Canonical Allele Identifier: CA371655743

Gene: NBN

Linked Data

• ClinVar Variation Id: 2702798
• ClinVar RCV Id: RCV003508020
• MyVariant Identifiers: chr8:g.90965824G>T (hg19) ; chr8:g.89953596G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953596G>T , CM000670.2:g.89953596G>T	GRCh38
NC_000008.10:g.90965824G>T , CM000670.1:g.90965824G>T	GRCh37
NC_000008.9:g.91035000G>T	NCBI36
NG_008860.1:g.36076C>A , LRG_158:g.36076C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2795C>A
ENST00000517337.2:c.1247C>A	ENSP00000429971.2:p.Pro416His
ENST00000523444.2:c.1247C>A	ENSP00000428252.2:p.Pro416His
ENST00000697292.1:c.1493C>A	ENSP00000513229.1:p.Pro498His
ENST00000697293.1:c.1493C>A	ENSP00000513230.1:p.Pro498His
ENST00000697294.1:c.*1104C>A	ENSP00000513231.1:n.*1104C>A
ENST00000697295.1:c.*802C>A	ENSP00000513232.1:n.*802C>A
ENST00000697296.1:c.*1161C>A	ENSP00000513233.1:n.*1161C>A
ENST00000697297.1:n.3278C>A
ENST00000697298.1:c.1247C>A	ENSP00000513234.1:p.Pro416His
ENST00000697299.1:c.1247C>A	ENSP00000513235.1:p.Pro416His
ENST00000697300.1:c.*1097C>A	ENSP00000513236.1:n.*1097C>A
ENST00000697301.1:c.*1014C>A	ENSP00000513237.1:n.*1014C>A
ENST00000697302.1:c.*1014C>A	ENSP00000513238.1:n.*1014C>A
ENST00000697303.1:c.*1097C>A	ENSP00000513239.1:n.*1097C>A
ENST00000697304.1:c.1181C>A	ENSP00000513240.1:p.Pro394His
ENST00000697306.1:c.*493C>A	ENSP00000513241.1:n.*493C>A
ENST00000697307.1:c.1493C>A	ENSP00000513242.1:p.Pro498His
ENST00000697308.1:c.1493C>A	ENSP00000513243.1:p.Pro498His
ENST00000697309.1:c.1493C>A	ENSP00000513244.1:p.Pro498His
ENST00000697310.1:c.1493C>A	ENSP00000513245.1:p.Pro498His
ENST00000697311.1:c.1493C>A	ENSP00000513246.1:p.Pro498His
ENST00000697312.1:c.*891C>A	ENSP00000513247.1:n.*891C>A
ENST00000697313.1:n.2687+16768C>A
ENST00000697314.1:n.3284C>A
ENST00000697315.1:c.1493C>A	ENSP00000513248.1:p.Pro498His
ENST00000697316.1:n.1614C>A
ENST00000697317.1:n.1603C>A
ENST00000697318.1:n.1605C>A
ENST00000265433.8:c.1493C>A MANE Select	ENSP00000265433.4:p.Pro498His
ENST00000265433.7:c.1493C>A	ENSP00000265433.3:p.Pro498His
ENST00000396252.6:c.*1366C>A	ENSP00000379551.2:n.*1366C>A
ENST00000409330.5:c.1247C>A	ENSP00000386924.1:p.Pro416His
NM_001024688.2:c.1247C>A	NP_001019859.1:p.Pro416His
NM_002485.4:c.1493C>A , LRG_158t1:c.1493C>A	NP_002476.2:p.Pro498His
XM_011517044.1:c.1469C>A	XP_011515346.1:p.Pro490His
XM_011517045.1:c.1247C>A	XP_011515347.1:p.Pro416His
XR_928335.1:n.1632C>A
XM_017013460.1:c.614C>A	XP_016868949.1:p.Pro205His
XM_017013462.2:c.614C>A	XP_016868951.1:p.Pro205His
XM_024447163.1:c.1247C>A	XP_024302931.1:p.Pro416His
XM_024447164.1:c.1247C>A	XP_024302932.1:p.Pro416His
XM_024447165.1:c.614C>A	XP_024302933.1:p.Pro205His
NM_002485.5:c.1493C>A MANE Select	NP_002476.2:p.Pro498His
NM_001024688.3:c.1247C>A	NP_001019859.1:p.Pro416His