Canonical Allele Identifier: CA349019468

Gene: SCN2A

Linked Data

• MyVariant Identifiers: chr2:g.166210738T>G (hg19) ; chr2:g.165354228T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165354228T>G , CM000664.2:g.165354228T>G	GRCh38
NC_000002.11:g.166210738T>G , CM000664.1:g.166210738T>G	GRCh37
NC_000002.10:g.165918984T>G	NCBI36
NG_008143.1:g.119827T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.2956T>G MANE Plus Clinical	ENSP00000486885.1:p.Phe986Val
ENST00000375437.7:c.2956T>G MANE Select	ENSP00000364586.2:p.Phe986Val
ENST00000636071.2:c.2956T>G	ENSP00000490107.1:p.Phe986Val
ENST00000636135.1:c.*1275T>G	ENSP00000489821.1:n.*1275T>G
ENST00000636384.2:c.*943T>G	ENSP00000490765.1:n.*943T>G
ENST00000636662.2:c.*3479T>G	ENSP00000489873.1:n.*3479T>G
ENST00000636769.1:c.*898T>G	ENSP00000490800.1:n.*898T>G
ENST00000636985.2:c.2560T>G	ENSP00000490849.1:p.Phe854Val
ENST00000637266.2:c.2956T>G	ENSP00000490866.1:p.Phe986Val
ENST00000673831.1:c.702T>G	ENSP00000501305.1:n.702T>G
ENST00000673883.1:c.521T>G	ENSP00000501309.1:n.521T>G
ENST00000674133.1:c.807T>G
ENST00000283256.10:c.2956T>G	ENSP00000283256.6:p.Phe986Val
ENST00000375427.4:c.2956T>G	ENSP00000364576.2:p.Phe986Val
ENST00000375437.6:c.2956T>G	ENSP00000364586.2:p.Phe986Val
ENST00000480032.4:n.3099T>G
ENST00000631182.2:c.2956T>G	ENSP00000486885.1:p.Phe986Val
NM_001040142.1:c.2956T>G	NP_001035232.1:p.Phe986Val
NM_001040143.1:c.2956T>G	NP_001035233.1:p.Phe986Val
NM_021007.2:c.2956T>G	NP_066287.2:p.Phe986Val
XM_005246750.2:c.2956T>G	XP_005246807.1:p.Phe986Val
XM_005246753.2:c.2956T>G	XP_005246810.1:p.Phe986Val
XM_005246754.3:c.2926T>G	XP_005246811.1:p.Phe976Val
XM_005246755.3:c.2203T>G	XP_005246812.1:p.Phe735Val
XM_011511608.1:c.2956T>G	XP_011509910.1:p.Phe986Val
XM_011511609.1:c.2956T>G	XP_011509911.1:p.Phe986Val
XM_005246753.3:c.2956T>G	XP_005246810.1:p.Phe986Val
XM_017004656.1:c.2956T>G	XP_016860145.1:p.Phe986Val
XM_017004657.1:c.2956T>G	XP_016860146.1:p.Phe986Val
XM_017004658.1:c.2203T>G	XP_016860147.1:p.Phe735Val
XM_017004659.1:c.754T>G	XP_016860148.1:p.Phe252Val
XM_024453037.1:c.2203T>G	XP_024308805.1:p.Phe735Val
NM_001040142.2:c.2956T>G MANE Select	NP_001035232.1:p.Phe986Val
NM_001040143.2:c.2956T>G	NP_001035233.1:p.Phe986Val
NM_001371246.1:c.2956T>G MANE Plus Clinical	NP_001358175.1:p.Phe986Val
NM_001371247.1:c.2956T>G	NP_001358176.1:p.Phe986Val
NM_021007.3:c.2956T>G	NP_066287.2:p.Phe986Val