Canonical Allele Identifier: CA371659269

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90983487C>G (hg19) ; chr8:g.89971259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89971259C>G , CM000670.2:g.89971259C>G	GRCh38
NC_000008.10:g.90983487C>G , CM000670.1:g.90983487C>G	GRCh37
NC_000008.9:g.91052663C>G	NCBI36
NG_008860.1:g.18413G>C , LRG_158:g.18413G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.1918G>C
ENST00000517337.2:c.370G>C	ENSP00000429971.2:p.Gly124Arg
ENST00000523444.2:c.370G>C	ENSP00000428252.2:p.Gly124Arg
ENST00000697292.1:c.616G>C	ENSP00000513229.1:p.Gly206Arg
ENST00000697293.1:c.616G>C	ENSP00000513230.1:p.Gly206Arg
ENST00000697294.1:c.*227G>C	ENSP00000513231.1:n.*227G>C
ENST00000697295.1:c.69G>C	ENSP00000513232.1:p.Leu23Phe
ENST00000697296.1:c.*284G>C	ENSP00000513233.1:n.*284G>C
ENST00000697297.1:n.2401G>C
ENST00000697298.1:c.370G>C	ENSP00000513234.1:p.Gly124Arg
ENST00000697299.1:c.370G>C	ENSP00000513235.1:p.Gly124Arg
ENST00000697300.1:c.*220G>C	ENSP00000513236.1:n.*220G>C
ENST00000697301.1:c.*137G>C	ENSP00000513237.1:n.*137G>C
ENST00000697302.1:c.*137G>C	ENSP00000513238.1:n.*137G>C
ENST00000697303.1:c.*220G>C	ENSP00000513239.1:n.*220G>C
ENST00000697304.1:c.585-6752G>C	ENSP00000513240.1:n.585-6752G>C
ENST00000697306.1:c.480+9475G>C	ENSP00000513241.1:n.480+9475G>C
ENST00000697307.1:c.616G>C	ENSP00000513242.1:p.Gly206Arg
ENST00000697308.1:c.616G>C	ENSP00000513243.1:p.Gly206Arg
ENST00000697309.1:c.616G>C	ENSP00000513244.1:p.Gly206Arg
ENST00000697310.1:c.616G>C	ENSP00000513245.1:p.Gly206Arg
ENST00000697311.1:c.616G>C	ENSP00000513246.1:p.Gly206Arg
ENST00000697312.1:c.*14G>C	ENSP00000513247.1:n.*14G>C
ENST00000697313.1:n.2407G>C
ENST00000697314.1:n.2407G>C
ENST00000697315.1:c.616G>C	ENSP00000513248.1:p.Gly206Arg
ENST00000697316.1:n.737G>C
ENST00000697317.1:n.726G>C
ENST00000697318.1:n.728G>C
ENST00000265433.8:c.616G>C MANE Select	ENSP00000265433.4:p.Gly206Arg
ENST00000265433.7:c.616G>C	ENSP00000265433.3:p.Gly206Arg
ENST00000396252.6:c.*489G>C	ENSP00000379551.2:n.*489G>C
ENST00000409330.5:c.370G>C	ENSP00000386924.1:p.Gly124Arg
ENST00000517772.5:c.370G>C	ENSP00000428717.1:p.Gly124Arg
ENST00000519426.5:c.352G>C	ENSP00000430983.1:p.Gly118Arg
NM_001024688.2:c.370G>C	NP_001019859.1:p.Gly124Arg
NM_002485.4:c.616G>C , LRG_158t1:c.616G>C	NP_002476.2:p.Gly206Arg
XM_011517044.1:c.592G>C	XP_011515346.1:p.Gly198Arg
XM_011517045.1:c.370G>C	XP_011515347.1:p.Gly124Arg
XM_011517046.1:c.616G>C	XP_011515348.1:p.Gly206Arg
XR_928335.1:n.753G>C
XM_017013460.1:c.-264G>C	XP_016868949.1:n.-264G>C
XM_017013462.2:c.-264G>C	XP_016868951.1:n.-264G>C
XM_024447163.1:c.370G>C	XP_024302931.1:p.Gly124Arg
XM_024447164.1:c.370G>C	XP_024302932.1:p.Gly124Arg
XM_024447165.1:c.-264G>C	XP_024302933.1:n.-264G>C
NM_002485.5:c.616G>C MANE Select	NP_002476.2:p.Gly206Arg
NM_001024688.3:c.370G>C	NP_001019859.1:p.Gly124Arg