Canonical Allele Identifier: CA2687855168

Gene: NBN

Linked Data

• gnomAD v4: 8-89970644-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970644A>G , CM000670.2:g.89970644A>G	GRCh38
NC_000008.10:g.90982872A>G , CM000670.1:g.90982872A>G	GRCh37
NC_000008.9:g.91052048A>G	NCBI36
NG_008860.1:g.19028T>C , LRG_158:g.19028T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2005-87T>C
ENST00000517337.2:c.457-87T>C	ENSP00000429971.2:n.457-87T>C
ENST00000523444.2:c.457-87T>C	ENSP00000428252.2:n.457-87T>C
ENST00000697292.1:c.703-87T>C	ENSP00000513229.1:n.703-87T>C
ENST00000697293.1:c.703-87T>C	ENSP00000513230.1:n.703-87T>C
ENST00000697294.1:c.*314-87T>C	ENSP00000513231.1:n.*314-87T>C
ENST00000697295.1:c.*12-87T>C	ENSP00000513232.1:n.*12-87T>C
ENST00000697296.1:c.*371-87T>C	ENSP00000513233.1:n.*371-87T>C
ENST00000697297.1:n.2488-87T>C
ENST00000697298.1:c.457-87T>C	ENSP00000513234.1:n.457-87T>C
ENST00000697299.1:c.457-87T>C	ENSP00000513235.1:n.457-87T>C
ENST00000697300.1:c.*307-87T>C	ENSP00000513236.1:n.*307-87T>C
ENST00000697301.1:c.*224-87T>C	ENSP00000513237.1:n.*224-87T>C
ENST00000697302.1:c.*224-87T>C	ENSP00000513238.1:n.*224-87T>C
ENST00000697303.1:c.*307-87T>C	ENSP00000513239.1:n.*307-87T>C
ENST00000697304.1:c.585-6137T>C	ENSP00000513240.1:n.585-6137T>C
ENST00000697306.1:c.480+10090T>C	ENSP00000513241.1:n.480+10090T>C
ENST00000697307.1:c.703-87T>C	ENSP00000513242.1:n.703-87T>C
ENST00000697308.1:c.703-87T>C	ENSP00000513243.1:n.703-87T>C
ENST00000697309.1:c.703-87T>C	ENSP00000513244.1:n.703-87T>C
ENST00000697310.1:c.703-87T>C	ENSP00000513245.1:n.703-87T>C
ENST00000697311.1:c.703-87T>C	ENSP00000513246.1:n.703-87T>C
ENST00000697312.1:c.*101-87T>C	ENSP00000513247.1:n.*101-87T>C
ENST00000697313.1:n.2494-87T>C
ENST00000697314.1:n.2494-87T>C
ENST00000697315.1:c.703-87T>C	ENSP00000513248.1:n.703-87T>C
ENST00000697316.1:n.824-87T>C
ENST00000697317.1:n.813-87T>C
ENST00000697318.1:n.815-87T>C
ENST00000265433.8:c.703-87T>C MANE Select	ENSP00000265433.4:n.703-87T>C
ENST00000265433.7:c.703-87T>C	ENSP00000265433.3:n.703-87T>C
ENST00000396252.6:c.*576-87T>C	ENSP00000379551.2:n.*576-87T>C
ENST00000409330.5:c.457-87T>C	ENSP00000386924.1:n.457-87T>C
ENST00000517772.5:c.457-87T>C	ENSP00000428717.1:n.457-87T>C
ENST00000519426.5:c.439-87T>C	ENSP00000430983.1:n.439-87T>C
NM_001024688.2:c.457-87T>C	NP_001019859.1:n.457-87T>C
NM_002485.4:c.703-87T>C , LRG_158t1:c.703-87T>C	NP_002476.2:n.703-87T>C
XM_011517044.1:c.679-87T>C	XP_011515346.1:n.679-87T>C
XM_011517045.1:c.457-87T>C	XP_011515347.1:n.457-87T>C
XM_011517046.1:c.703-87T>C	XP_011515348.1:n.703-87T>C
XR_928335.1:n.840-87T>C
XM_017013460.1:c.-177-87T>C	XP_016868949.1:n.-177-87T>C
XM_017013462.2:c.-177-87T>C	XP_016868951.1:n.-177-87T>C
XM_024447163.1:c.457-87T>C	XP_024302931.1:n.457-87T>C
XM_024447164.1:c.457-87T>C	XP_024302932.1:n.457-87T>C
XM_024447165.1:c.-177-87T>C	XP_024302933.1:n.-177-87T>C
NM_002485.5:c.703-87T>C MANE Select	NP_002476.2:n.703-87T>C
NM_001024688.3:c.457-87T>C	NP_001019859.1:n.457-87T>C