Canonical Allele Identifier: CA318202
Community Standard Title: NM_001040142.2(SCN2A):c.1526A>G (p.Lys509Arg)
Gene: SCN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165315613A>G , CM000664.2:g.165315613A>G GRCh38
NC_000002.11:g.166172123A>G , CM000664.1:g.166172123A>G GRCh37
NC_000002.10:g.165880369A>G NCBI36
NG_008143.1:g.81212A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001040142.2:c.1526A>G MANE Select NP_001035232.1:p.Lys509Arg
ENST00000375437.7:c.1526A>G MANE Select ENSP00000364586.2:p.Lys509Arg
NM_001371246.1:c.1526A>G MANE Plus Clinical NP_001358175.1:p.Lys509Arg
ENST00000631182.3:c.1526A>G MANE Plus Clinical ENSP00000486885.1:p.Lys509Arg
NM_001040142.1:c.1526A>G NP_001035232.1:p.Lys509Arg
NM_001040143.1:c.1526A>G NP_001035233.1:p.Lys509Arg
NM_001040143.2:c.1526A>G NP_001035233.1:p.Lys509Arg
NM_001371247.1:c.1526A>G NP_001358176.1:p.Lys509Arg
NM_021007.2:c.1526A>G NP_066287.2:p.Lys509Arg
NM_021007.3:c.1526A>G NP_066287.2:p.Lys509Arg
ENST00000283256.10:c.1526A>G ENSP00000283256.6:p.Lys509Arg
ENST00000375427.4:c.1526A>G ENSP00000364576.2:p.Lys509Arg
ENST00000375437.6:c.1526A>G ENSP00000364586.2:p.Lys509Arg
ENST00000480032.4:n.1669A>G
ENST00000631182.2:c.1526A>G ENSP00000486885.1:p.Lys509Arg
ENST00000635945.1:n.1889A>G
ENST00000636071.2:c.1526A>G ENSP00000490107.1:p.Lys509Arg
ENST00000636135.1:c.1397A>G ENSP00000489821.1:p.Lys466Arg
ENST00000636384.2:c.1526A>G ENSP00000490765.1:p.Lys509Arg
ENST00000636662.2:c.*2049A>G ENSP00000489873.1:n.*2049A>G
ENST00000636769.1:c.1526A>G ENSP00000490800.1:p.Lys509Arg
ENST00000636985.2:c.1130A>G ENSP00000490849.1:p.Lys377Arg
ENST00000637266.2:c.1526A>G ENSP00000490866.1:p.Lys509Arg
ENST00000637367.1:c.*1459A>G ENSP00000490592.1:n.*1459A>G
ENST00000638151.1:n.1610A>G
XM_005246750.2:c.1526A>G XP_005246807.1:p.Lys509Arg
XM_005246753.2:c.1526A>G XP_005246810.1:p.Lys509Arg
XM_005246753.3:c.1526A>G XP_005246810.1:p.Lys509Arg
XM_005246754.3:c.1496A>G XP_005246811.1:p.Lys499Arg
XM_005246755.3:c.773A>G XP_005246812.1:p.Lys258Arg
XM_011511608.1:c.1526A>G XP_011509910.1:p.Lys509Arg
XM_011511609.1:c.1526A>G XP_011509911.1:p.Lys509Arg
XM_017004656.1:c.1526A>G XP_016860145.1:p.Lys509Arg
XM_017004657.1:c.1526A>G XP_016860146.1:p.Lys509Arg
XM_017004658.1:c.773A>G XP_016860147.1:p.Lys258Arg
XM_024453037.1:c.773A>G XP_024308805.1:p.Lys258Arg