Canonical Allele Identifier: CA1940296

Gene: SCN2A

Linked Data

• dbSNP Id: rs768687355
• ExAC: 2:166243208 A / AT
• gnomAD v2: 2-166243208-A-AT
• gnomAD v3: 2-165386698-A-AT
• gnomAD v4: 2-165386698-A-AT
• MyVariant Identifiers: chr2:g.166243209_166243210insT (hg19) ; chr2:g.166243208_166243209insT (hg19) ; chr2:g.165386699_165386700insT (hg38) ; chr2:g.165386698_165386699insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165386706dup , CM000664.2:g.165386706dup	GRCh38
NC_000002.11:g.166243216dup , CM000664.1:g.166243216dup	GRCh37
NC_000002.10:g.165951462dup	NCBI36
NG_008143.1:g.152305dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000631182.3:c.4552-40dup MANE Plus Clinical	ENSP00000486885.1:n.4552-40dup
ENST00000375437.7:c.4552-40dup MANE Select	ENSP00000364586.2:n.4552-40dup
ENST00000636071.2:c.4552-40dup	ENSP00000490107.1:n.4552-40dup
ENST00000636135.1:c.*2871-40dup	ENSP00000489821.1:n.*2871-40dup
ENST00000636384.2:c.*2539-40dup	ENSP00000490765.1:n.*2539-40dup
ENST00000636662.2:c.*5075-40dup	ENSP00000489873.1:n.*5075-40dup
ENST00000636769.1:c.*2494-40dup	ENSP00000490800.1:n.*2494-40dup
ENST00000636985.2:c.4156-40dup	ENSP00000490849.1:n.4156-40dup
ENST00000637266.2:c.4552-40dup	ENSP00000490866.1:n.4552-40dup
ENST00000283256.10:c.4552-40dup	ENSP00000283256.6:n.4552-40dup
ENST00000375427.4:c.4552-40dup	ENSP00000364576.2:n.4552-40dup
ENST00000375437.6:c.4552-40dup	ENSP00000364586.2:n.4552-40dup
ENST00000480032.4:n.7983-40dup
ENST00000631182.2:c.4552-40dup	ENSP00000486885.1:n.4552-40dup
NM_001040142.1:c.4552-40dup	NP_001035232.1:n.4552-40dup
NM_001040143.1:c.4552-40dup	NP_001035233.1:n.4552-40dup
NM_021007.2:c.4552-40dup	NP_066287.2:n.4552-40dup
XM_005246750.2:c.4552-40dup	XP_005246807.1:n.4552-40dup
XM_005246753.2:c.4552-40dup	XP_005246810.1:n.4552-40dup
XM_005246754.3:c.4522-40dup	XP_005246811.1:n.4522-40dup
XM_005246755.3:c.3799-40dup	XP_005246812.1:n.3799-40dup
XM_011511608.1:c.4552-40dup	XP_011509910.1:n.4552-40dup
XM_011511609.1:c.4552-40dup	XP_011509911.1:n.4552-40dup
XM_005246753.3:c.4552-40dup	XP_005246810.1:n.4552-40dup
XM_017004656.1:c.4552-40dup	XP_016860145.1:n.4552-40dup
XM_017004657.1:c.4552-40dup	XP_016860146.1:n.4552-40dup
XM_017004658.1:c.3799-40dup	XP_016860147.1:n.3799-40dup
XM_017004659.1:c.2350-40dup	XP_016860148.1:n.2350-40dup
XM_024453037.1:c.3799-40dup	XP_024308805.1:n.3799-40dup
NM_001040142.2:c.4552-40dup MANE Select	NP_001035232.1:n.4552-40dup
NM_001040143.2:c.4552-40dup	NP_001035233.1:n.4552-40dup
NM_001371246.1:c.4552-40dup MANE Plus Clinical	NP_001358175.1:n.4552-40dup
NM_001371247.1:c.4552-40dup	NP_001358176.1:n.4552-40dup
NM_021007.3:c.4552-40dup	NP_066287.2:n.4552-40dup