Canonical Allele Identifier: CA349015905

Gene: SCN2A

Linked Data

• ClinVar Variation Id: 1493037
• ClinVar RCV Id: RCV001984064
• dbSNP Id: rs1346837998
• MyVariant Identifiers: chr2:g.166165185T>A (hg19) ; chr2:g.165308675T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165308675T>A , CM000664.2:g.165308675T>A	GRCh38
NC_000002.11:g.166165185T>A , CM000664.1:g.166165185T>A	GRCh37
NC_000002.10:g.165873431T>A	NCBI36
NG_008143.1:g.74274T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.486T>A MANE Plus Clinical	ENSP00000486885.1:p.Phe162Leu
ENST00000375437.7:c.486T>A MANE Select	ENSP00000364586.2:p.Phe162Leu
ENST00000635945.1:n.849T>A
ENST00000636071.2:c.486T>A	ENSP00000490107.1:p.Phe162Leu
ENST00000636135.1:c.477-677T>A	ENSP00000489821.1:n.477-677T>A
ENST00000636384.2:c.486T>A	ENSP00000490765.1:p.Phe162Leu
ENST00000636662.2:c.*1009T>A	ENSP00000489873.1:n.*1009T>A
ENST00000636769.1:c.486T>A	ENSP00000490800.1:p.Phe162Leu
ENST00000636985.2:c.90T>A	ENSP00000490849.1:p.Phe30Leu
ENST00000637266.2:c.486T>A	ENSP00000490866.1:p.Phe162Leu
ENST00000637367.1:c.*419T>A	ENSP00000490592.1:n.*419T>A
ENST00000638151.1:n.570T>A
ENST00000283256.10:c.486T>A	ENSP00000283256.6:p.Phe162Leu
ENST00000375427.4:c.486T>A	ENSP00000364576.2:p.Phe162Leu
ENST00000375437.6:c.486T>A	ENSP00000364586.2:p.Phe162Leu
ENST00000424833.5:c.486T>A	ENSP00000406454.2:p.Phe162Leu
ENST00000480032.4:n.629T>A
ENST00000486878.2:c.27T>A	ENSP00000487466.1:p.Phe9Leu
ENST00000631182.2:c.486T>A	ENSP00000486885.1:p.Phe162Leu
NM_001040142.1:c.486T>A	NP_001035232.1:p.Phe162Leu
NM_001040143.1:c.486T>A	NP_001035233.1:p.Phe162Leu
NM_021007.2:c.486T>A	NP_066287.2:p.Phe162Leu
XM_005246750.2:c.486T>A	XP_005246807.1:p.Phe162Leu
XM_005246753.2:c.486T>A	XP_005246810.1:p.Phe162Leu
XM_005246754.3:c.456T>A	XP_005246811.1:p.Phe152Leu
XM_011511608.1:c.486T>A	XP_011509910.1:p.Phe162Leu
XM_011511609.1:c.486T>A	XP_011509911.1:p.Phe162Leu
XM_005246753.3:c.486T>A	XP_005246810.1:p.Phe162Leu
XM_017004656.1:c.486T>A	XP_016860145.1:p.Phe162Leu
XM_017004657.1:c.486T>A	XP_016860146.1:p.Phe162Leu
XM_017004658.1:c.-455T>A	XP_016860147.1:n.-455T>A
XM_024453037.1:c.-176T>A	XP_024308805.1:n.-176T>A
NM_001040142.2:c.486T>A MANE Select	NP_001035232.1:p.Phe162Leu
NM_001040143.2:c.486T>A	NP_001035233.1:p.Phe162Leu
NM_001371246.1:c.486T>A MANE Plus Clinical	NP_001358175.1:p.Phe162Leu
NM_001371247.1:c.486T>A	NP_001358176.1:p.Phe162Leu
NM_021007.3:c.486T>A	NP_066287.2:p.Phe162Leu