Canonical Allele Identifier: CA1801507504
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89971235C= , CM000670.2:g.89971235C= GRCh38
NC_000008.10:g.90983463C= , CM000670.1:g.90983463C= GRCh37
NC_000008.9:g.91052639C= NCBI36
NG_008860.1:g.18437G= , LRG_158:g.18437G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1942G=
ENST00000517337.2:c.394G= ENSP00000429971.2:p.Gly132=
ENST00000523444.2:c.394G= ENSP00000428252.2:p.Gly132=
ENST00000697292.1:c.640G= ENSP00000513229.1:p.Gly214=
ENST00000697293.1:c.640G= ENSP00000513230.1:p.Gly214=
ENST00000697294.1:c.*251G= ENSP00000513231.1:n.*251G=
ENST00000697295.1:c.93G= ENSP00000513232.1:p.Gln31=
ENST00000697296.1:c.*308G= ENSP00000513233.1:n.*308G=
ENST00000697297.1:n.2425G=
ENST00000697298.1:c.394G= ENSP00000513234.1:p.Gly132=
ENST00000697299.1:c.394G= ENSP00000513235.1:p.Gly132=
ENST00000697300.1:c.*244G= ENSP00000513236.1:n.*244G=
ENST00000697301.1:c.*161G= ENSP00000513237.1:n.*161G=
ENST00000697302.1:c.*161G= ENSP00000513238.1:n.*161G=
ENST00000697303.1:c.*244G= ENSP00000513239.1:n.*244G=
ENST00000697304.1:c.585-6728G= ENSP00000513240.1:n.585-6728G=
ENST00000697306.1:c.480+9499G= ENSP00000513241.1:n.480+9499G=
ENST00000697307.1:c.640G= ENSP00000513242.1:p.Gly214=
ENST00000697308.1:c.640G= ENSP00000513243.1:p.Gly214=
ENST00000697309.1:c.640G= ENSP00000513244.1:p.Gly214=
ENST00000697310.1:c.640G= ENSP00000513245.1:p.Gly214=
ENST00000697311.1:c.640G= ENSP00000513246.1:p.Gly214=
ENST00000697312.1:c.*38G= ENSP00000513247.1:n.*38G=
ENST00000697313.1:n.2431G=
ENST00000697314.1:n.2431G=
ENST00000697315.1:c.640G= ENSP00000513248.1:p.Gly214=
ENST00000697316.1:n.761G=
ENST00000697317.1:n.750G=
ENST00000697318.1:n.752G=
ENST00000265433.8:c.640G= MANE Select ENSP00000265433.4:p.Gly214=
ENST00000265433.7:c.640G= ENSP00000265433.3:p.Gly214=
ENST00000396252.6:c.*513G= ENSP00000379551.2:n.*513G=
ENST00000409330.5:c.394G= ENSP00000386924.1:p.Gly132=
ENST00000517772.5:c.394G= ENSP00000428717.1:p.Gly132=
ENST00000519426.5:c.376G= ENSP00000430983.1:p.Gly126=
NM_001024688.2:c.394G= NP_001019859.1:p.Gly132=
NM_002485.4:c.640G= , LRG_158t1:c.640G= NP_002476.2:p.Gly214=
XM_011517044.1:c.616G= XP_011515346.1:p.Gly206=
XM_011517045.1:c.394G= XP_011515347.1:p.Gly132=
XM_011517046.1:c.640G= XP_011515348.1:p.Gly214=
XR_928335.1:n.777G=
XM_017013460.1:c.-240G= XP_016868949.1:n.-240G=
XM_017013462.2:c.-240G= XP_016868951.1:n.-240G=
XM_024447163.1:c.394G= XP_024302931.1:p.Gly132=
XM_024447164.1:c.394G= XP_024302932.1:p.Gly132=
XM_024447165.1:c.-240G= XP_024302933.1:n.-240G=
NM_002485.5:c.640G= MANE Select NP_002476.2:p.Gly214=
NM_001024688.3:c.394G= NP_001019859.1:p.Gly132=