Canonical Allele Identifier: CA429971834

Gene: SCN2A

Linked Data

• ClinVar Variation Id: 3026212
• ClinVar RCV Id: RCV003884283
• dbSNP Id: rs1698662245
• gnomAD v4: 2-165331331-A-G
• MyVariant Identifiers: chr2:g.166187841A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165331331A>G , CM000664.2:g.165331331A>G	GRCh38
NC_000002.11:g.166187841A>G , CM000664.1:g.166187841A>G	GRCh37
NC_000002.10:g.165896087A>G	NCBI36
NG_008143.1:g.96930A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000631182.3:c.2151A>G MANE Plus Clinical	ENSP00000486885.1:p.Glu717=
ENST00000375437.7:c.2151A>G MANE Select	ENSP00000364586.2:p.Glu717=
ENST00000636071.2:c.2151A>G	ENSP00000490107.1:p.Glu717=
ENST00000636135.1:c.*470A>G	ENSP00000489821.1:n.*470A>G
ENST00000636384.2:c.*138A>G	ENSP00000490765.1:n.*138A>G
ENST00000636662.2:c.*2674A>G	ENSP00000489873.1:n.*2674A>G
ENST00000636769.1:c.*93A>G	ENSP00000490800.1:n.*93A>G
ENST00000636985.2:c.1755A>G	ENSP00000490849.1:p.Glu585=
ENST00000637266.2:c.2151A>G	ENSP00000490866.1:p.Glu717=
ENST00000637367.1:c.*3638A>G	ENSP00000490592.1:n.*3638A>G
ENST00000674133.1:c.2A>G
ENST00000283256.10:c.2151A>G	ENSP00000283256.6:p.Glu717=
ENST00000375427.4:c.2151A>G	ENSP00000364576.2:p.Glu717=
ENST00000375437.6:c.2151A>G	ENSP00000364586.2:p.Glu717=
ENST00000480032.4:n.2294A>G
ENST00000631182.2:c.2151A>G	ENSP00000486885.1:p.Glu717=
NM_001040142.1:c.2151A>G	NP_001035232.1:p.Glu717=
NM_001040143.1:c.2151A>G	NP_001035233.1:p.Glu717=
NM_021007.2:c.2151A>G	NP_066287.2:p.Glu717=
XM_005246750.2:c.2151A>G	XP_005246807.1:p.Glu717=
XM_005246753.2:c.2151A>G	XP_005246810.1:p.Glu717=
XM_005246754.3:c.2121A>G	XP_005246811.1:p.Glu707=
XM_005246755.3:c.1398A>G	XP_005246812.1:p.Glu466=
XM_011511608.1:c.2151A>G	XP_011509910.1:p.Glu717=
XM_011511609.1:c.2151A>G	XP_011509911.1:p.Glu717=
XM_005246753.3:c.2151A>G	XP_005246810.1:p.Glu717=
XM_017004656.1:c.2151A>G	XP_016860145.1:p.Glu717=
XM_017004657.1:c.2151A>G	XP_016860146.1:p.Glu717=
XM_017004658.1:c.1398A>G	XP_016860147.1:p.Glu466=
XM_017004659.1:c.-52A>G	XP_016860148.1:n.-52A>G
XM_024453037.1:c.1398A>G	XP_024308805.1:p.Glu466=
NM_001040142.2:c.2151A>G MANE Select	NP_001035232.1:p.Glu717=
NM_001040143.2:c.2151A>G	NP_001035233.1:p.Glu717=
NM_001371246.1:c.2151A>G MANE Plus Clinical	NP_001358175.1:p.Glu717=
NM_001371247.1:c.2151A>G	NP_001358176.1:p.Glu717=
NM_021007.3:c.2151A>G	NP_066287.2:p.Glu717=