Canonical Allele Identifier: CA2687854988

Gene: NBN

Linked Data

• gnomAD v4: 8-89970238-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970238A>T , CM000670.2:g.89970238A>T	GRCh38
NC_000008.10:g.90982466A>T , CM000670.1:g.90982466A>T	GRCh37
NC_000008.9:g.91051642A>T	NCBI36
NG_008860.1:g.19434T>A , LRG_158:g.19434T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2198+126T>A
ENST00000517337.2:c.650+126T>A	ENSP00000429971.2:n.650+126T>A
ENST00000523444.2:c.650+126T>A	ENSP00000428252.2:n.650+126T>A
ENST00000697292.1:c.896+126T>A	ENSP00000513229.1:n.896+126T>A
ENST00000697293.1:c.896+126T>A	ENSP00000513230.1:n.896+126T>A
ENST00000697294.1:c.*507+126T>A	ENSP00000513231.1:n.*507+126T>A
ENST00000697295.1:c.*205+126T>A	ENSP00000513232.1:n.*205+126T>A
ENST00000697296.1:c.*564+126T>A	ENSP00000513233.1:n.*564+126T>A
ENST00000697297.1:n.2681+126T>A
ENST00000697298.1:c.650+126T>A	ENSP00000513234.1:n.650+126T>A
ENST00000697299.1:c.650+126T>A	ENSP00000513235.1:n.650+126T>A
ENST00000697300.1:c.*500+126T>A	ENSP00000513236.1:n.*500+126T>A
ENST00000697301.1:c.*417+126T>A	ENSP00000513237.1:n.*417+126T>A
ENST00000697302.1:c.*417+126T>A	ENSP00000513238.1:n.*417+126T>A
ENST00000697303.1:c.*500+126T>A	ENSP00000513239.1:n.*500+126T>A
ENST00000697304.1:c.585-5731T>A	ENSP00000513240.1:n.585-5731T>A
ENST00000697306.1:c.480+10496T>A	ENSP00000513241.1:n.480+10496T>A
ENST00000697307.1:c.896+126T>A	ENSP00000513242.1:n.896+126T>A
ENST00000697308.1:c.896+126T>A	ENSP00000513243.1:n.896+126T>A
ENST00000697309.1:c.896+126T>A	ENSP00000513244.1:n.896+126T>A
ENST00000697310.1:c.896+126T>A	ENSP00000513245.1:n.896+126T>A
ENST00000697311.1:c.896+126T>A	ENSP00000513246.1:n.896+126T>A
ENST00000697312.1:c.*294+126T>A	ENSP00000513247.1:n.*294+126T>A
ENST00000697313.1:n.2687+126T>A
ENST00000697314.1:n.2687+126T>A
ENST00000697315.1:c.896+126T>A	ENSP00000513248.1:n.896+126T>A
ENST00000697316.1:n.1017+126T>A
ENST00000697317.1:n.1006+126T>A
ENST00000697318.1:n.1008+126T>A
ENST00000265433.8:c.896+126T>A MANE Select	ENSP00000265433.4:n.896+126T>A
ENST00000265433.7:c.896+126T>A	ENSP00000265433.3:n.896+126T>A
ENST00000396252.6:c.*769+126T>A	ENSP00000379551.2:n.*769+126T>A
ENST00000409330.5:c.650+126T>A	ENSP00000386924.1:n.650+126T>A
NM_001024688.2:c.650+126T>A	NP_001019859.1:n.650+126T>A
NM_002485.4:c.896+126T>A , LRG_158t1:c.896+126T>A	NP_002476.2:n.896+126T>A
XM_011517044.1:c.872+126T>A	XP_011515346.1:n.872+126T>A
XM_011517045.1:c.650+126T>A	XP_011515347.1:n.650+126T>A
XM_011517046.1:c.896+126T>A	XP_011515348.1:n.896+126T>A
XR_928335.1:n.1033+126T>A
XM_017013460.1:c.17+126T>A	XP_016868949.1:n.17+126T>A
XM_017013462.2:c.17+126T>A	XP_016868951.1:n.17+126T>A
XM_024447163.1:c.650+126T>A	XP_024302931.1:n.650+126T>A
XM_024447164.1:c.650+126T>A	XP_024302932.1:n.650+126T>A
XM_024447165.1:c.17+126T>A	XP_024302933.1:n.17+126T>A
NM_002485.5:c.896+126T>A MANE Select	NP_002476.2:n.896+126T>A
NM_001024688.3:c.650+126T>A	NP_001019859.1:n.650+126T>A