Canonical Allele Identifier: CA371658240

Gene: NBN

Linked Data

• MyVariant Identifiers: chr8:g.90982607A>T (hg19) ; chr8:g.89970379A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89970379A>T , CM000670.2:g.89970379A>T	GRCh38
NC_000008.10:g.90982607A>T , CM000670.1:g.90982607A>T	GRCh37
NC_000008.9:g.91051783A>T	NCBI36
NG_008860.1:g.19293T>A , LRG_158:g.19293T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.2183T>A
ENST00000517337.2:c.635T>A	ENSP00000429971.2:p.Met212Lys
ENST00000523444.2:c.635T>A	ENSP00000428252.2:p.Met212Lys
ENST00000697292.1:c.881T>A	ENSP00000513229.1:p.Met294Lys
ENST00000697293.1:c.881T>A	ENSP00000513230.1:p.Met294Lys
ENST00000697294.1:c.*492T>A	ENSP00000513231.1:n.*492T>A
ENST00000697295.1:c.*190T>A	ENSP00000513232.1:n.*190T>A
ENST00000697296.1:c.*549T>A	ENSP00000513233.1:n.*549T>A
ENST00000697297.1:n.2666T>A
ENST00000697298.1:c.635T>A	ENSP00000513234.1:p.Met212Lys
ENST00000697299.1:c.635T>A	ENSP00000513235.1:p.Met212Lys
ENST00000697300.1:c.*485T>A	ENSP00000513236.1:n.*485T>A
ENST00000697301.1:c.*402T>A	ENSP00000513237.1:n.*402T>A
ENST00000697302.1:c.*402T>A	ENSP00000513238.1:n.*402T>A
ENST00000697303.1:c.*485T>A	ENSP00000513239.1:n.*485T>A
ENST00000697304.1:c.585-5872T>A	ENSP00000513240.1:n.585-5872T>A
ENST00000697306.1:c.480+10355T>A	ENSP00000513241.1:n.480+10355T>A
ENST00000697307.1:c.881T>A	ENSP00000513242.1:p.Met294Lys
ENST00000697308.1:c.881T>A	ENSP00000513243.1:p.Met294Lys
ENST00000697309.1:c.881T>A	ENSP00000513244.1:p.Met294Lys
ENST00000697310.1:c.881T>A	ENSP00000513245.1:p.Met294Lys
ENST00000697311.1:c.881T>A	ENSP00000513246.1:p.Met294Lys
ENST00000697312.1:c.*279T>A	ENSP00000513247.1:n.*279T>A
ENST00000697313.1:n.2672T>A
ENST00000697314.1:n.2672T>A
ENST00000697315.1:c.881T>A	ENSP00000513248.1:p.Met294Lys
ENST00000697316.1:n.1002T>A
ENST00000697317.1:n.991T>A
ENST00000697318.1:n.993T>A
ENST00000265433.8:c.881T>A MANE Select	ENSP00000265433.4:p.Met294Lys
ENST00000265433.7:c.881T>A	ENSP00000265433.3:p.Met294Lys
ENST00000396252.6:c.*754T>A	ENSP00000379551.2:n.*754T>A
ENST00000409330.5:c.635T>A	ENSP00000386924.1:p.Met212Lys
NM_001024688.2:c.635T>A	NP_001019859.1:p.Met212Lys
NM_002485.4:c.881T>A , LRG_158t1:c.881T>A	NP_002476.2:p.Met294Lys
XM_011517044.1:c.857T>A	XP_011515346.1:p.Met286Lys
XM_011517045.1:c.635T>A	XP_011515347.1:p.Met212Lys
XM_011517046.1:c.881T>A	XP_011515348.1:p.Met294Lys
XR_928335.1:n.1018T>A
XM_017013460.1:c.2T>A	XP_016868949.1:p.Met1Lys
XM_017013462.2:c.2T>A	XP_016868951.1:p.Met1Lys
XM_024447163.1:c.635T>A	XP_024302931.1:p.Met212Lys
XM_024447164.1:c.635T>A	XP_024302932.1:p.Met212Lys
XM_024447165.1:c.2T>A	XP_024302933.1:p.Met1Lys
NM_002485.5:c.881T>A MANE Select	NP_002476.2:p.Met294Lys
NM_001024688.3:c.635T>A	NP_001019859.1:p.Met212Lys