Canonical Allele Identifier: CA4802649

Gene: NBN

Linked Data

• dbSNP Id: rs749585864
• ExAC: 8:90958565 T / TTC
• gnomAD v2: 8-90958565-T-TTC
• MyVariant Identifiers: chr8:g.90958565_90958566insTC (hg19) ; chr8:g.90958566_90958570delinsTCAACAA (hg19) ; chr8:g.89946337_89946338insTC (hg38) ; chr8:g.89946338_89946342delinsTCAACAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946337_89946338insTC , CM000670.2:g.89946337_89946338insTC	GRCh38
NC_000008.10:g.90958565_90958566insTC , CM000670.1:g.90958565_90958566insTC	GRCh37
NC_000008.9:g.91027741_91027742insTC	NCBI36
NG_008860.1:g.43334_43335insGA , LRG_158:g.43334_43335insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3217-43_3217-42insGA
ENST00000517337.2:c.1669-43_1669-42insGA	ENSP00000429971.2:n.1669-43_1669-42insGA
ENST00000523444.2:c.1669-43_1669-42insGA	ENSP00000428252.2:n.1669-43_1669-42insGA
ENST00000697292.1:c.1915-43_1915-42insGA	ENSP00000513229.1:n.1915-43_1915-42insGA
ENST00000697293.1:c.1915-43_1915-42insGA	ENSP00000513230.1:n.1915-43_1915-42insGA
ENST00000697294.1:c.*1526-43_*1526-42insGA	ENSP00000513231.1:n.*1526-43_*1526-42insGA
ENST00000697295.1:c.*1224-43_*1224-42insGA	ENSP00000513232.1:n.*1224-43_*1224-42insGA
ENST00000697296.1:c.*1583-43_*1583-42insGA	ENSP00000513233.1:n.*1583-43_*1583-42insGA
ENST00000697297.1:n.3700-43_3700-42insGA
ENST00000697298.1:c.1669-43_1669-42insGA	ENSP00000513234.1:n.1669-43_1669-42insGA
ENST00000697299.1:c.1669-43_1669-42insGA	ENSP00000513235.1:n.1669-43_1669-42insGA
ENST00000697300.1:c.*1519-43_*1519-42insGA	ENSP00000513236.1:n.*1519-43_*1519-42insGA
ENST00000697301.1:c.*1436-43_*1436-42insGA	ENSP00000513237.1:n.*1436-43_*1436-42insGA
ENST00000697302.1:c.*1436-43_*1436-42insGA	ENSP00000513238.1:n.*1436-43_*1436-42insGA
ENST00000697303.1:c.*1519-43_*1519-42insGA	ENSP00000513239.1:n.*1519-43_*1519-42insGA
ENST00000697304.1:c.1603-43_1603-42insGA	ENSP00000513240.1:n.1603-43_1603-42insGA
ENST00000697306.1:c.*2423_*2424insGA	ENSP00000513241.1:n.*2423_*2424insGA
ENST00000697307.1:c.1846-2972_1846-2971insGA	ENSP00000513242.1:n.1846-2972_1846-2971insGA
ENST00000697308.1:c.1846-43_1846-42insGA	ENSP00000513243.1:n.1846-43_1846-42insGA
ENST00000697309.1:c.1915-43_1915-42insGA	ENSP00000513244.1:n.1915-43_1915-42insGA
ENST00000697310.1:c.1915-43_1915-42insGA	ENSP00000513245.1:n.1915-43_1915-42insGA
ENST00000697311.1:c.1915-43_1915-42insGA	ENSP00000513246.1:n.1915-43_1915-42insGA
ENST00000697312.1:c.*1313-43_*1313-42insGA	ENSP00000513247.1:n.*1313-43_*1313-42insGA
ENST00000697313.1:n.2688-10726_2688-10725insGA
ENST00000697314.1:n.3636+6906_3636+6907insGA
ENST00000697315.1:c.1915-43_1915-42insGA	ENSP00000513248.1:n.1915-43_1915-42insGA
ENST00000697316.1:n.2036-43_2036-42insGA
ENST00000697317.1:n.2006-43_2006-42insGA
ENST00000265433.8:c.1915-43_1915-42insGA MANE Select	ENSP00000265433.4:n.1915-43_1915-42insGA
ENST00000265433.7:c.1915-43_1915-42insGA	ENSP00000265433.3:n.1915-43_1915-42insGA
ENST00000396252.6:c.*1788-43_*1788-42insGA	ENSP00000379551.2:n.*1788-43_*1788-42insGA
ENST00000409330.5:c.1669-43_1669-42insGA	ENSP00000386924.1:n.1669-43_1669-42insGA
ENST00000520325.1:n.288_289insGA
ENST00000613033.1:c.180+1486_180+1487insGA	ENSP00000484487.1:n.180+1486_180+1487insGA
NM_001024688.2:c.1669-43_1669-42insGA	NP_001019859.1:n.1669-43_1669-42insGA
NM_002485.4:c.1915-43_1915-42insGA , LRG_158t1:c.1915-43_1915-42insGA	NP_002476.2:n.1915-43_1915-42insGA
XM_011517044.1:c.1891-43_1891-42insGA	XP_011515346.1:n.1891-43_1891-42insGA
XM_011517045.1:c.1669-43_1669-42insGA	XP_011515347.1:n.1669-43_1669-42insGA
XR_928335.1:n.2054-43_2054-42insGA
XM_017013460.1:c.1036-43_1036-42insGA	XP_016868949.1:n.1036-43_1036-42insGA
XM_017013462.2:c.1036-43_1036-42insGA	XP_016868951.1:n.1036-43_1036-42insGA
XM_024447163.1:c.1669-43_1669-42insGA	XP_024302931.1:n.1669-43_1669-42insGA
XM_024447164.1:c.1669-43_1669-42insGA	XP_024302932.1:n.1669-43_1669-42insGA
XM_024447165.1:c.1036-43_1036-42insGA	XP_024302933.1:n.1036-43_1036-42insGA
NM_002485.5:c.1915-43_1915-42insGA MANE Select	NP_002476.2:n.1915-43_1915-42insGA
NM_001024688.3:c.1669-43_1669-42insGA	NP_001019859.1:n.1669-43_1669-42insGA