Canonical Allele Identifier: CA371655637

Gene: NBN

Linked Data

• dbSNP Id: rs2129701484
• gnomAD v4: 8-89953549-C-T
• MyVariant Identifiers: chr8:g.90965777C>T (hg19) ; chr8:g.89953549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953549C>T , CM000670.2:g.89953549C>T	GRCh38
NC_000008.10:g.90965777C>T , CM000670.1:g.90965777C>T	GRCh37
NC_000008.9:g.91034953C>T	NCBI36
NG_008860.1:g.36123G>A , LRG_158:g.36123G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2842G>A
ENST00000517337.2:c.1294G>A	ENSP00000429971.2:p.Val432Met
ENST00000523444.2:c.1294G>A	ENSP00000428252.2:p.Val432Met
ENST00000697292.1:c.1540G>A	ENSP00000513229.1:p.Val514Met
ENST00000697293.1:c.1540G>A	ENSP00000513230.1:p.Val514Met
ENST00000697294.1:c.*1151G>A	ENSP00000513231.1:n.*1151G>A
ENST00000697295.1:c.*849G>A	ENSP00000513232.1:n.*849G>A
ENST00000697296.1:c.*1208G>A	ENSP00000513233.1:n.*1208G>A
ENST00000697297.1:n.3325G>A
ENST00000697298.1:c.1294G>A	ENSP00000513234.1:p.Val432Met
ENST00000697299.1:c.1294G>A	ENSP00000513235.1:p.Val432Met
ENST00000697300.1:c.*1144G>A	ENSP00000513236.1:n.*1144G>A
ENST00000697301.1:c.*1061G>A	ENSP00000513237.1:n.*1061G>A
ENST00000697302.1:c.*1061G>A	ENSP00000513238.1:n.*1061G>A
ENST00000697303.1:c.*1144G>A	ENSP00000513239.1:n.*1144G>A
ENST00000697304.1:c.1228G>A	ENSP00000513240.1:p.Val410Met
ENST00000697306.1:c.*540G>A	ENSP00000513241.1:n.*540G>A
ENST00000697307.1:c.1540G>A	ENSP00000513242.1:p.Val514Met
ENST00000697308.1:c.1540G>A	ENSP00000513243.1:p.Val514Met
ENST00000697309.1:c.1540G>A	ENSP00000513244.1:p.Val514Met
ENST00000697310.1:c.1540G>A	ENSP00000513245.1:p.Val514Met
ENST00000697311.1:c.1540G>A	ENSP00000513246.1:p.Val514Met
ENST00000697312.1:c.*938G>A	ENSP00000513247.1:n.*938G>A
ENST00000697313.1:n.2687+16815G>A
ENST00000697314.1:n.3331G>A
ENST00000697315.1:c.1540G>A	ENSP00000513248.1:p.Val514Met
ENST00000697316.1:n.1661G>A
ENST00000697317.1:n.1650G>A
ENST00000697318.1:n.1652G>A
ENST00000265433.8:c.1540G>A MANE Select	ENSP00000265433.4:p.Val514Met
ENST00000265433.7:c.1540G>A	ENSP00000265433.3:p.Val514Met
ENST00000396252.6:c.*1413G>A	ENSP00000379551.2:n.*1413G>A
ENST00000409330.5:c.1294G>A	ENSP00000386924.1:p.Val432Met
NM_001024688.2:c.1294G>A	NP_001019859.1:p.Val432Met
NM_002485.4:c.1540G>A , LRG_158t1:c.1540G>A	NP_002476.2:p.Val514Met
XM_011517044.1:c.1516G>A	XP_011515346.1:p.Val506Met
XM_011517045.1:c.1294G>A	XP_011515347.1:p.Val432Met
XR_928335.1:n.1679G>A
XM_017013460.1:c.661G>A	XP_016868949.1:p.Val221Met
XM_017013462.2:c.661G>A	XP_016868951.1:p.Val221Met
XM_024447163.1:c.1294G>A	XP_024302931.1:p.Val432Met
XM_024447164.1:c.1294G>A	XP_024302932.1:p.Val432Met
XM_024447165.1:c.661G>A	XP_024302933.1:p.Val221Met
NM_002485.5:c.1540G>A MANE Select	NP_002476.2:p.Val514Met
NM_001024688.3:c.1294G>A	NP_001019859.1:p.Val432Met