Canonical Allele Identifier: CA1801422837

Gene: NBN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953388G= , CM000670.2:g.89953388G=	GRCh38
NC_000008.10:g.90965616G= , CM000670.1:g.90965616G=	GRCh37
NC_000008.9:g.91034792G=	NCBI36
NG_008860.1:g.36284C= , LRG_158:g.36284C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3003C=
ENST00000517337.2:c.1455C=	ENSP00000429971.2:p.Phe485=
ENST00000523444.2:c.1455C=	ENSP00000428252.2:p.Phe485=
ENST00000697292.1:c.1701C=	ENSP00000513229.1:p.Phe567=
ENST00000697293.1:c.1701C=	ENSP00000513230.1:p.Phe567=
ENST00000697294.1:c.*1312C=	ENSP00000513231.1:n.*1312C=
ENST00000697295.1:c.*1010C=	ENSP00000513232.1:n.*1010C=
ENST00000697296.1:c.*1369C=	ENSP00000513233.1:n.*1369C=
ENST00000697297.1:n.3486C=
ENST00000697298.1:c.1455C=	ENSP00000513234.1:p.Phe485=
ENST00000697299.1:c.1455C=	ENSP00000513235.1:p.Phe485=
ENST00000697300.1:c.*1305C=	ENSP00000513236.1:n.*1305C=
ENST00000697301.1:c.*1222C=	ENSP00000513237.1:n.*1222C=
ENST00000697302.1:c.*1222C=	ENSP00000513238.1:n.*1222C=
ENST00000697303.1:c.*1305C=	ENSP00000513239.1:n.*1305C=
ENST00000697304.1:c.1389C=	ENSP00000513240.1:p.Phe463=
ENST00000697306.1:c.*701C=	ENSP00000513241.1:n.*701C=
ENST00000697307.1:c.1701C=	ENSP00000513242.1:p.Phe567=
ENST00000697308.1:c.1701C=	ENSP00000513243.1:p.Phe567=
ENST00000697309.1:c.1701C=	ENSP00000513244.1:p.Phe567=
ENST00000697310.1:c.1701C=	ENSP00000513245.1:p.Phe567=
ENST00000697311.1:c.1701C=	ENSP00000513246.1:p.Phe567=
ENST00000697312.1:c.*1099C=	ENSP00000513247.1:n.*1099C=
ENST00000697313.1:n.2687+16976C=
ENST00000697314.1:n.3492C=
ENST00000697315.1:c.1701C=	ENSP00000513248.1:p.Phe567=
ENST00000697316.1:n.1822C=
ENST00000697317.1:n.1811C=
ENST00000697318.1:n.1813C=
ENST00000265433.8:c.1701C= MANE Select	ENSP00000265433.4:p.Phe567=
ENST00000265433.7:c.1701C=	ENSP00000265433.3:p.Phe567=
ENST00000396252.6:c.*1574C=	ENSP00000379551.2:n.*1574C=
ENST00000409330.5:c.1455C=	ENSP00000386924.1:p.Phe485=
NM_001024688.2:c.1455C=	NP_001019859.1:p.Phe485=
NM_002485.4:c.1701C= , LRG_158t1:c.1701C=	NP_002476.2:p.Phe567=
XM_011517044.1:c.1677C=	XP_011515346.1:p.Phe559=
XM_011517045.1:c.1455C=	XP_011515347.1:p.Phe485=
XR_928335.1:n.1840C=
XM_017013460.1:c.822C=	XP_016868949.1:p.Phe274=
XM_017013462.2:c.822C=	XP_016868951.1:p.Phe274=
XM_024447163.1:c.1455C=	XP_024302931.1:p.Phe485=
XM_024447164.1:c.1455C=	XP_024302932.1:p.Phe485=
XM_024447165.1:c.822C=	XP_024302933.1:p.Phe274=
NM_002485.5:c.1701C= MANE Select	NP_002476.2:p.Phe567=
NM_001024688.3:c.1455C=	NP_001019859.1:p.Phe485=