Canonical Allele Identifier: CA1304550167

Gene: SCN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165354687_165354690delinsTAAG , CM000664.2:g.165354687_165354690delinsTAAG	GRCh38
NC_000002.11:g.166211197_166211200delinsTAAG , CM000664.1:g.166211197_166211200delinsTAAG	GRCh37
NC_000002.10:g.165919443_165919446delinsTAAG	NCBI36
NG_008143.1:g.120286_120289delinsTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631182.3:c.3399+16_3399+19delinsTAAG MANE Plus Clinical	ENSP00000486885.1:n.3399+16_3399+19delinsTAAG
ENST00000375437.7:c.3399+16_3399+19delinsTAAG MANE Select	ENSP00000364586.2:n.3399+16_3399+19delinsTAAG
ENST00000636071.2:c.3399+16_3399+19delinsTAAG	ENSP00000490107.1:n.3399+16_3399+19delinsTAAG
ENST00000636135.1:c.*1718+16_*1718+19delinsTAAG	ENSP00000489821.1:n.*1718+16_*1718+19delinsTAAG
ENST00000636384.2:c.*1386+16_*1386+19delinsTAAG	ENSP00000490765.1:n.*1386+16_*1386+19delinsTAAG
ENST00000636662.2:c.*3922+16_*3922+19delinsTAAG	ENSP00000489873.1:n.*3922+16_*3922+19delinsTAAG
ENST00000636769.1:c.*1341+16_*1341+19delinsTAAG	ENSP00000490800.1:n.*1341+16_*1341+19delinsTAAG
ENST00000636985.2:c.3003+16_3003+19delinsTAAG	ENSP00000490849.1:n.3003+16_3003+19delinsTAAG
ENST00000637266.2:c.3399+16_3399+19delinsTAAG	ENSP00000490866.1:n.3399+16_3399+19delinsTAAG
ENST00000674133.1:c.1250+16_1250+19delinsTAAG
ENST00000283256.10:c.3399+16_3399+19delinsTAAG	ENSP00000283256.6:n.3399+16_3399+19delinsTAAG
ENST00000375427.4:c.3399+16_3399+19delinsTAAG	ENSP00000364576.2:n.3399+16_3399+19delinsTAAG
ENST00000375437.6:c.3399+16_3399+19delinsTAAG	ENSP00000364586.2:n.3399+16_3399+19delinsTAAG
ENST00000480032.4:n.3542+16_3542+19delinsTAAG
ENST00000631182.2:c.3399+16_3399+19delinsTAAG	ENSP00000486885.1:n.3399+16_3399+19delinsTAAG
NM_001040142.1:c.3399+16_3399+19delinsTAAG	NP_001035232.1:n.3399+16_3399+19delinsTAAG
NM_001040143.1:c.3399+16_3399+19delinsTAAG	NP_001035233.1:n.3399+16_3399+19delinsTAAG
NM_021007.2:c.3399+16_3399+19delinsTAAG	NP_066287.2:n.3399+16_3399+19delinsTAAG
XM_005246750.2:c.3399+16_3399+19delinsTAAG	XP_005246807.1:n.3399+16_3399+19delinsTAAG
XM_005246753.2:c.3399+16_3399+19delinsTAAG	XP_005246810.1:n.3399+16_3399+19delinsTAAG
XM_005246754.3:c.3369+16_3369+19delinsTAAG	XP_005246811.1:n.3369+16_3369+19delinsTAAG
XM_005246755.3:c.2646+16_2646+19delinsTAAG	XP_005246812.1:n.2646+16_2646+19delinsTAAG
XM_011511608.1:c.3399+16_3399+19delinsTAAG	XP_011509910.1:n.3399+16_3399+19delinsTAAG
XM_011511609.1:c.3399+16_3399+19delinsTAAG	XP_011509911.1:n.3399+16_3399+19delinsTAAG
XM_005246753.3:c.3399+16_3399+19delinsTAAG	XP_005246810.1:n.3399+16_3399+19delinsTAAG
XM_017004656.1:c.3399+16_3399+19delinsTAAG	XP_016860145.1:n.3399+16_3399+19delinsTAAG
XM_017004657.1:c.3399+16_3399+19delinsTAAG	XP_016860146.1:n.3399+16_3399+19delinsTAAG
XM_017004658.1:c.2646+16_2646+19delinsTAAG	XP_016860147.1:n.2646+16_2646+19delinsTAAG
XM_017004659.1:c.1197+16_1197+19delinsTAAG	XP_016860148.1:n.1197+16_1197+19delinsTAAG
XM_024453037.1:c.2646+16_2646+19delinsTAAG	XP_024308805.1:n.2646+16_2646+19delinsTAAG
NM_001040142.2:c.3399+16_3399+19delinsTAAG MANE Select	NP_001035232.1:n.3399+16_3399+19delinsTAAG
NM_001040143.2:c.3399+16_3399+19delinsTAAG	NP_001035233.1:n.3399+16_3399+19delinsTAAG
NM_001371246.1:c.3399+16_3399+19delinsTAAG MANE Plus Clinical	NP_001358175.1:n.3399+16_3399+19delinsTAAG
NM_001371247.1:c.3399+16_3399+19delinsTAAG	NP_001358176.1:n.3399+16_3399+19delinsTAAG
NM_021007.3:c.3399+16_3399+19delinsTAAG	NP_066287.2:n.3399+16_3399+19delinsTAAG