Canonical Allele Identifier: CA1801419586

Gene: NBN

Linked Data

• dbSNP Id: rs1810190877

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946322_89946323insTTTCAACTGTATCACAAGAGGTC , CM000670.2:g.89946322_89946323insTTTCAACTGTATCACAAGAGGTC	GRCh38
NC_000008.10:g.90958550_90958551insTTTCAACTGTATCACAAGAGGTC , CM000670.1:g.90958550_90958551insTTTCAACTGTATCACAAGAGGTC	GRCh37
NC_000008.9:g.91027726_91027727insTTTCAACTGTATCACAAGAGGTC	NCBI36
NG_008860.1:g.43349_43350insGACCTCTTGTGATACAGTTGAAA , LRG_158:g.43349_43350insGACCTCTTGTGATACAGTTGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3217-28_3217-27insGACCTCTTGTGATACAGTTGAAA
ENST00000517337.2:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000429971.2:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000523444.2:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000428252.2:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697292.1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513229.1:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697293.1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513230.1:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697294.1:c.*1526-28_*1526-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513231.1:n.*1526-28_*1526-27insGACCTCTTGTGATACAGTTGA...
ENST00000697295.1:c.*1224-28_*1224-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513232.1:n.*1224-28_*1224-27insGACCTCTTGTGATACAGTTGA...
ENST00000697296.1:c.*1583-28_*1583-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513233.1:n.*1583-28_*1583-27insGACCTCTTGTGATACAGTTGA...
ENST00000697297.1:n.3700-28_3700-27insGACCTCTTGTGATACAGTTGAAA
ENST00000697298.1:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513234.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697299.1:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513235.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697300.1:c.*1519-28_*1519-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513236.1:n.*1519-28_*1519-27insGACCTCTTGTGATACAGTTGA...
ENST00000697301.1:c.*1436-28_*1436-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513237.1:n.*1436-28_*1436-27insGACCTCTTGTGATACAGTTGA...
ENST00000697302.1:c.*1436-28_*1436-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513238.1:n.*1436-28_*1436-27insGACCTCTTGTGATACAGTTGA...
ENST00000697303.1:c.*1519-28_*1519-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513239.1:n.*1519-28_*1519-27insGACCTCTTGTGATACAGTTGA...
ENST00000697304.1:c.1603-28_1603-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513240.1:n.1603-28_1603-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697306.1:c.*2438_*2439insGACCTCTTGTGATACAGTTGAAA	ENSP00000513241.1:n.*2438_*2439insGACCTCTTGTGATACAGTTGAAA
ENST00000697307.1:c.1846-2957_1846-2956insGACCTCTTGTGATACAGTTGAAA	ENSP00000513242.1:n.1846-2957_1846-2956insGACCTCTTGTGATACAGTT...
ENST00000697308.1:c.1846-28_1846-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513243.1:n.1846-28_1846-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697309.1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513244.1:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697310.1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513245.1:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697311.1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513246.1:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697312.1:c.*1313-28_*1313-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513247.1:n.*1313-28_*1313-27insGACCTCTTGTGATACAGTTGA...
ENST00000697313.1:n.2688-10711_2688-10710insGACCTCTTGTGATACAGTTGAAA
ENST00000697314.1:n.3636+6921_3636+6922insGACCTCTTGTGATACAGTTGAAA
ENST00000697315.1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000513248.1:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000697316.1:n.2036-28_2036-27insGACCTCTTGTGATACAGTTGAAA
ENST00000697317.1:n.2006-28_2006-27insGACCTCTTGTGATACAGTTGAAA
ENST00000265433.8:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA MANE Select	ENSP00000265433.4:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000265433.7:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000265433.3:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000396252.6:c.*1788-28_*1788-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000379551.2:n.*1788-28_*1788-27insGACCTCTTGTGATACAGTTGA...
ENST00000409330.5:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	ENSP00000386924.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA...
ENST00000520325.1:n.303_304insGACCTCTTGTGATACAGTTGAAA
ENST00000613033.1:c.180+1501_180+1502insGACCTCTTGTGATACAGTTGAAA	ENSP00000484487.1:n.180+1501_180+1502insGACCTCTTGTGATACAGTTGA...
NM_001024688.2:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	NP_001019859.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA
NM_002485.4:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA , LRG_158t1:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA	NP_002476.2:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA
XM_011517044.1:c.1891-28_1891-27insGACCTCTTGTGATACAGTTGAAA	XP_011515346.1:n.1891-28_1891-27insGACCTCTTGTGATACAGTTGAAA
XM_011517045.1:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	XP_011515347.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA
XR_928335.1:n.2054-28_2054-27insGACCTCTTGTGATACAGTTGAAA
XM_017013460.1:c.1036-28_1036-27insGACCTCTTGTGATACAGTTGAAA	XP_016868949.1:n.1036-28_1036-27insGACCTCTTGTGATACAGTTGAAA
XM_017013462.2:c.1036-28_1036-27insGACCTCTTGTGATACAGTTGAAA	XP_016868951.1:n.1036-28_1036-27insGACCTCTTGTGATACAGTTGAAA
XM_024447163.1:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	XP_024302931.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA
XM_024447164.1:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	XP_024302932.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA
XM_024447165.1:c.1036-28_1036-27insGACCTCTTGTGATACAGTTGAAA	XP_024302933.1:n.1036-28_1036-27insGACCTCTTGTGATACAGTTGAAA
NM_002485.5:c.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA MANE Select	NP_002476.2:n.1915-28_1915-27insGACCTCTTGTGATACAGTTGAAA
NM_001024688.3:c.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA	NP_001019859.1:n.1669-28_1669-27insGACCTCTTGTGATACAGTTGAAA