Canonical Allele Identifier: CA1304559623

Gene: SCN2A

Linked Data

• dbSNP Id: rs1701218072

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165374656_165374657dup , CM000664.2:g.165374656_165374657dup	GRCh38
NC_000002.11:g.166231166_166231167dup , CM000664.1:g.166231166_166231167dup	GRCh37
NC_000002.10:g.165939412_165939413dup	NCBI36
NG_008143.1:g.140255_140256dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000631182.3:c.3973-29_3973-28dup MANE Plus Clinical	ENSP00000486885.1:n.3973-29_3973-28dup
ENST00000375437.7:c.3973-29_3973-28dup MANE Select	ENSP00000364586.2:n.3973-29_3973-28dup
ENST00000636071.2:c.3973-29_3973-28dup	ENSP00000490107.1:n.3973-29_3973-28dup
ENST00000636135.1:c.*2292-29_*2292-28dup	ENSP00000489821.1:n.*2292-29_*2292-28dup
ENST00000636384.2:c.*1960-29_*1960-28dup	ENSP00000490765.1:n.*1960-29_*1960-28dup
ENST00000636662.2:c.*4496-29_*4496-28dup	ENSP00000489873.1:n.*4496-29_*4496-28dup
ENST00000636769.1:c.*1915-29_*1915-28dup	ENSP00000490800.1:n.*1915-29_*1915-28dup
ENST00000636985.2:c.3577-29_3577-28dup	ENSP00000490849.1:n.3577-29_3577-28dup
ENST00000637266.2:c.3973-29_3973-28dup	ENSP00000490866.1:n.3973-29_3973-28dup
ENST00000283256.10:c.3973-29_3973-28dup	ENSP00000283256.6:n.3973-29_3973-28dup
ENST00000375427.4:c.3973-29_3973-28dup	ENSP00000364576.2:n.3973-29_3973-28dup
ENST00000375437.6:c.3973-29_3973-28dup	ENSP00000364586.2:n.3973-29_3973-28dup
ENST00000480032.4:n.7041-29_7041-28dup
ENST00000631182.2:c.3973-29_3973-28dup	ENSP00000486885.1:n.3973-29_3973-28dup
NM_001040142.1:c.3973-29_3973-28dup	NP_001035232.1:n.3973-29_3973-28dup
NM_001040143.1:c.3973-29_3973-28dup	NP_001035233.1:n.3973-29_3973-28dup
NM_021007.2:c.3973-29_3973-28dup	NP_066287.2:n.3973-29_3973-28dup
XM_005246750.2:c.3973-29_3973-28dup	XP_005246807.1:n.3973-29_3973-28dup
XM_005246753.2:c.3973-29_3973-28dup	XP_005246810.1:n.3973-29_3973-28dup
XM_005246754.3:c.3943-29_3943-28dup	XP_005246811.1:n.3943-29_3943-28dup
XM_005246755.3:c.3220-29_3220-28dup	XP_005246812.1:n.3220-29_3220-28dup
XM_011511608.1:c.3973-29_3973-28dup	XP_011509910.1:n.3973-29_3973-28dup
XM_011511609.1:c.3973-29_3973-28dup	XP_011509911.1:n.3973-29_3973-28dup
XM_005246753.3:c.3973-29_3973-28dup	XP_005246810.1:n.3973-29_3973-28dup
XM_017004656.1:c.3973-29_3973-28dup	XP_016860145.1:n.3973-29_3973-28dup
XM_017004657.1:c.3973-29_3973-28dup	XP_016860146.1:n.3973-29_3973-28dup
XM_017004658.1:c.3220-29_3220-28dup	XP_016860147.1:n.3220-29_3220-28dup
XM_017004659.1:c.1771-29_1771-28dup	XP_016860148.1:n.1771-29_1771-28dup
XM_024453037.1:c.3220-29_3220-28dup	XP_024308805.1:n.3220-29_3220-28dup
NM_001040142.2:c.3973-29_3973-28dup MANE Select	NP_001035232.1:n.3973-29_3973-28dup
NM_001040143.2:c.3973-29_3973-28dup	NP_001035233.1:n.3973-29_3973-28dup
NM_001371246.1:c.3973-29_3973-28dup MANE Plus Clinical	NP_001358175.1:n.3973-29_3973-28dup
NM_001371247.1:c.3973-29_3973-28dup	NP_001358176.1:n.3973-29_3973-28dup
NM_021007.3:c.3973-29_3973-28dup	NP_066287.2:n.3973-29_3973-28dup