Canonical Allele Identifier: CA335799

Gene: NBN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946231C>G , CM000670.2:g.89946231C>G	GRCh38
NC_000008.10:g.90958459C>G , CM000670.1:g.90958459C>G	GRCh37
NC_000008.9:g.91027635C>G	NCBI36
NG_008860.1:g.43441G>C , LRG_158:g.43441G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3281G>C
ENST00000517337.2:c.1733G>C	ENSP00000429971.2:p.Arg578Thr
ENST00000523444.2:c.1733G>C	ENSP00000428252.2:p.Arg578Thr
ENST00000697292.1:c.1979G>C	ENSP00000513229.1:p.Arg660Thr
ENST00000697293.1:c.1979G>C	ENSP00000513230.1:p.Arg660Thr
ENST00000697294.1:c.*1590G>C	ENSP00000513231.1:n.*1590G>C
ENST00000697295.1:c.*1288G>C	ENSP00000513232.1:n.*1288G>C
ENST00000697296.1:c.*1647G>C	ENSP00000513233.1:n.*1647G>C
ENST00000697297.1:n.3764G>C
ENST00000697298.1:c.1733G>C	ENSP00000513234.1:p.Arg578Thr
ENST00000697299.1:c.1733G>C	ENSP00000513235.1:p.Arg578Thr
ENST00000697300.1:c.*1583G>C	ENSP00000513236.1:n.*1583G>C
ENST00000697301.1:c.*1500G>C	ENSP00000513237.1:n.*1500G>C
ENST00000697302.1:c.*1500G>C	ENSP00000513238.1:n.*1500G>C
ENST00000697303.1:c.*1583G>C	ENSP00000513239.1:n.*1583G>C
ENST00000697304.1:c.1667G>C	ENSP00000513240.1:p.Arg556Thr
ENST00000697306.1:c.*2530G>C	ENSP00000513241.1:n.*2530G>C
ENST00000697307.1:c.1846-2865G>C	ENSP00000513242.1:n.1846-2865G>C
ENST00000697308.1:c.1910G>C	ENSP00000513243.1:p.Arg637Thr
ENST00000697309.1:c.1979G>C	ENSP00000513244.1:p.Arg660Thr
ENST00000697310.1:c.1979G>C	ENSP00000513245.1:p.Arg660Thr
ENST00000697311.1:c.1979G>C	ENSP00000513246.1:p.Arg660Thr
ENST00000697312.1:c.*1377G>C	ENSP00000513247.1:n.*1377G>C
ENST00000697313.1:n.2688-10619G>C
ENST00000697314.1:n.3636+7013G>C
ENST00000697315.1:c.1979G>C	ENSP00000513248.1:p.Arg660Thr
ENST00000697316.1:n.2100G>C
ENST00000697317.1:n.2070G>C
ENST00000265433.8:c.1979G>C MANE Select	ENSP00000265433.4:p.Arg660Thr
ENST00000265433.7:c.1979G>C	ENSP00000265433.3:p.Arg660Thr
ENST00000396252.6:c.*1852G>C	ENSP00000379551.2:n.*1852G>C
ENST00000409330.5:c.1733G>C	ENSP00000386924.1:p.Arg578Thr
ENST00000520325.1:n.395G>C
ENST00000613033.1:c.180+1593G>C	ENSP00000484487.1:n.180+1593G>C
NM_001024688.2:c.1733G>C	NP_001019859.1:p.Arg578Thr
NM_002485.4:c.1979G>C , LRG_158t1:c.1979G>C	NP_002476.2:p.Arg660Thr
XM_011517044.1:c.1955G>C	XP_011515346.1:p.Arg652Thr
XM_011517045.1:c.1733G>C	XP_011515347.1:p.Arg578Thr
XM_017013460.1:c.1100G>C	XP_016868949.1:p.Arg367Thr
XM_017013462.2:c.1100G>C	XP_016868951.1:p.Arg367Thr
XM_024447163.1:c.1733G>C	XP_024302931.1:p.Arg578Thr
XM_024447164.1:c.1733G>C	XP_024302932.1:p.Arg578Thr
XM_024447165.1:c.1100G>C	XP_024302933.1:p.Arg367Thr
NM_002485.5:c.1979G>C MANE Select	NP_002476.2:p.Arg660Thr
NM_001024688.3:c.1733G>C	NP_001019859.1:p.Arg578Thr