Canonical Allele Identifier: CA461830782

Gene: NBN

Linked Data

• ClinVar Variation Id: 1084209
• ClinVar RCV Id: RCV001401177
• dbSNP Id: rs2129827145
• MyVariant Identifiers: chr8:g.90982603A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970375A>G , CM000670.2:g.89970375A>G	GRCh38
NC_000008.10:g.90982603A>G , CM000670.1:g.90982603A>G	GRCh37
NC_000008.9:g.91051779A>G	NCBI36
NG_008860.1:g.19297T>C , LRG_158:g.19297T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2187T>C
ENST00000517337.2:c.639T>C	ENSP00000429971.2:p.Asp213=
ENST00000523444.2:c.639T>C	ENSP00000428252.2:p.Asp213=
ENST00000697292.1:c.885T>C	ENSP00000513229.1:p.Asp295=
ENST00000697293.1:c.885T>C	ENSP00000513230.1:p.Asp295=
ENST00000697294.1:c.*496T>C	ENSP00000513231.1:n.*496T>C
ENST00000697295.1:c.*194T>C	ENSP00000513232.1:n.*194T>C
ENST00000697296.1:c.*553T>C	ENSP00000513233.1:n.*553T>C
ENST00000697297.1:n.2670T>C
ENST00000697298.1:c.639T>C	ENSP00000513234.1:p.Asp213=
ENST00000697299.1:c.639T>C	ENSP00000513235.1:p.Asp213=
ENST00000697300.1:c.*489T>C	ENSP00000513236.1:n.*489T>C
ENST00000697301.1:c.*406T>C	ENSP00000513237.1:n.*406T>C
ENST00000697302.1:c.*406T>C	ENSP00000513238.1:n.*406T>C
ENST00000697303.1:c.*489T>C	ENSP00000513239.1:n.*489T>C
ENST00000697304.1:c.585-5868T>C	ENSP00000513240.1:n.585-5868T>C
ENST00000697306.1:c.480+10359T>C	ENSP00000513241.1:n.480+10359T>C
ENST00000697307.1:c.885T>C	ENSP00000513242.1:p.Asp295=
ENST00000697308.1:c.885T>C	ENSP00000513243.1:p.Asp295=
ENST00000697309.1:c.885T>C	ENSP00000513244.1:p.Asp295=
ENST00000697310.1:c.885T>C	ENSP00000513245.1:p.Asp295=
ENST00000697311.1:c.885T>C	ENSP00000513246.1:p.Asp295=
ENST00000697312.1:c.*283T>C	ENSP00000513247.1:n.*283T>C
ENST00000697313.1:n.2676T>C
ENST00000697314.1:n.2676T>C
ENST00000697315.1:c.885T>C	ENSP00000513248.1:p.Asp295=
ENST00000697316.1:n.1006T>C
ENST00000697317.1:n.995T>C
ENST00000697318.1:n.997T>C
ENST00000265433.8:c.885T>C MANE Select	ENSP00000265433.4:p.Asp295=
ENST00000265433.7:c.885T>C	ENSP00000265433.3:p.Asp295=
ENST00000396252.6:c.*758T>C	ENSP00000379551.2:n.*758T>C
ENST00000409330.5:c.639T>C	ENSP00000386924.1:p.Asp213=
NM_001024688.2:c.639T>C	NP_001019859.1:p.Asp213=
NM_002485.4:c.885T>C , LRG_158t1:c.885T>C	NP_002476.2:p.Asp295=
XM_011517044.1:c.861T>C	XP_011515346.1:p.Asp287=
XM_011517045.1:c.639T>C	XP_011515347.1:p.Asp213=
XM_011517046.1:c.885T>C	XP_011515348.1:p.Asp295=
XR_928335.1:n.1022T>C
XM_017013460.1:c.6T>C	XP_016868949.1:p.Asp2=
XM_017013462.2:c.6T>C	XP_016868951.1:p.Asp2=
XM_024447163.1:c.639T>C	XP_024302931.1:p.Asp213=
XM_024447164.1:c.639T>C	XP_024302932.1:p.Asp213=
XM_024447165.1:c.6T>C	XP_024302933.1:p.Asp2=
NM_002485.5:c.885T>C MANE Select	NP_002476.2:p.Asp295=
NM_001024688.3:c.639T>C	NP_001019859.1:p.Asp213=