Canonical Allele Identifier: CA1801507724
Gene: NBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89971283G= , CM000670.2:g.89971283G= GRCh38
NC_000008.10:g.90983511G= , CM000670.1:g.90983511G= GRCh37
NC_000008.9:g.91052687G= NCBI36
NG_008860.1:g.18389C= , LRG_158:g.18389C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1894C=
ENST00000517337.2:c.346C= ENSP00000429971.2:p.Pro116=
ENST00000523444.2:c.346C= ENSP00000428252.2:p.Pro116=
ENST00000697292.1:c.592C= ENSP00000513229.1:p.Pro198=
ENST00000697293.1:c.592C= ENSP00000513230.1:p.Pro198=
ENST00000697294.1:c.*203C= ENSP00000513231.1:n.*203C=
ENST00000697295.1:c.45C= ENSP00000513232.1:p.Thr15=
ENST00000697296.1:c.*260C= ENSP00000513233.1:n.*260C=
ENST00000697297.1:n.2377C=
ENST00000697298.1:c.346C= ENSP00000513234.1:p.Pro116=
ENST00000697299.1:c.346C= ENSP00000513235.1:p.Pro116=
ENST00000697300.1:c.*196C= ENSP00000513236.1:n.*196C=
ENST00000697301.1:c.*113C= ENSP00000513237.1:n.*113C=
ENST00000697302.1:c.*113C= ENSP00000513238.1:n.*113C=
ENST00000697303.1:c.*196C= ENSP00000513239.1:n.*196C=
ENST00000697304.1:c.585-6776C= ENSP00000513240.1:n.585-6776C=
ENST00000697306.1:c.480+9451C= ENSP00000513241.1:n.480+9451C=
ENST00000697307.1:c.592C= ENSP00000513242.1:p.Pro198=
ENST00000697308.1:c.592C= ENSP00000513243.1:p.Pro198=
ENST00000697309.1:c.592C= ENSP00000513244.1:p.Pro198=
ENST00000697310.1:c.592C= ENSP00000513245.1:p.Pro198=
ENST00000697311.1:c.592C= ENSP00000513246.1:p.Pro198=
ENST00000697312.1:c.488C= ENSP00000513247.1:p.Pro163=
ENST00000697313.1:n.2383C=
ENST00000697314.1:n.2383C=
ENST00000697315.1:c.592C= ENSP00000513248.1:p.Pro198=
ENST00000697316.1:n.713C=
ENST00000697317.1:n.702C=
ENST00000697318.1:n.704C=
ENST00000265433.8:c.592C= MANE Select ENSP00000265433.4:p.Pro198=
ENST00000265433.7:c.592C= ENSP00000265433.3:p.Pro198=
ENST00000396252.6:c.*465C= ENSP00000379551.2:n.*465C=
ENST00000409330.5:c.346C= ENSP00000386924.1:p.Pro116=
ENST00000517772.5:c.346C= ENSP00000428717.1:p.Pro116=
ENST00000519426.5:c.328C= ENSP00000430983.1:p.Pro110=
NM_001024688.2:c.346C= NP_001019859.1:p.Pro116=
NM_002485.4:c.592C= , LRG_158t1:c.592C= NP_002476.2:p.Pro198=
XM_011517044.1:c.568C= XP_011515346.1:p.Pro190=
XM_011517045.1:c.346C= XP_011515347.1:p.Pro116=
XM_011517046.1:c.592C= XP_011515348.1:p.Pro198=
XR_928335.1:n.729C=
XM_017013460.1:c.-288C= XP_016868949.1:n.-288C=
XM_017013462.2:c.-288C= XP_016868951.1:n.-288C=
XM_024447163.1:c.346C= XP_024302931.1:p.Pro116=
XM_024447164.1:c.346C= XP_024302932.1:p.Pro116=
XM_024447165.1:c.-288C= XP_024302933.1:n.-288C=
NM_002485.5:c.592C= MANE Select NP_002476.2:p.Pro198=
NM_001024688.3:c.346C= NP_001019859.1:p.Pro116=