Canonical Allele Identifier: CA1304529988

Gene: SCN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165309431T= , CM000664.2:g.165309431T=	GRCh38
NC_000002.11:g.166165941T= , CM000664.1:g.166165941T=	GRCh37
NC_000002.10:g.165874187T=	NCBI36
NG_008143.1:g.75030T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.697+175T= MANE Plus Clinical	ENSP00000486885.1:n.697+175T=
ENST00000375437.7:c.685T= MANE Select	ENSP00000364586.2:p.Ser229=
ENST00000635945.1:n.1048T=
ENST00000636071.2:c.697+175T=	ENSP00000490107.1:n.697+175T=
ENST00000636135.1:c.556T=	ENSP00000489821.1:p.Ser186=
ENST00000636384.2:c.685T=	ENSP00000490765.1:p.Ser229=
ENST00000636662.2:c.*1208T=	ENSP00000489873.1:n.*1208T=
ENST00000636769.1:c.685T=	ENSP00000490800.1:p.Ser229=
ENST00000636985.2:c.289T=	ENSP00000490849.1:p.Ser97=
ENST00000637266.2:c.685T=	ENSP00000490866.1:p.Ser229=
ENST00000637367.1:c.*618T=	ENSP00000490592.1:n.*618T=
ENST00000638151.1:n.769T=
ENST00000283256.10:c.685T=	ENSP00000283256.6:p.Ser229=
ENST00000375427.4:c.697+175T=	ENSP00000364576.2:n.697+175T=
ENST00000375437.6:c.685T=	ENSP00000364586.2:p.Ser229=
ENST00000424833.5:c.685T=	ENSP00000406454.2:p.Ser229=
ENST00000480032.4:n.828T=
ENST00000486878.2:c.226T=	ENSP00000487466.1:p.Ser76=
ENST00000631182.2:c.697+175T=	ENSP00000486885.1:n.697+175T=
NM_001040142.1:c.685T=	NP_001035232.1:p.Ser229=
NM_001040143.1:c.697+175T=	NP_001035233.1:n.697+175T=
NM_021007.2:c.685T=	NP_066287.2:p.Ser229=
XM_005246750.2:c.685T=	XP_005246807.1:p.Ser229=
XM_005246753.2:c.697+175T=	XP_005246810.1:n.697+175T=
XM_005246754.3:c.655T=	XP_005246811.1:p.Ser219=
XM_005246755.3:c.-57+637T=	XP_005246812.1:n.-57+637T=
XM_011511608.1:c.685T=	XP_011509910.1:p.Ser229=
XM_011511609.1:c.685T=	XP_011509911.1:p.Ser229=
XM_005246753.3:c.697+175T=	XP_005246810.1:n.697+175T=
XM_017004656.1:c.685T=	XP_016860145.1:p.Ser229=
XM_017004657.1:c.697+175T=	XP_016860146.1:n.697+175T=
XM_017004658.1:c.-69T=	XP_016860147.1:n.-69T=
XM_024453037.1:c.-57+637T=	XP_024308805.1:n.-57+637T=
NM_001040142.2:c.685T= MANE Select	NP_001035232.1:p.Ser229=
NM_001040143.2:c.697+175T=	NP_001035233.1:n.697+175T=
NM_001371246.1:c.697+175T= MANE Plus Clinical	NP_001358175.1:n.697+175T=
NM_001371247.1:c.685T=	NP_001358176.1:p.Ser229=
NM_021007.3:c.685T=	NP_066287.2:p.Ser229=