Canonical Allele Identifier: CA371674786

Gene: NBN

Linked Data

• ClinVar Variation Id: 1787759
• ClinVar RCV Id: RCV002425856
• MyVariant Identifiers: chr8:g.90949278T>G (hg19) ; chr8:g.89937050T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89937050T>G , CM000670.2:g.89937050T>G	GRCh38
NC_000008.10:g.90949278T>G , CM000670.1:g.90949278T>G	GRCh37
NC_000008.9:g.91018454T>G	NCBI36
NG_008860.1:g.52622A>C , LRG_158:g.52622A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474821.2:n.3630A>C
ENST00000494804.2:n.3512A>C
ENST00000517337.2:c.1964A>C	ENSP00000429971.2:p.Glu655Ala
ENST00000523444.2:c.1964A>C	ENSP00000428252.2:p.Glu655Ala
ENST00000697292.1:c.2210A>C	ENSP00000513229.1:p.Glu737Ala
ENST00000697293.1:c.2261A>C	ENSP00000513230.1:p.Glu754Ala
ENST00000697294.1:c.*1821A>C	ENSP00000513231.1:n.*1821A>C
ENST00000697295.1:c.*1519A>C	ENSP00000513232.1:n.*1519A>C
ENST00000697296.1:c.*1878A>C	ENSP00000513233.1:n.*1878A>C
ENST00000697297.1:n.3995A>C
ENST00000697298.1:c.1964A>C	ENSP00000513234.1:p.Glu655Ala
ENST00000697299.1:c.1964A>C	ENSP00000513235.1:p.Glu655Ala
ENST00000697300.1:c.*1814A>C	ENSP00000513236.1:n.*1814A>C
ENST00000697301.1:c.*1731A>C	ENSP00000513237.1:n.*1731A>C
ENST00000697302.1:c.*1731A>C	ENSP00000513238.1:n.*1731A>C
ENST00000697303.1:c.*1814A>C	ENSP00000513239.1:n.*1814A>C
ENST00000697304.1:c.1898A>C	ENSP00000513240.1:p.Glu633Ala
ENST00000697305.1:n.2477A>C
ENST00000697306.1:c.*2761A>C	ENSP00000513241.1:n.*2761A>C
ENST00000697307.1:c.1985A>C	ENSP00000513242.1:p.Glu662Ala
ENST00000697308.1:c.2141A>C	ENSP00000513243.1:p.Glu714Ala
ENST00000697309.1:c.2185-1438A>C	ENSP00000513244.1:n.2185-1438A>C
ENST00000697310.1:c.2210A>C	ENSP00000513245.1:p.Glu737Ala
ENST00000697311.1:c.*475A>C	ENSP00000513246.1:n.*475A>C
ENST00000697312.1:c.*1663A>C	ENSP00000513247.1:n.*1663A>C
ENST00000697313.1:n.2688-1438A>C
ENST00000697314.1:n.3637-1438A>C
ENST00000697315.1:c.*114A>C	ENSP00000513248.1:n.*114A>C
ENST00000697316.1:n.2331A>C
ENST00000265433.8:c.2210A>C MANE Select	ENSP00000265433.4:p.Glu737Ala
ENST00000265433.7:c.2210A>C	ENSP00000265433.3:p.Glu737Ala
ENST00000396252.6:c.*2083A>C	ENSP00000379551.2:n.*2083A>C
ENST00000409330.5:c.1964A>C	ENSP00000386924.1:p.Glu655Ala
ENST00000474821.1:n.298A>C
ENST00000613033.1:c.320A>C	ENSP00000484487.1:p.Glu107Ala
NM_001024688.2:c.1964A>C	NP_001019859.1:p.Glu655Ala
NM_002485.4:c.2210A>C , LRG_158t1:c.2210A>C	NP_002476.2:p.Glu737Ala
XM_011517044.1:c.2186A>C	XP_011515346.1:p.Glu729Ala
XM_011517045.1:c.1964A>C	XP_011515347.1:p.Glu655Ala
XM_017013460.1:c.1331A>C	XP_016868949.1:p.Glu444Ala
XM_017013462.2:c.1331A>C	XP_016868951.1:p.Glu444Ala
XM_024447163.1:c.1964A>C	XP_024302931.1:p.Glu655Ala
XM_024447164.1:c.1964A>C	XP_024302932.1:p.Glu655Ala
XM_024447165.1:c.1331A>C	XP_024302933.1:p.Glu444Ala
NM_002485.5:c.2210A>C MANE Select	NP_002476.2:p.Glu737Ala
NM_001024688.3:c.1964A>C	NP_001019859.1:p.Glu655Ala