Canonical Allele Identifier: CA371676329

Gene: NBN

Linked Data

• ClinVar Variation Id: 1043858
• ClinVar RCV Id: RCV001348021
• dbSNP Id: rs1563512800
• MyVariant Identifiers: chr8:g.90958375A>G (hg19) ; chr8:g.89946147A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946147A>G , CM000670.2:g.89946147A>G	GRCh38
NC_000008.10:g.90958375A>G , CM000670.1:g.90958375A>G	GRCh37
NC_000008.9:g.91027551A>G	NCBI36
NG_008860.1:g.43525T>C , LRG_158:g.43525T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.3365T>C
ENST00000517337.2:c.1817T>C	ENSP00000429971.2:p.Phe606Ser
ENST00000523444.2:c.1817T>C	ENSP00000428252.2:p.Phe606Ser
ENST00000697292.1:c.2063T>C	ENSP00000513229.1:p.Phe688Ser
ENST00000697293.1:c.2063T>C	ENSP00000513230.1:p.Phe688Ser
ENST00000697294.1:c.*1674T>C	ENSP00000513231.1:n.*1674T>C
ENST00000697295.1:c.*1372T>C	ENSP00000513232.1:n.*1372T>C
ENST00000697296.1:c.*1731T>C	ENSP00000513233.1:n.*1731T>C
ENST00000697297.1:n.3848T>C
ENST00000697298.1:c.1817T>C	ENSP00000513234.1:p.Phe606Ser
ENST00000697299.1:c.1817T>C	ENSP00000513235.1:p.Phe606Ser
ENST00000697300.1:c.*1667T>C	ENSP00000513236.1:n.*1667T>C
ENST00000697301.1:c.*1584T>C	ENSP00000513237.1:n.*1584T>C
ENST00000697302.1:c.*1584T>C	ENSP00000513238.1:n.*1584T>C
ENST00000697303.1:c.*1667T>C	ENSP00000513239.1:n.*1667T>C
ENST00000697304.1:c.1751T>C	ENSP00000513240.1:p.Phe584Ser
ENST00000697306.1:c.*2614T>C	ENSP00000513241.1:n.*2614T>C
ENST00000697307.1:c.1846-2781T>C	ENSP00000513242.1:n.1846-2781T>C
ENST00000697308.1:c.1994T>C	ENSP00000513243.1:p.Phe665Ser
ENST00000697309.1:c.2063T>C	ENSP00000513244.1:p.Phe688Ser
ENST00000697310.1:c.2063T>C	ENSP00000513245.1:p.Phe688Ser
ENST00000697311.1:c.2063T>C	ENSP00000513246.1:p.Phe688Ser
ENST00000697312.1:c.*1461T>C	ENSP00000513247.1:n.*1461T>C
ENST00000697313.1:n.2688-10535T>C
ENST00000697314.1:n.3636+7097T>C
ENST00000697315.1:c.2063T>C	ENSP00000513248.1:p.Phe688Ser
ENST00000697316.1:n.2184T>C
ENST00000697317.1:n.2154T>C
ENST00000265433.8:c.2063T>C MANE Select	ENSP00000265433.4:p.Phe688Ser
ENST00000265433.7:c.2063T>C	ENSP00000265433.3:p.Phe688Ser
ENST00000396252.6:c.*1936T>C	ENSP00000379551.2:n.*1936T>C
ENST00000409330.5:c.1817T>C	ENSP00000386924.1:p.Phe606Ser
ENST00000520325.1:n.479T>C
ENST00000613033.1:c.180+1677T>C	ENSP00000484487.1:n.180+1677T>C
NM_001024688.2:c.1817T>C	NP_001019859.1:p.Phe606Ser
NM_002485.4:c.2063T>C , LRG_158t1:c.2063T>C	NP_002476.2:p.Phe688Ser
XM_011517044.1:c.2039T>C	XP_011515346.1:p.Phe680Ser
XM_011517045.1:c.1817T>C	XP_011515347.1:p.Phe606Ser
XM_017013460.1:c.1184T>C	XP_016868949.1:p.Phe395Ser
XM_017013462.2:c.1184T>C	XP_016868951.1:p.Phe395Ser
XM_024447163.1:c.1817T>C	XP_024302931.1:p.Phe606Ser
XM_024447164.1:c.1817T>C	XP_024302932.1:p.Phe606Ser
XM_024447165.1:c.1184T>C	XP_024302933.1:p.Phe395Ser
NM_002485.5:c.2063T>C MANE Select	NP_002476.2:p.Phe688Ser
NM_001024688.3:c.1817T>C	NP_001019859.1:p.Phe606Ser