Canonical Allele Identifier: CA2687855012

Gene: NBN

Linked Data

• gnomAD v4: 8-89970249-CAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970259_89970261del , CM000670.2:g.89970259_89970261del	GRCh38
NC_000008.10:g.90982487_90982489del , CM000670.1:g.90982487_90982489del	GRCh37
NC_000008.9:g.91051663_91051665del	NCBI36
NG_008860.1:g.19420_19422del , LRG_158:g.19420_19422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2198+112_2198+114del
ENST00000517337.2:c.650+112_650+114del	ENSP00000429971.2:n.650+112_650+114del
ENST00000523444.2:c.650+112_650+114del	ENSP00000428252.2:n.650+112_650+114del
ENST00000697292.1:c.896+112_896+114del	ENSP00000513229.1:n.896+112_896+114del
ENST00000697293.1:c.896+112_896+114del	ENSP00000513230.1:n.896+112_896+114del
ENST00000697294.1:c.*507+112_*507+114del	ENSP00000513231.1:n.*507+112_*507+114del
ENST00000697295.1:c.*205+112_*205+114del	ENSP00000513232.1:n.*205+112_*205+114del
ENST00000697296.1:c.*564+112_*564+114del	ENSP00000513233.1:n.*564+112_*564+114del
ENST00000697297.1:n.2681+112_2681+114del
ENST00000697298.1:c.650+112_650+114del	ENSP00000513234.1:n.650+112_650+114del
ENST00000697299.1:c.650+112_650+114del	ENSP00000513235.1:n.650+112_650+114del
ENST00000697300.1:c.*500+112_*500+114del	ENSP00000513236.1:n.*500+112_*500+114del
ENST00000697301.1:c.*417+112_*417+114del	ENSP00000513237.1:n.*417+112_*417+114del
ENST00000697302.1:c.*417+112_*417+114del	ENSP00000513238.1:n.*417+112_*417+114del
ENST00000697303.1:c.*500+112_*500+114del	ENSP00000513239.1:n.*500+112_*500+114del
ENST00000697304.1:c.585-5745_585-5743del	ENSP00000513240.1:n.585-5745_585-5743del
ENST00000697306.1:c.480+10482_480+10484del	ENSP00000513241.1:n.480+10482_480+10484del
ENST00000697307.1:c.896+112_896+114del	ENSP00000513242.1:n.896+112_896+114del
ENST00000697308.1:c.896+112_896+114del	ENSP00000513243.1:n.896+112_896+114del
ENST00000697309.1:c.896+112_896+114del	ENSP00000513244.1:n.896+112_896+114del
ENST00000697310.1:c.896+112_896+114del	ENSP00000513245.1:n.896+112_896+114del
ENST00000697311.1:c.896+112_896+114del	ENSP00000513246.1:n.896+112_896+114del
ENST00000697312.1:c.*294+112_*294+114del	ENSP00000513247.1:n.*294+112_*294+114del
ENST00000697313.1:n.2687+112_2687+114del
ENST00000697314.1:n.2687+112_2687+114del
ENST00000697315.1:c.896+112_896+114del	ENSP00000513248.1:n.896+112_896+114del
ENST00000697316.1:n.1017+112_1017+114del
ENST00000697317.1:n.1006+112_1006+114del
ENST00000697318.1:n.1008+112_1008+114del
ENST00000265433.8:c.896+112_896+114del MANE Select	ENSP00000265433.4:n.896+112_896+114del
ENST00000265433.7:c.896+112_896+114del	ENSP00000265433.3:n.896+112_896+114del
ENST00000396252.6:c.*769+112_*769+114del	ENSP00000379551.2:n.*769+112_*769+114del
ENST00000409330.5:c.650+112_650+114del	ENSP00000386924.1:n.650+112_650+114del
NM_001024688.2:c.650+112_650+114del	NP_001019859.1:n.650+112_650+114del
NM_002485.4:c.896+112_896+114del , LRG_158t1:c.896+112_896+114del	NP_002476.2:n.896+112_896+114del
XM_011517044.1:c.872+112_872+114del	XP_011515346.1:n.872+112_872+114del
XM_011517045.1:c.650+112_650+114del	XP_011515347.1:n.650+112_650+114del
XM_011517046.1:c.896+112_896+114del	XP_011515348.1:n.896+112_896+114del
XR_928335.1:n.1033+112_1033+114del
XM_017013460.1:c.17+112_17+114del	XP_016868949.1:n.17+112_17+114del
XM_017013462.2:c.17+112_17+114del	XP_016868951.1:n.17+112_17+114del
XM_024447163.1:c.650+112_650+114del	XP_024302931.1:n.650+112_650+114del
XM_024447164.1:c.650+112_650+114del	XP_024302932.1:n.650+112_650+114del
XM_024447165.1:c.17+112_17+114del	XP_024302933.1:n.17+112_17+114del
NM_002485.5:c.896+112_896+114del MANE Select	NP_002476.2:n.896+112_896+114del
NM_001024688.3:c.650+112_650+114del	NP_001019859.1:n.650+112_650+114del