Canonical Allele Identifier: CA371662109

Gene: NBN

Linked Data

• ClinVar Variation Id: 2855413
• ClinVar RCV Id: RCV003617507
• MyVariant Identifiers: chr8:g.90993093A>T (hg19) ; chr8:g.89980865A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89980865A>T , CM000670.2:g.89980865A>T	GRCh38
NC_000008.10:g.90993093A>T , CM000670.1:g.90993093A>T	GRCh37
NC_000008.9:g.91062269A>T	NCBI36
NG_008860.1:g.8807T>A , LRG_158:g.8807T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.1651T>A
ENST00000517337.2:c.103T>A	ENSP00000429971.2:p.Ser35Thr
ENST00000523444.2:c.103T>A	ENSP00000428252.2:p.Ser35Thr
ENST00000697292.1:c.349T>A	ENSP00000513229.1:p.Ser117Thr
ENST00000697293.1:c.349T>A	ENSP00000513230.1:p.Ser117Thr
ENST00000697294.1:c.321-13T>A	ENSP00000513231.1:n.321-13T>A
ENST00000697295.1:c.37+3660T>A	ENSP00000513232.1:n.37+3660T>A
ENST00000697296.1:c.*17T>A	ENSP00000513233.1:n.*17T>A
ENST00000697297.1:n.2134T>A
ENST00000697298.1:c.103T>A	ENSP00000513234.1:p.Ser35Thr
ENST00000697299.1:c.103T>A	ENSP00000513235.1:p.Ser35Thr
ENST00000697300.1:c.103T>A	ENSP00000513236.1:p.Ser35Thr
ENST00000697301.1:c.75-13T>A	ENSP00000513237.1:n.75-13T>A
ENST00000697302.1:c.321-13T>A	ENSP00000513238.1:n.321-13T>A
ENST00000697303.1:c.349T>A	ENSP00000513239.1:p.Ser117Thr
ENST00000697304.1:c.349T>A	ENSP00000513240.1:p.Ser117Thr
ENST00000697306.1:c.349T>A	ENSP00000513241.1:p.Ser117Thr
ENST00000697307.1:c.349T>A	ENSP00000513242.1:p.Ser117Thr
ENST00000697308.1:c.349T>A	ENSP00000513243.1:p.Ser117Thr
ENST00000697309.1:c.349T>A	ENSP00000513244.1:p.Ser117Thr
ENST00000697310.1:c.349T>A	ENSP00000513245.1:p.Ser117Thr
ENST00000697311.1:c.349T>A	ENSP00000513246.1:p.Ser117Thr
ENST00000697312.1:c.349T>A	ENSP00000513247.1:p.Ser117Thr
ENST00000697313.1:n.2140T>A
ENST00000697314.1:n.2140T>A
ENST00000697315.1:c.349T>A	ENSP00000513248.1:p.Ser117Thr
ENST00000697316.1:n.470T>A
ENST00000697317.1:n.459T>A
ENST00000697318.1:n.461T>A
ENST00000265433.8:c.349T>A MANE Select	ENSP00000265433.4:p.Ser117Thr
ENST00000265433.7:c.349T>A	ENSP00000265433.3:p.Ser117Thr
ENST00000396252.6:c.*222T>A	ENSP00000379551.2:n.*222T>A
ENST00000409330.5:c.103T>A	ENSP00000386924.1:p.Ser35Thr
ENST00000517337.1:c.103T>A	ENSP00000429971.1:p.Ser35Thr
ENST00000517772.5:c.103T>A	ENSP00000428717.1:p.Ser35Thr
ENST00000519426.5:c.320+510T>A	ENSP00000430983.1:n.320+510T>A
ENST00000523444.1:c.*194-13T>A	ENSP00000428252.1:n.*194-13T>A
NM_001024688.2:c.103T>A	NP_001019859.1:p.Ser35Thr
NM_002485.4:c.349T>A , LRG_158t1:c.349T>A	NP_002476.2:p.Ser117Thr
XM_011517044.1:c.325T>A	XP_011515346.1:p.Ser109Thr
XM_011517045.1:c.103T>A	XP_011515347.1:p.Ser35Thr
XM_011517046.1:c.349T>A	XP_011515348.1:p.Ser117Thr
XR_928335.1:n.486T>A
XM_017013460.1:c.-621T>A	XP_016868949.1:n.-621T>A
XM_017013462.2:c.-427T>A	XP_016868951.1:n.-427T>A
XM_024447163.1:c.103T>A	XP_024302931.1:p.Ser35Thr
XM_024447164.1:c.103T>A	XP_024302932.1:p.Ser35Thr
XM_024447165.1:c.-621T>A	XP_024302933.1:n.-621T>A
NM_002485.5:c.349T>A MANE Select	NP_002476.2:p.Ser117Thr
NM_001024688.3:c.103T>A	NP_001019859.1:p.Ser35Thr