Canonical Allele Identifier: CA371676770

Gene: NBN

Linked Data

• ClinVar Variation Id: 480032
• ClinVar RCV Id: RCV000565372 ; RCV001571743 ; RCV001071353
• dbSNP Id: rs1064796613
• MyVariant Identifiers: chr8:g.90958505C>A (hg19) ; chr8:g.89946277C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946277C>A , CM000670.2:g.89946277C>A	GRCh38
NC_000008.10:g.90958505C>A , CM000670.1:g.90958505C>A	GRCh37
NC_000008.9:g.91027681C>A	NCBI36
NG_008860.1:g.43395G>T , LRG_158:g.43395G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3235G>T
ENST00000517337.2:c.1687G>T	ENSP00000429971.2:p.Asp563Tyr
ENST00000523444.2:c.1687G>T	ENSP00000428252.2:p.Asp563Tyr
ENST00000697292.1:c.1933G>T	ENSP00000513229.1:p.Asp645Tyr
ENST00000697293.1:c.1933G>T	ENSP00000513230.1:p.Asp645Tyr
ENST00000697294.1:c.*1544G>T	ENSP00000513231.1:n.*1544G>T
ENST00000697295.1:c.*1242G>T	ENSP00000513232.1:n.*1242G>T
ENST00000697296.1:c.*1601G>T	ENSP00000513233.1:n.*1601G>T
ENST00000697297.1:n.3718G>T
ENST00000697298.1:c.1687G>T	ENSP00000513234.1:p.Asp563Tyr
ENST00000697299.1:c.1687G>T	ENSP00000513235.1:p.Asp563Tyr
ENST00000697300.1:c.*1537G>T	ENSP00000513236.1:n.*1537G>T
ENST00000697301.1:c.*1454G>T	ENSP00000513237.1:n.*1454G>T
ENST00000697302.1:c.*1454G>T	ENSP00000513238.1:n.*1454G>T
ENST00000697303.1:c.*1537G>T	ENSP00000513239.1:n.*1537G>T
ENST00000697304.1:c.1621G>T	ENSP00000513240.1:p.Asp541Tyr
ENST00000697306.1:c.*2484G>T	ENSP00000513241.1:n.*2484G>T
ENST00000697307.1:c.1846-2911G>T	ENSP00000513242.1:n.1846-2911G>T
ENST00000697308.1:c.1864G>T	ENSP00000513243.1:p.Asp622Tyr
ENST00000697309.1:c.1933G>T	ENSP00000513244.1:p.Asp645Tyr
ENST00000697310.1:c.1933G>T	ENSP00000513245.1:p.Asp645Tyr
ENST00000697311.1:c.1933G>T	ENSP00000513246.1:p.Asp645Tyr
ENST00000697312.1:c.*1331G>T	ENSP00000513247.1:n.*1331G>T
ENST00000697313.1:n.2688-10665G>T
ENST00000697314.1:n.3636+6967G>T
ENST00000697315.1:c.1933G>T	ENSP00000513248.1:p.Asp645Tyr
ENST00000697316.1:n.2054G>T
ENST00000697317.1:n.2024G>T
ENST00000265433.8:c.1933G>T MANE Select	ENSP00000265433.4:p.Asp645Tyr
ENST00000265433.7:c.1933G>T	ENSP00000265433.3:p.Asp645Tyr
ENST00000396252.6:c.*1806G>T	ENSP00000379551.2:n.*1806G>T
ENST00000409330.5:c.1687G>T	ENSP00000386924.1:p.Asp563Tyr
ENST00000520325.1:n.349G>T
ENST00000613033.1:c.180+1547G>T	ENSP00000484487.1:n.180+1547G>T
NM_001024688.2:c.1687G>T	NP_001019859.1:p.Asp563Tyr
NM_002485.4:c.1933G>T , LRG_158t1:c.1933G>T	NP_002476.2:p.Asp645Tyr
XM_011517044.1:c.1909G>T	XP_011515346.1:p.Asp637Tyr
XM_011517045.1:c.1687G>T	XP_011515347.1:p.Asp563Tyr
XR_928335.1:n.2072G>T
XM_017013460.1:c.1054G>T	XP_016868949.1:p.Asp352Tyr
XM_017013462.2:c.1054G>T	XP_016868951.1:p.Asp352Tyr
XM_024447163.1:c.1687G>T	XP_024302931.1:p.Asp563Tyr
XM_024447164.1:c.1687G>T	XP_024302932.1:p.Asp563Tyr
XM_024447165.1:c.1054G>T	XP_024302933.1:p.Asp352Tyr
NM_002485.5:c.1933G>T MANE Select	NP_002476.2:p.Asp645Tyr
NM_001024688.3:c.1687G>T	NP_001019859.1:p.Asp563Tyr