Canonical Allele Identifier: CA2499221740

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 1219777
• ClinVar RCV Id: RCV001590452
• dbSNP Id: rs2138943001

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51806643del , CM000674.2:g.51806643del	GRCh38
NC_000012.11:g.52200427del , CM000674.1:g.52200427del	GRCh37
NC_000012.10:g.50486694del	NCBI36
NG_021180.2:g.220408del
NG_021180.3:g.221686del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.5157del MANE Plus Clinical	ENSP00000346534.4:p.Asp1720ThrfsTer4
ENST00000627620.5:c.5157del MANE Select	ENSP00000487583.2:p.Asp1720ThrfsTer4
ENST00000636945.2:c.3221del
ENST00000662684.1:c.5157del	ENSP00000499636.1:p.Asp1720ThrfsTer4
ENST00000668547.1:c.5034del	ENSP00000499691.1:p.Asp1679ThrfsTer4
ENST00000354534.10:c.5157del	ENSP00000346534.4:p.Asp1720ThrfsTer4
ENST00000355133.7:c.5034del	ENSP00000347255.4:p.Asp1679ThrfsTer4
ENST00000545061.5:c.5034del	ENSP00000440360.1:p.Asp1679ThrfsTer4
ENST00000599343.5:c.5190del	ENSP00000476447.3:p.Asp1731ThrfsTer4
ENST00000627620.2:c.5157del	ENSP00000487583.1:p.Asp1720ThrfsTer4
NM_001177984.2:c.5034del	NP_001171455.1:p.Asp1679ThrfsTer4
NM_014191.3:c.5157del	NP_055006.1:p.Asp1720ThrfsTer4
XM_006719556.2:c.5157del	XP_006719619.1:p.Asp1720ThrfsTer4
XM_011538650.1:c.5157del	XP_011536952.1:p.Asp1720ThrfsTer4
XM_011538651.1:c.5157del	XP_011536953.1:p.Asp1720ThrfsTer4
NM_001330260.1:c.5157del	NP_001317189.1:p.Asp1720ThrfsTer4
XM_006719556.4:c.5157del	XP_006719619.1:p.Asp1720ThrfsTer4
XM_011538651.3:c.5157del	XP_011536953.1:p.Asp1720ThrfsTer4
XM_017019794.2:c.5157del	XP_016875283.1:p.Asp1720ThrfsTer4
XM_017019795.2:c.5034del	XP_016875284.1:p.Asp1679ThrfsTer4
NM_001330260.2:c.5157del MANE Select	NP_001317189.1:p.Asp1720ThrfsTer4
NM_001369788.1:c.5034del	NP_001356717.1:p.Asp1679ThrfsTer4
NM_014191.4:c.5157del MANE Plus Clinical	NP_055006.1:p.Asp1720ThrfsTer4
NM_001177984.3:c.5034del	NP_001171455.1:p.Asp1679ThrfsTer4