Canonical Allele Identifier: CA16612646

Gene: NBN

Linked Data

• ClinVar Variation Id: 411787
• ClinVar RCV Id: RCV000470877 ; RCV000563097
• dbSNP Id: rs986903713
• MyVariant Identifiers: chr8:g.90955527G>C (hg19) ; chr8:g.89943299G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89943299G>C , CM000670.2:g.89943299G>C	GRCh38
NC_000008.10:g.90955527G>C , CM000670.1:g.90955527G>C	GRCh37
NC_000008.9:g.91024703G>C	NCBI36
NG_008860.1:g.46373C>G , LRG_158:g.46373C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3440C>G
ENST00000517337.2:c.1892C>G	ENSP00000429971.2:p.Ala631Gly
ENST00000523444.2:c.1892C>G	ENSP00000428252.2:p.Ala631Gly
ENST00000697292.1:c.2138C>G	ENSP00000513229.1:p.Ala713Gly
ENST00000697293.1:c.2138C>G	ENSP00000513230.1:p.Ala713Gly
ENST00000697294.1:c.*1749C>G	ENSP00000513231.1:n.*1749C>G
ENST00000697295.1:c.*1447C>G	ENSP00000513232.1:n.*1447C>G
ENST00000697296.1:c.*1806C>G	ENSP00000513233.1:n.*1806C>G
ENST00000697297.1:n.3923C>G
ENST00000697298.1:c.1892C>G	ENSP00000513234.1:p.Ala631Gly
ENST00000697299.1:c.1892C>G	ENSP00000513235.1:p.Ala631Gly
ENST00000697300.1:c.*1742C>G	ENSP00000513236.1:n.*1742C>G
ENST00000697301.1:c.*1659C>G	ENSP00000513237.1:n.*1659C>G
ENST00000697302.1:c.*1659C>G	ENSP00000513238.1:n.*1659C>G
ENST00000697303.1:c.*1742C>G	ENSP00000513239.1:n.*1742C>G
ENST00000697304.1:c.1826C>G	ENSP00000513240.1:p.Ala609Gly
ENST00000697305.1:n.2405C>G
ENST00000697306.1:c.*2689C>G	ENSP00000513241.1:n.*2689C>G
ENST00000697307.1:c.1913C>G	ENSP00000513242.1:p.Ala638Gly
ENST00000697308.1:c.2069C>G	ENSP00000513243.1:p.Ala690Gly
ENST00000697309.1:c.2138C>G	ENSP00000513244.1:p.Ala713Gly
ENST00000697310.1:c.2138C>G	ENSP00000513245.1:p.Ala713Gly
ENST00000697311.1:c.2138C>G	ENSP00000513246.1:p.Ala713Gly
ENST00000697312.1:c.*1536C>G	ENSP00000513247.1:n.*1536C>G
ENST00000697313.1:n.2688-7687C>G
ENST00000697314.1:n.3637-7687C>G
ENST00000697315.1:c.2138C>G	ENSP00000513248.1:p.Ala713Gly
ENST00000697316.1:n.2259C>G
ENST00000265433.8:c.2138C>G MANE Select	ENSP00000265433.4:p.Ala713Gly
ENST00000265433.7:c.2138C>G	ENSP00000265433.3:p.Ala713Gly
ENST00000396252.6:c.*2011C>G	ENSP00000379551.2:n.*2011C>G
ENST00000409330.5:c.1892C>G	ENSP00000386924.1:p.Ala631Gly
ENST00000613033.1:c.248C>G	ENSP00000484487.1:p.Ala83Gly
NM_001024688.2:c.1892C>G	NP_001019859.1:p.Ala631Gly
NM_002485.4:c.2138C>G , LRG_158t1:c.2138C>G	NP_002476.2:p.Ala713Gly
XM_011517044.1:c.2114C>G	XP_011515346.1:p.Ala705Gly
XM_011517045.1:c.1892C>G	XP_011515347.1:p.Ala631Gly
XM_017013460.1:c.1259C>G	XP_016868949.1:p.Ala420Gly
XM_017013462.2:c.1259C>G	XP_016868951.1:p.Ala420Gly
XM_024447163.1:c.1892C>G	XP_024302931.1:p.Ala631Gly
XM_024447164.1:c.1892C>G	XP_024302932.1:p.Ala631Gly
XM_024447165.1:c.1259C>G	XP_024302933.1:p.Ala420Gly
NM_002485.5:c.2138C>G MANE Select	NP_002476.2:p.Ala713Gly
NM_001024688.3:c.1892C>G	NP_001019859.1:p.Ala631Gly