Canonical Allele Identifier: CA349018089

Gene: SCN2A

Linked Data

• ClinVar Variation Id: 1070304
• ClinVar RCV Id: RCV002319707
• dbSNP Id: rs1697364931
• MyVariant Identifiers: chr2:g.166166922G>A (hg19) ; chr2:g.165310412G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165310412G>A , CM000664.2:g.165310412G>A	GRCh38
NC_000002.11:g.166166922G>A , CM000664.1:g.166166922G>A	GRCh37
NC_000002.10:g.165875168G>A	NCBI36
NG_008143.1:g.76011G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000631182.3:c.787G>A MANE Plus Clinical	ENSP00000486885.1:p.Ala263Thr
ENST00000375437.7:c.787G>A MANE Select	ENSP00000364586.2:p.Ala263Thr
ENST00000635945.1:n.1150G>A
ENST00000636071.2:c.787G>A	ENSP00000490107.1:p.Ala263Thr
ENST00000636135.1:c.658G>A	ENSP00000489821.1:p.Ala220Thr
ENST00000636384.2:c.787G>A	ENSP00000490765.1:p.Ala263Thr
ENST00000636662.2:c.*1310G>A	ENSP00000489873.1:n.*1310G>A
ENST00000636769.1:c.787G>A	ENSP00000490800.1:p.Ala263Thr
ENST00000636985.2:c.391G>A	ENSP00000490849.1:p.Ala131Thr
ENST00000637266.2:c.787G>A	ENSP00000490866.1:p.Ala263Thr
ENST00000637367.1:c.*720G>A	ENSP00000490592.1:n.*720G>A
ENST00000638151.1:n.871G>A
ENST00000283256.10:c.787G>A	ENSP00000283256.6:p.Ala263Thr
ENST00000375427.4:c.787G>A	ENSP00000364576.2:p.Ala263Thr
ENST00000375437.6:c.787G>A	ENSP00000364586.2:p.Ala263Thr
ENST00000424833.5:c.787G>A	ENSP00000406454.2:p.Ala263Thr
ENST00000480032.4:n.930G>A
ENST00000486878.2:c.328G>A	ENSP00000487466.1:p.Ala110Thr
ENST00000631182.2:c.787G>A	ENSP00000486885.1:p.Ala263Thr
NM_001040142.1:c.787G>A	NP_001035232.1:p.Ala263Thr
NM_001040143.1:c.787G>A	NP_001035233.1:p.Ala263Thr
NM_021007.2:c.787G>A	NP_066287.2:p.Ala263Thr
XM_005246750.2:c.787G>A	XP_005246807.1:p.Ala263Thr
XM_005246753.2:c.787G>A	XP_005246810.1:p.Ala263Thr
XM_005246754.3:c.757G>A	XP_005246811.1:p.Ala253Thr
XM_005246755.3:c.34G>A	XP_005246812.1:p.Ala12Thr
XM_011511608.1:c.787G>A	XP_011509910.1:p.Ala263Thr
XM_011511609.1:c.787G>A	XP_011509911.1:p.Ala263Thr
XM_005246753.3:c.787G>A	XP_005246810.1:p.Ala263Thr
XM_017004656.1:c.787G>A	XP_016860145.1:p.Ala263Thr
XM_017004657.1:c.787G>A	XP_016860146.1:p.Ala263Thr
XM_017004658.1:c.34G>A	XP_016860147.1:p.Ala12Thr
XM_024453037.1:c.34G>A	XP_024308805.1:p.Ala12Thr
NM_001040142.2:c.787G>A MANE Select	NP_001035232.1:p.Ala263Thr
NM_001040143.2:c.787G>A	NP_001035233.1:p.Ala263Thr
NM_001371246.1:c.787G>A MANE Plus Clinical	NP_001358175.1:p.Ala263Thr
NM_001371247.1:c.787G>A	NP_001358176.1:p.Ala263Thr
NM_021007.3:c.787G>A	NP_066287.2:p.Ala263Thr