A=
ENST00000697306.1:c.480+9541A= ENSP00000513241.1:n.480+9541A=
ENST00000697307.1:c.682A= ENSP00000513242.1:p.Ile228=
ENST00000697308.1:c.682A= ENSP00000513243.1:p.Ile228=
ENST00000697309.1:c.682A= ENSP00000513244.1:p.Ile228=
ENST00000697310.1:c.682A= ENSP00000513245.1:p.Ile228=
ENST00000697311.1:c.682A= ENSP00000513246.1:p.Ile228=
ENST00000697312.1:c.*80A= ENSP00000513247.1:n.*80A=
ENST00000697313.1:n.2473A=
ENST00000697314.1:n.2473A=
ENST00000697315.1:c.682A= ENSP00000513248.1:p.Ile228=
ENST00000697316.1:n.803A=
ENST00000697317.1:n.792A=
ENST00000697318.1:n.794A=
ENST00000265433.8:c.682A= MANE Select ENSP00000265433.4:p.Ile228=
ENST00000265433.7:c.682A= ENSP00000265433.3:p.Ile228=
ENST00000396252.6:c.*555A= ENSP00000379551.2:n.*555A=
ENST00000409330.5:c.436A= ENSP00000386924.1:p.Ile146=
ENST00000517772.5:c.436A= ENSP00000428717.1:p.Ile146=
ENST00000519426.5:c.418A= ENSP00000430983.1:p.Ile140=
NM_001024688.2:c.436A= NP_001019859.1:p.Ile146=
NM_002485.4:c.682A= , LRG_158t1:c.682A= NP_002476.2:p.Ile228=
XM_011517044.1:c.658A= XP_011515346.1:p.Ile220=
XM_011517045.1:c.436A= XP_011515347.1:p.Ile146=
XM_011517046.1:c.682A= XP_011515348.1:p.Ile228=
XR_928335.1:n.819A=
XM_017013460.1:c.-198A= XP_016868949.1:n.-198A=
XM_017013462.2:c.-198A= XP_016868951.1:n.-198A=
XM_024447163.1:c.436A= XP_024302931.1:p.Ile146=
XM_024447164.1:c.436A= XP_024302932.1:p.Ile146=
XM_024447165.1:c.-198A= XP_024302933.1:n.-198A=
NM_002485.5:c.682A= MANE Select NP_002476.2:p.Ile228=
NM_001024688.3:c.436A= NP_001019859.1:p.Ile146=