Canonical Allele Identifier: CA349021247

Gene: SCN2A

Linked Data

• MyVariant Identifiers: chr2:g.166170255A>T (hg19) ; chr2:g.165313745A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165313745A>T , CM000664.2:g.165313745A>T	GRCh38
NC_000002.11:g.166170255A>T , CM000664.1:g.166170255A>T	GRCh37
NC_000002.10:g.165878501A>T	NCBI36
NG_008143.1:g.79344A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.1160A>T MANE Plus Clinical	ENSP00000486885.1:p.Glu387Val
ENST00000375437.7:c.1160A>T MANE Select	ENSP00000364586.2:p.Glu387Val
ENST00000635945.1:n.1523A>T
ENST00000636071.2:c.1160A>T	ENSP00000490107.1:p.Glu387Val
ENST00000636135.1:c.1031A>T	ENSP00000489821.1:p.Glu344Val
ENST00000636384.2:c.1160A>T	ENSP00000490765.1:p.Glu387Val
ENST00000636662.2:c.*1683A>T	ENSP00000489873.1:n.*1683A>T
ENST00000636769.1:c.1160A>T	ENSP00000490800.1:p.Glu387Val
ENST00000636985.2:c.764A>T	ENSP00000490849.1:p.Glu255Val
ENST00000637266.2:c.1160A>T	ENSP00000490866.1:p.Glu387Val
ENST00000637367.1:c.*1093A>T	ENSP00000490592.1:n.*1093A>T
ENST00000638151.1:n.1244A>T
ENST00000283256.10:c.1160A>T	ENSP00000283256.6:p.Glu387Val
ENST00000375427.4:c.1160A>T	ENSP00000364576.2:p.Glu387Val
ENST00000375437.6:c.1160A>T	ENSP00000364586.2:p.Glu387Val
ENST00000424833.5:c.1160A>T	ENSP00000406454.2:p.Glu387Val
ENST00000480032.4:n.1303A>T
ENST00000631182.2:c.1160A>T	ENSP00000486885.1:p.Glu387Val
NM_001040142.1:c.1160A>T	NP_001035232.1:p.Glu387Val
NM_001040143.1:c.1160A>T	NP_001035233.1:p.Glu387Val
NM_021007.2:c.1160A>T	NP_066287.2:p.Glu387Val
XM_005246750.2:c.1160A>T	XP_005246807.1:p.Glu387Val
XM_005246753.2:c.1160A>T	XP_005246810.1:p.Glu387Val
XM_005246754.3:c.1130A>T	XP_005246811.1:p.Glu377Val
XM_005246755.3:c.407A>T	XP_005246812.1:p.Glu136Val
XM_011511608.1:c.1160A>T	XP_011509910.1:p.Glu387Val
XM_011511609.1:c.1160A>T	XP_011509911.1:p.Glu387Val
XM_005246753.3:c.1160A>T	XP_005246810.1:p.Glu387Val
XM_017004656.1:c.1160A>T	XP_016860145.1:p.Glu387Val
XM_017004657.1:c.1160A>T	XP_016860146.1:p.Glu387Val
XM_017004658.1:c.407A>T	XP_016860147.1:p.Glu136Val
XM_024453037.1:c.407A>T	XP_024308805.1:p.Glu136Val
NM_001040142.2:c.1160A>T MANE Select	NP_001035232.1:p.Glu387Val
NM_001040143.2:c.1160A>T	NP_001035233.1:p.Glu387Val
NM_001371246.1:c.1160A>T MANE Plus Clinical	NP_001358175.1:p.Glu387Val
NM_001371247.1:c.1160A>T	NP_001358176.1:p.Glu387Val
NM_021007.3:c.1160A>T	NP_066287.2:p.Glu387Val