Canonical Allele Identifier: CA1801505181

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970374T= , CM000670.2:g.89970374T=	GRCh38
NC_000008.10:g.90982602T= , CM000670.1:g.90982602T=	GRCh37
NC_000008.9:g.91051778T=	NCBI36
NG_008860.1:g.19298A= , LRG_158:g.19298A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2188A=
ENST00000517337.2:c.640A=	ENSP00000429971.2:p.Met214=
ENST00000523444.2:c.640A=	ENSP00000428252.2:p.Met214=
ENST00000697292.1:c.886A=	ENSP00000513229.1:p.Met296=
ENST00000697293.1:c.886A=	ENSP00000513230.1:p.Met296=
ENST00000697294.1:c.*497A=	ENSP00000513231.1:n.*497A=
ENST00000697295.1:c.*195A=	ENSP00000513232.1:n.*195A=
ENST00000697296.1:c.*554A=	ENSP00000513233.1:n.*554A=
ENST00000697297.1:n.2671A=
ENST00000697298.1:c.640A=	ENSP00000513234.1:p.Met214=
ENST00000697299.1:c.640A=	ENSP00000513235.1:p.Met214=
ENST00000697300.1:c.*490A=	ENSP00000513236.1:n.*490A=
ENST00000697301.1:c.*407A=	ENSP00000513237.1:n.*407A=
ENST00000697302.1:c.*407A=	ENSP00000513238.1:n.*407A=
ENST00000697303.1:c.*490A=	ENSP00000513239.1:n.*490A=
ENST00000697304.1:c.585-5867A=	ENSP00000513240.1:n.585-5867A=
ENST00000697306.1:c.480+10360A=	ENSP00000513241.1:n.480+10360A=
ENST00000697307.1:c.886A=	ENSP00000513242.1:p.Met296=
ENST00000697308.1:c.886A=	ENSP00000513243.1:p.Met296=
ENST00000697309.1:c.886A=	ENSP00000513244.1:p.Met296=
ENST00000697310.1:c.886A=	ENSP00000513245.1:p.Met296=
ENST00000697311.1:c.886A=	ENSP00000513246.1:p.Met296=
ENST00000697312.1:c.*284A=	ENSP00000513247.1:n.*284A=
ENST00000697313.1:n.2677A=
ENST00000697314.1:n.2677A=
ENST00000697315.1:c.886A=	ENSP00000513248.1:p.Met296=
ENST00000697316.1:n.1007A=
ENST00000697317.1:n.996A=
ENST00000697318.1:n.998A=
ENST00000265433.8:c.886A= MANE Select	ENSP00000265433.4:p.Met296=
ENST00000265433.7:c.886A=	ENSP00000265433.3:p.Met296=
ENST00000396252.6:c.*759A=	ENSP00000379551.2:n.*759A=
ENST00000409330.5:c.640A=	ENSP00000386924.1:p.Met214=
NM_001024688.2:c.640A=	NP_001019859.1:p.Met214=
NM_002485.4:c.886A= , LRG_158t1:c.886A=	NP_002476.2:p.Met296=
XM_011517044.1:c.862A=	XP_011515346.1:p.Met288=
XM_011517045.1:c.640A=	XP_011515347.1:p.Met214=
XM_011517046.1:c.886A=	XP_011515348.1:p.Met296=
XR_928335.1:n.1023A=
XM_017013460.1:c.7A=	XP_016868949.1:p.Met3=
XM_017013462.2:c.7A=	XP_016868951.1:p.Met3=
XM_024447163.1:c.640A=	XP_024302931.1:p.Met214=
XM_024447164.1:c.640A=	XP_024302932.1:p.Met214=
XM_024447165.1:c.7A=	XP_024302933.1:p.Met3=
NM_002485.5:c.886A= MANE Select	NP_002476.2:p.Met296=
NM_001024688.3:c.640A=	NP_001019859.1:p.Met214=