Canonical Allele Identifier: CA1304556619

Gene: SCN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165370249C= , CM000664.2:g.165370249C=	GRCh38
NC_000002.11:g.166226759C= , CM000664.1:g.166226759C=	GRCh37
NC_000002.10:g.165935005C=	NCBI36
NG_008143.1:g.135848C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.3799C= MANE Plus Clinical	ENSP00000486885.1:p.Gln1267=
ENST00000375437.7:c.3799C= MANE Select	ENSP00000364586.2:p.Gln1267=
ENST00000636071.2:c.3799C=	ENSP00000490107.1:p.Gln1267=
ENST00000636135.1:c.*2118C=	ENSP00000489821.1:n.*2118C=
ENST00000636384.2:c.*1786C=	ENSP00000490765.1:n.*1786C=
ENST00000636662.2:c.*4322C=	ENSP00000489873.1:n.*4322C=
ENST00000636769.1:c.*1741C=	ENSP00000490800.1:n.*1741C=
ENST00000636985.2:c.3403C=	ENSP00000490849.1:p.Gln1135=
ENST00000637266.2:c.3799C=	ENSP00000490866.1:p.Gln1267=
ENST00000283256.10:c.3799C=	ENSP00000283256.6:p.Gln1267=
ENST00000375427.4:c.3799C=	ENSP00000364576.2:p.Gln1267=
ENST00000375437.6:c.3799C=	ENSP00000364586.2:p.Gln1267=
ENST00000480032.4:n.3942C=
ENST00000631182.2:c.3799C=	ENSP00000486885.1:p.Gln1267=
NM_001040142.1:c.3799C=	NP_001035232.1:p.Gln1267=
NM_001040143.1:c.3799C=	NP_001035233.1:p.Gln1267=
NM_021007.2:c.3799C=	NP_066287.2:p.Gln1267=
XM_005246750.2:c.3799C=	XP_005246807.1:p.Gln1267=
XM_005246753.2:c.3799C=	XP_005246810.1:p.Gln1267=
XM_005246754.3:c.3769C=	XP_005246811.1:p.Gln1257=
XM_005246755.3:c.3046C=	XP_005246812.1:p.Gln1016=
XM_011511608.1:c.3799C=	XP_011509910.1:p.Gln1267=
XM_011511609.1:c.3799C=	XP_011509911.1:p.Gln1267=
XM_005246753.3:c.3799C=	XP_005246810.1:p.Gln1267=
XM_017004656.1:c.3799C=	XP_016860145.1:p.Gln1267=
XM_017004657.1:c.3799C=	XP_016860146.1:p.Gln1267=
XM_017004658.1:c.3046C=	XP_016860147.1:p.Gln1016=
XM_017004659.1:c.1597C=	XP_016860148.1:p.Gln533=
XM_024453037.1:c.3046C=	XP_024308805.1:p.Gln1016=
NM_001040142.2:c.3799C= MANE Select	NP_001035232.1:p.Gln1267=
NM_001040143.2:c.3799C=	NP_001035233.1:p.Gln1267=
NM_001371246.1:c.3799C= MANE Plus Clinical	NP_001358175.1:p.Gln1267=
NM_001371247.1:c.3799C=	NP_001358176.1:p.Gln1267=
NM_021007.3:c.3799C=	NP_066287.2:p.Gln1267=