Canonical Allele Identifier: CA371662959

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90994967A>C (hg19) ; chr8:g.89982739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89982739A>C , CM000670.2:g.89982739A>C	GRCh38
NC_000008.10:g.90994967A>C , CM000670.1:g.90994967A>C	GRCh37
NC_000008.9:g.91064143A>C	NCBI36
NG_008860.1:g.6933T>G , LRG_158:g.6933T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.258T>G
ENST00000517337.2:c.-143T>G	ENSP00000429971.2:n.-143T>G
ENST00000523444.2:c.-143T>G	ENSP00000428252.2:n.-143T>G
ENST00000697292.1:c.154T>G	ENSP00000513229.1:p.Phe52Val
ENST00000697293.1:c.154T>G	ENSP00000513230.1:p.Phe52Val
ENST00000697294.1:c.154T>G	ENSP00000513231.1:p.Phe52Val
ENST00000697295.1:c.37+1786T>G	ENSP00000513232.1:n.37+1786T>G
ENST00000697296.1:c.154T>G	ENSP00000513233.1:p.Phe52Val
ENST00000697297.1:n.260T>G
ENST00000697298.1:c.-143T>G	ENSP00000513234.1:n.-143T>G
ENST00000697299.1:c.-75-1216T>G	ENSP00000513235.1:n.-75-1216T>G
ENST00000697300.1:c.-143T>G	ENSP00000513236.1:n.-143T>G
ENST00000697301.1:c.-143T>G	ENSP00000513237.1:n.-143T>G
ENST00000697302.1:c.154T>G	ENSP00000513238.1:p.Phe52Val
ENST00000697303.1:c.154T>G	ENSP00000513239.1:p.Phe52Val
ENST00000697304.1:c.154T>G	ENSP00000513240.1:p.Phe52Val
ENST00000697306.1:c.154T>G	ENSP00000513241.1:p.Phe52Val
ENST00000697307.1:c.154T>G	ENSP00000513242.1:p.Phe52Val
ENST00000697308.1:c.154T>G	ENSP00000513243.1:p.Phe52Val
ENST00000697309.1:c.154T>G	ENSP00000513244.1:p.Phe52Val
ENST00000697310.1:c.154T>G	ENSP00000513245.1:p.Phe52Val
ENST00000697311.1:c.154T>G	ENSP00000513246.1:p.Phe52Val
ENST00000697312.1:c.154T>G	ENSP00000513247.1:p.Phe52Val
ENST00000697313.1:n.266T>G
ENST00000697314.1:n.266T>G
ENST00000697315.1:c.154T>G	ENSP00000513248.1:p.Phe52Val
ENST00000697316.1:n.275T>G
ENST00000697317.1:n.264T>G
ENST00000697318.1:n.266T>G
ENST00000265433.8:c.154T>G MANE Select	ENSP00000265433.4:p.Phe52Val
ENST00000265433.7:c.154T>G	ENSP00000265433.3:p.Phe52Val
ENST00000396252.6:c.154T>G	ENSP00000379551.2:p.Phe52Val
ENST00000409330.5:c.-93T>G	ENSP00000386924.1:n.-93T>G
ENST00000494804.1:n.258T>G
ENST00000517337.1:c.-143T>G	ENSP00000429971.1:n.-143T>G
ENST00000519426.5:c.154T>G	ENSP00000430983.1:p.Phe52Val
ENST00000523444.1:c.154T>G	ENSP00000428252.1:p.Phe52Val
NM_001024688.2:c.-143T>G	NP_001019859.1:n.-143T>G
NM_002485.4:c.154T>G , LRG_158t1:c.154T>G	NP_002476.2:p.Phe52Val
XM_011517044.1:c.130T>G	XP_011515346.1:p.Phe44Val
XM_011517045.1:c.-143T>G	XP_011515347.1:n.-143T>G
XM_011517046.1:c.154T>G	XP_011515348.1:p.Phe52Val
XR_928335.1:n.291T>G
XM_017013460.1:c.-866T>G	XP_016868949.1:n.-866T>G
XM_017013462.2:c.-672T>G	XP_016868951.1:n.-672T>G
XM_024447163.1:c.-93T>G	XP_024302931.1:n.-93T>G
XM_024447165.1:c.-816T>G	XP_024302933.1:n.-816T>G
NM_002485.5:c.154T>G MANE Select	NP_002476.2:p.Phe52Val
NM_001024688.3:c.-143T>G	NP_001019859.1:n.-143T>G