Canonical Allele Identifier: CA10578796

Gene: NBN

Linked Data

• ClinVar Variation Id: 230627
• ClinVar RCV Id: RCV000214158 ; RCV000636800
• dbSNP Id: rs876658674
• gnomAD v2: 8-90983443-T-C
• gnomAD v3: 8-89971215-T-C
• gnomAD v4: 8-89971215-T-C
• MyVariant Identifiers: chr8:g.90983443T>C (hg19) ; chr8:g.89971215T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89971215T>C , CM000670.2:g.89971215T>C	GRCh38
NC_000008.10:g.90983443T>C , CM000670.1:g.90983443T>C	GRCh37
NC_000008.9:g.91052619T>C	NCBI36
NG_008860.1:g.18457A>G , LRG_158:g.18457A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.1962A>G
ENST00000517337.2:c.414A>G	ENSP00000429971.2:p.Gln138=
ENST00000523444.2:c.414A>G	ENSP00000428252.2:p.Gln138=
ENST00000697292.1:c.660A>G	ENSP00000513229.1:p.Gln220=
ENST00000697293.1:c.660A>G	ENSP00000513230.1:p.Gln220=
ENST00000697294.1:c.*271A>G	ENSP00000513231.1:n.*271A>G
ENST00000697295.1:c.113A>G	ENSP00000513232.1:p.Lys38Arg
ENST00000697296.1:c.*328A>G	ENSP00000513233.1:n.*328A>G
ENST00000697297.1:n.2445A>G
ENST00000697298.1:c.414A>G	ENSP00000513234.1:p.Gln138=
ENST00000697299.1:c.414A>G	ENSP00000513235.1:p.Gln138=
ENST00000697300.1:c.*264A>G	ENSP00000513236.1:n.*264A>G
ENST00000697301.1:c.*181A>G	ENSP00000513237.1:n.*181A>G
ENST00000697302.1:c.*181A>G	ENSP00000513238.1:n.*181A>G
ENST00000697303.1:c.*264A>G	ENSP00000513239.1:n.*264A>G
ENST00000697304.1:c.585-6708A>G	ENSP00000513240.1:n.585-6708A>G
ENST00000697306.1:c.480+9519A>G	ENSP00000513241.1:n.480+9519A>G
ENST00000697307.1:c.660A>G	ENSP00000513242.1:p.Gln220=
ENST00000697308.1:c.660A>G	ENSP00000513243.1:p.Gln220=
ENST00000697309.1:c.660A>G	ENSP00000513244.1:p.Gln220=
ENST00000697310.1:c.660A>G	ENSP00000513245.1:p.Gln220=
ENST00000697311.1:c.660A>G	ENSP00000513246.1:p.Gln220=
ENST00000697312.1:c.*58A>G	ENSP00000513247.1:n.*58A>G
ENST00000697313.1:n.2451A>G
ENST00000697314.1:n.2451A>G
ENST00000697315.1:c.660A>G	ENSP00000513248.1:p.Gln220=
ENST00000697316.1:n.781A>G
ENST00000697317.1:n.770A>G
ENST00000697318.1:n.772A>G
ENST00000265433.8:c.660A>G MANE Select	ENSP00000265433.4:p.Gln220=
ENST00000265433.7:c.660A>G	ENSP00000265433.3:p.Gln220=
ENST00000396252.6:c.*533A>G	ENSP00000379551.2:n.*533A>G
ENST00000409330.5:c.414A>G	ENSP00000386924.1:p.Gln138=
ENST00000517772.5:c.414A>G	ENSP00000428717.1:p.Gln138=
ENST00000519426.5:c.396A>G	ENSP00000430983.1:p.Gln132=
NM_001024688.2:c.414A>G	NP_001019859.1:p.Gln138=
NM_002485.4:c.660A>G , LRG_158t1:c.660A>G	NP_002476.2:p.Gln220=
XM_011517044.1:c.636A>G	XP_011515346.1:p.Gln212=
XM_011517045.1:c.414A>G	XP_011515347.1:p.Gln138=
XM_011517046.1:c.660A>G	XP_011515348.1:p.Gln220=
XR_928335.1:n.797A>G
XM_017013460.1:c.-220A>G	XP_016868949.1:n.-220A>G
XM_017013462.2:c.-220A>G	XP_016868951.1:n.-220A>G
XM_024447163.1:c.414A>G	XP_024302931.1:p.Gln138=
XM_024447164.1:c.414A>G	XP_024302932.1:p.Gln138=
XM_024447165.1:c.-220A>G	XP_024302933.1:n.-220A>G
NM_002485.5:c.660A>G MANE Select	NP_002476.2:p.Gln220=
NM_001024688.3:c.414A>G	NP_001019859.1:p.Gln138=