Canonical Allele Identifier: CA239346
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 193734
ClinVar RCV Id: RCV000364025
dbSNP Id: rs794727003
MyVariant Identifiers: chr2:g.166170413C>A (hg19) chr2:g.165313903C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165313903C>A , CM000664.2:g.165313903C>A GRCh38
NC_000002.11:g.166170413C>A , CM000664.1:g.166170413C>A GRCh37
NC_000002.10:g.165878659C>A NCBI36
NG_008143.1:g.79502C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000631182.3:c.1178C>A MANE Plus Clinical ENSP00000486885.1:p.Thr393Lys
ENST00000375437.7:c.1178C>A MANE Select ENSP00000364586.2:p.Thr393Lys
ENST00000635945.1:n.1541C>A
ENST00000636071.2:c.1178C>A ENSP00000490107.1:p.Thr393Lys
ENST00000636135.1:c.1049C>A ENSP00000489821.1:p.Thr350Lys
ENST00000636384.2:c.1178C>A ENSP00000490765.1:p.Thr393Lys
ENST00000636662.2:c.*1701C>A ENSP00000489873.1:n.*1701C>A
ENST00000636769.1:c.1178C>A ENSP00000490800.1:p.Thr393Lys
ENST00000636985.2:c.782C>A ENSP00000490849.1:p.Thr261Lys
ENST00000637266.2:c.1178C>A ENSP00000490866.1:p.Thr393Lys
ENST00000637367.1:c.*1111C>A ENSP00000490592.1:n.*1111C>A
ENST00000638151.1:n.1262C>A
ENST00000283256.10:c.1178C>A ENSP00000283256.6:p.Thr393Lys
ENST00000375427.4:c.1178C>A ENSP00000364576.2:p.Thr393Lys
ENST00000375437.6:c.1178C>A ENSP00000364586.2:p.Thr393Lys
ENST00000424833.5:c.1178C>A ENSP00000406454.2:p.Thr393Lys
ENST00000480032.4:n.1321C>A
ENST00000631182.2:c.1178C>A ENSP00000486885.1:p.Thr393Lys
NM_001040142.1:c.1178C>A NP_001035232.1:p.Thr393Lys
NM_001040143.1:c.1178C>A NP_001035233.1:p.Thr393Lys
NM_021007.2:c.1178C>A NP_066287.2:p.Thr393Lys
XM_005246750.2:c.1178C>A XP_005246807.1:p.Thr393Lys
XM_005246753.2:c.1178C>A XP_005246810.1:p.Thr393Lys
XM_005246754.3:c.1148C>A XP_005246811.1:p.Thr383Lys
XM_005246755.3:c.425C>A XP_005246812.1:p.Thr142Lys
XM_011511608.1:c.1178C>A XP_011509910.1:p.Thr393Lys
XM_011511609.1:c.1178C>A XP_011509911.1:p.Thr393Lys
XM_005246753.3:c.1178C>A XP_005246810.1:p.Thr393Lys
XM_017004656.1:c.1178C>A XP_016860145.1:p.Thr393Lys
XM_017004657.1:c.1178C>A XP_016860146.1:p.Thr393Lys
XM_017004658.1:c.425C>A XP_016860147.1:p.Thr142Lys
XM_024453037.1:c.425C>A XP_024308805.1:p.Thr142Lys
NM_001040142.2:c.1178C>A MANE Select NP_001035232.1:p.Thr393Lys
NM_001040143.2:c.1178C>A NP_001035233.1:p.Thr393Lys
NM_001371246.1:c.1178C>A MANE Plus Clinical NP_001358175.1:p.Thr393Lys
NM_001371247.1:c.1178C>A NP_001358176.1:p.Thr393Lys
NM_021007.3:c.1178C>A NP_066287.2:p.Thr393Lys
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