Canonical Allele Identifier: CA371656435

Gene: NBN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89955509G>A , CM000670.2:g.89955509G>A	GRCh38
NC_000008.10:g.90967737G>A , CM000670.1:g.90967737G>A	GRCh37
NC_000008.9:g.91036913G>A	NCBI36
NG_008860.1:g.34163C>T , LRG_158:g.34163C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2473C>T
ENST00000517337.2:c.925C>T	ENSP00000429971.2:p.Gln309Ter
ENST00000523444.2:c.925C>T	ENSP00000428252.2:p.Gln309Ter
ENST00000697292.1:c.1171C>T	ENSP00000513229.1:p.Gln391Ter
ENST00000697293.1:c.1171C>T	ENSP00000513230.1:p.Gln391Ter
ENST00000697294.1:c.*782C>T	ENSP00000513231.1:n.*782C>T
ENST00000697295.1:c.*480C>T	ENSP00000513232.1:n.*480C>T
ENST00000697296.1:c.*839C>T	ENSP00000513233.1:n.*839C>T
ENST00000697297.1:n.2956C>T
ENST00000697298.1:c.925C>T	ENSP00000513234.1:p.Gln309Ter
ENST00000697299.1:c.925C>T	ENSP00000513235.1:p.Gln309Ter
ENST00000697300.1:c.*775C>T	ENSP00000513236.1:n.*775C>T
ENST00000697301.1:c.*692C>T	ENSP00000513237.1:n.*692C>T
ENST00000697302.1:c.*692C>T	ENSP00000513238.1:n.*692C>T
ENST00000697303.1:c.*775C>T	ENSP00000513239.1:n.*775C>T
ENST00000697304.1:c.859C>T	ENSP00000513240.1:p.Gln287Ter
ENST00000697306.1:c.*171C>T	ENSP00000513241.1:n.*171C>T
ENST00000697307.1:c.1171C>T	ENSP00000513242.1:p.Gln391Ter
ENST00000697308.1:c.1171C>T	ENSP00000513243.1:p.Gln391Ter
ENST00000697309.1:c.1171C>T	ENSP00000513244.1:p.Gln391Ter
ENST00000697310.1:c.1171C>T	ENSP00000513245.1:p.Gln391Ter
ENST00000697311.1:c.1171C>T	ENSP00000513246.1:p.Gln391Ter
ENST00000697312.1:c.*569C>T	ENSP00000513247.1:n.*569C>T
ENST00000697313.1:n.2687+14855C>T
ENST00000697314.1:n.2962C>T
ENST00000697315.1:c.1171C>T	ENSP00000513248.1:p.Gln391Ter
ENST00000697316.1:n.1292C>T
ENST00000697317.1:n.1281C>T
ENST00000697318.1:n.1283C>T
ENST00000265433.8:c.1171C>T MANE Select	ENSP00000265433.4:p.Gln391Ter
ENST00000265433.7:c.1171C>T	ENSP00000265433.3:p.Gln391Ter
ENST00000396252.6:c.*1044C>T	ENSP00000379551.2:n.*1044C>T
ENST00000409330.5:c.925C>T	ENSP00000386924.1:p.Gln309Ter
NM_001024688.2:c.925C>T	NP_001019859.1:p.Gln309Ter
NM_002485.4:c.1171C>T , LRG_158t1:c.1171C>T	NP_002476.2:p.Gln391Ter
XM_011517044.1:c.1147C>T	XP_011515346.1:p.Gln383Ter
XM_011517045.1:c.925C>T	XP_011515347.1:p.Gln309Ter
XM_011517046.1:c.1171C>T	XP_011515348.1:p.Gln391Ter
XR_928335.1:n.1308C>T
XM_017013460.1:c.292C>T	XP_016868949.1:p.Gln98Ter
XM_017013462.2:c.292C>T	XP_016868951.1:p.Gln98Ter
XM_024447163.1:c.925C>T	XP_024302931.1:p.Gln309Ter
XM_024447164.1:c.925C>T	XP_024302932.1:p.Gln309Ter
XM_024447165.1:c.292C>T	XP_024302933.1:p.Gln98Ter
NM_002485.5:c.1171C>T MANE Select	NP_002476.2:p.Gln391Ter
NM_001024688.3:c.925C>T	NP_001019859.1:p.Gln309Ter