Canonical Allele Identifier: CA371655799

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90965854G>A (hg19) ; chr8:g.89953626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89953626G>A , CM000670.2:g.89953626G>A	GRCh38
NC_000008.10:g.90965854G>A , CM000670.1:g.90965854G>A	GRCh37
NC_000008.9:g.91035030G>A	NCBI36
NG_008860.1:g.36046C>T , LRG_158:g.36046C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.2765C>T
ENST00000517337.2:c.1217C>T	ENSP00000429971.2:p.Ser406Phe
ENST00000523444.2:c.1217C>T	ENSP00000428252.2:p.Ser406Phe
ENST00000697292.1:c.1463C>T	ENSP00000513229.1:p.Ser488Phe
ENST00000697293.1:c.1463C>T	ENSP00000513230.1:p.Ser488Phe
ENST00000697294.1:c.*1074C>T	ENSP00000513231.1:n.*1074C>T
ENST00000697295.1:c.*772C>T	ENSP00000513232.1:n.*772C>T
ENST00000697296.1:c.*1131C>T	ENSP00000513233.1:n.*1131C>T
ENST00000697297.1:n.3248C>T
ENST00000697298.1:c.1217C>T	ENSP00000513234.1:p.Ser406Phe
ENST00000697299.1:c.1217C>T	ENSP00000513235.1:p.Ser406Phe
ENST00000697300.1:c.*1067C>T	ENSP00000513236.1:n.*1067C>T
ENST00000697301.1:c.*984C>T	ENSP00000513237.1:n.*984C>T
ENST00000697302.1:c.*984C>T	ENSP00000513238.1:n.*984C>T
ENST00000697303.1:c.*1067C>T	ENSP00000513239.1:n.*1067C>T
ENST00000697304.1:c.1151C>T	ENSP00000513240.1:p.Ser384Phe
ENST00000697306.1:c.*463C>T	ENSP00000513241.1:n.*463C>T
ENST00000697307.1:c.1463C>T	ENSP00000513242.1:p.Ser488Phe
ENST00000697308.1:c.1463C>T	ENSP00000513243.1:p.Ser488Phe
ENST00000697309.1:c.1463C>T	ENSP00000513244.1:p.Ser488Phe
ENST00000697310.1:c.1463C>T	ENSP00000513245.1:p.Ser488Phe
ENST00000697311.1:c.1463C>T	ENSP00000513246.1:p.Ser488Phe
ENST00000697312.1:c.*861C>T	ENSP00000513247.1:n.*861C>T
ENST00000697313.1:n.2687+16738C>T
ENST00000697314.1:n.3254C>T
ENST00000697315.1:c.1463C>T	ENSP00000513248.1:p.Ser488Phe
ENST00000697316.1:n.1584C>T
ENST00000697317.1:n.1573C>T
ENST00000697318.1:n.1575C>T
ENST00000265433.8:c.1463C>T MANE Select	ENSP00000265433.4:p.Ser488Phe
ENST00000265433.7:c.1463C>T	ENSP00000265433.3:p.Ser488Phe
ENST00000396252.6:c.*1336C>T	ENSP00000379551.2:n.*1336C>T
ENST00000409330.5:c.1217C>T	ENSP00000386924.1:p.Ser406Phe
NM_001024688.2:c.1217C>T	NP_001019859.1:p.Ser406Phe
NM_002485.4:c.1463C>T , LRG_158t1:c.1463C>T	NP_002476.2:p.Ser488Phe
XM_011517044.1:c.1439C>T	XP_011515346.1:p.Ser480Phe
XM_011517045.1:c.1217C>T	XP_011515347.1:p.Ser406Phe
XR_928335.1:n.1602C>T
XM_017013460.1:c.584C>T	XP_016868949.1:p.Ser195Phe
XM_017013462.2:c.584C>T	XP_016868951.1:p.Ser195Phe
XM_024447163.1:c.1217C>T	XP_024302931.1:p.Ser406Phe
XM_024447164.1:c.1217C>T	XP_024302932.1:p.Ser406Phe
XM_024447165.1:c.584C>T	XP_024302933.1:p.Ser195Phe
NM_002485.5:c.1463C>T MANE Select	NP_002476.2:p.Ser488Phe
NM_001024688.3:c.1217C>T	NP_001019859.1:p.Ser406Phe