Canonical Allele Identifier: CA371655713

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90965810T>G (hg19) ; chr8:g.89953582T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953582T>G , CM000670.2:g.89953582T>G	GRCh38
NC_000008.10:g.90965810T>G , CM000670.1:g.90965810T>G	GRCh37
NC_000008.9:g.91034986T>G	NCBI36
NG_008860.1:g.36090A>C , LRG_158:g.36090A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2809A>C
ENST00000517337.2:c.1261A>C	ENSP00000429971.2:p.Asn421His
ENST00000523444.2:c.1261A>C	ENSP00000428252.2:p.Asn421His
ENST00000697292.1:c.1507A>C	ENSP00000513229.1:p.Asn503His
ENST00000697293.1:c.1507A>C	ENSP00000513230.1:p.Asn503His
ENST00000697294.1:c.*1118A>C	ENSP00000513231.1:n.*1118A>C
ENST00000697295.1:c.*816A>C	ENSP00000513232.1:n.*816A>C
ENST00000697296.1:c.*1175A>C	ENSP00000513233.1:n.*1175A>C
ENST00000697297.1:n.3292A>C
ENST00000697298.1:c.1261A>C	ENSP00000513234.1:p.Asn421His
ENST00000697299.1:c.1261A>C	ENSP00000513235.1:p.Asn421His
ENST00000697300.1:c.*1111A>C	ENSP00000513236.1:n.*1111A>C
ENST00000697301.1:c.*1028A>C	ENSP00000513237.1:n.*1028A>C
ENST00000697302.1:c.*1028A>C	ENSP00000513238.1:n.*1028A>C
ENST00000697303.1:c.*1111A>C	ENSP00000513239.1:n.*1111A>C
ENST00000697304.1:c.1195A>C	ENSP00000513240.1:p.Asn399His
ENST00000697306.1:c.*507A>C	ENSP00000513241.1:n.*507A>C
ENST00000697307.1:c.1507A>C	ENSP00000513242.1:p.Asn503His
ENST00000697308.1:c.1507A>C	ENSP00000513243.1:p.Asn503His
ENST00000697309.1:c.1507A>C	ENSP00000513244.1:p.Asn503His
ENST00000697310.1:c.1507A>C	ENSP00000513245.1:p.Asn503His
ENST00000697311.1:c.1507A>C	ENSP00000513246.1:p.Asn503His
ENST00000697312.1:c.*905A>C	ENSP00000513247.1:n.*905A>C
ENST00000697313.1:n.2687+16782A>C
ENST00000697314.1:n.3298A>C
ENST00000697315.1:c.1507A>C	ENSP00000513248.1:p.Asn503His
ENST00000697316.1:n.1628A>C
ENST00000697317.1:n.1617A>C
ENST00000697318.1:n.1619A>C
ENST00000265433.8:c.1507A>C MANE Select	ENSP00000265433.4:p.Asn503His
ENST00000265433.7:c.1507A>C	ENSP00000265433.3:p.Asn503His
ENST00000396252.6:c.*1380A>C	ENSP00000379551.2:n.*1380A>C
ENST00000409330.5:c.1261A>C	ENSP00000386924.1:p.Asn421His
NM_001024688.2:c.1261A>C	NP_001019859.1:p.Asn421His
NM_002485.4:c.1507A>C , LRG_158t1:c.1507A>C	NP_002476.2:p.Asn503His
XM_011517044.1:c.1483A>C	XP_011515346.1:p.Asn495His
XM_011517045.1:c.1261A>C	XP_011515347.1:p.Asn421His
XR_928335.1:n.1646A>C
XM_017013460.1:c.628A>C	XP_016868949.1:p.Asn210His
XM_017013462.2:c.628A>C	XP_016868951.1:p.Asn210His
XM_024447163.1:c.1261A>C	XP_024302931.1:p.Asn421His
XM_024447164.1:c.1261A>C	XP_024302932.1:p.Asn421His
XM_024447165.1:c.628A>C	XP_024302933.1:p.Asn210His
NM_002485.5:c.1507A>C MANE Select	NP_002476.2:p.Asn503His
NM_001024688.3:c.1261A>C	NP_001019859.1:p.Asn421His