Canonical Allele Identifier: CA371655632

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90965776A>C (hg19) ; chr8:g.89953548A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953548A>C , CM000670.2:g.89953548A>C	GRCh38
NC_000008.10:g.90965776A>C , CM000670.1:g.90965776A>C	GRCh37
NC_000008.9:g.91034952A>C	NCBI36
NG_008860.1:g.36124T>G , LRG_158:g.36124T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2843T>G
ENST00000517337.2:c.1295T>G	ENSP00000429971.2:p.Val432Gly
ENST00000523444.2:c.1295T>G	ENSP00000428252.2:p.Val432Gly
ENST00000697292.1:c.1541T>G	ENSP00000513229.1:p.Val514Gly
ENST00000697293.1:c.1541T>G	ENSP00000513230.1:p.Val514Gly
ENST00000697294.1:c.*1152T>G	ENSP00000513231.1:n.*1152T>G
ENST00000697295.1:c.*850T>G	ENSP00000513232.1:n.*850T>G
ENST00000697296.1:c.*1209T>G	ENSP00000513233.1:n.*1209T>G
ENST00000697297.1:n.3326T>G
ENST00000697298.1:c.1295T>G	ENSP00000513234.1:p.Val432Gly
ENST00000697299.1:c.1295T>G	ENSP00000513235.1:p.Val432Gly
ENST00000697300.1:c.*1145T>G	ENSP00000513236.1:n.*1145T>G
ENST00000697301.1:c.*1062T>G	ENSP00000513237.1:n.*1062T>G
ENST00000697302.1:c.*1062T>G	ENSP00000513238.1:n.*1062T>G
ENST00000697303.1:c.*1145T>G	ENSP00000513239.1:n.*1145T>G
ENST00000697304.1:c.1229T>G	ENSP00000513240.1:p.Val410Gly
ENST00000697306.1:c.*541T>G	ENSP00000513241.1:n.*541T>G
ENST00000697307.1:c.1541T>G	ENSP00000513242.1:p.Val514Gly
ENST00000697308.1:c.1541T>G	ENSP00000513243.1:p.Val514Gly
ENST00000697309.1:c.1541T>G	ENSP00000513244.1:p.Val514Gly
ENST00000697310.1:c.1541T>G	ENSP00000513245.1:p.Val514Gly
ENST00000697311.1:c.1541T>G	ENSP00000513246.1:p.Val514Gly
ENST00000697312.1:c.*939T>G	ENSP00000513247.1:n.*939T>G
ENST00000697313.1:n.2687+16816T>G
ENST00000697314.1:n.3332T>G
ENST00000697315.1:c.1541T>G	ENSP00000513248.1:p.Val514Gly
ENST00000697316.1:n.1662T>G
ENST00000697317.1:n.1651T>G
ENST00000697318.1:n.1653T>G
ENST00000265433.8:c.1541T>G MANE Select	ENSP00000265433.4:p.Val514Gly
ENST00000265433.7:c.1541T>G	ENSP00000265433.3:p.Val514Gly
ENST00000396252.6:c.*1414T>G	ENSP00000379551.2:n.*1414T>G
ENST00000409330.5:c.1295T>G	ENSP00000386924.1:p.Val432Gly
NM_001024688.2:c.1295T>G	NP_001019859.1:p.Val432Gly
NM_002485.4:c.1541T>G , LRG_158t1:c.1541T>G	NP_002476.2:p.Val514Gly
XM_011517044.1:c.1517T>G	XP_011515346.1:p.Val506Gly
XM_011517045.1:c.1295T>G	XP_011515347.1:p.Val432Gly
XR_928335.1:n.1680T>G
XM_017013460.1:c.662T>G	XP_016868949.1:p.Val221Gly
XM_017013462.2:c.662T>G	XP_016868951.1:p.Val221Gly
XM_024447163.1:c.1295T>G	XP_024302931.1:p.Val432Gly
XM_024447164.1:c.1295T>G	XP_024302932.1:p.Val432Gly
XM_024447165.1:c.662T>G	XP_024302933.1:p.Val221Gly
NM_002485.5:c.1541T>G MANE Select	NP_002476.2:p.Val514Gly
NM_001024688.3:c.1295T>G	NP_001019859.1:p.Val432Gly