Canonical Allele Identifier: CA384879828

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 3061364
• ClinVar RCV Id: RCV004542679
• MyVariant Identifiers: chr12:g.52145203C>G (hg19) ; chr12:g.51751419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51751419C>G , CM000674.2:g.51751419C>G	GRCh38
NC_000012.11:g.52145203C>G , CM000674.1:g.52145203C>G	GRCh37
NC_000012.10:g.50431470C>G	NCBI36
NG_021180.2:g.165184C>G
NG_021180.3:g.166462C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.2196C>G MANE Plus Clinical	ENSP00000346534.4:p.Ile732Met
ENST00000548086.3:c.43C>G
ENST00000627620.5:c.2196C>G MANE Select	ENSP00000487583.2:p.Ile732Met
ENST00000636945.2:c.200C>G
ENST00000662684.1:c.2196C>G	ENSP00000499636.1:p.Ile732Met
ENST00000668547.1:c.2196C>G	ENSP00000499691.1:p.Ile732Met
ENST00000354534.10:c.2196C>G	ENSP00000346534.4:p.Ile732Met
ENST00000355133.7:c.2196C>G	ENSP00000347255.4:p.Ile732Met
ENST00000545061.5:c.2196C>G	ENSP00000440360.1:p.Ile732Met
ENST00000550891.4:n.2324C>G
ENST00000599343.5:c.2229C>G	ENSP00000476447.3:p.Ile743Met
ENST00000627620.2:c.2196C>G	ENSP00000487583.1:p.Ile732Met
NM_001177984.2:c.2196C>G	NP_001171455.1:p.Ile732Met
NM_014191.3:c.2196C>G	NP_055006.1:p.Ile732Met
XM_006719556.2:c.2196C>G	XP_006719619.1:p.Ile732Met
XM_011538650.1:c.2196C>G	XP_011536952.1:p.Ile732Met
XM_011538651.1:c.2196C>G	XP_011536953.1:p.Ile732Met
NM_001330260.1:c.2196C>G	NP_001317189.1:p.Ile732Met
XM_006719556.4:c.2196C>G	XP_006719619.1:p.Ile732Met
XM_011538651.3:c.2196C>G	XP_011536953.1:p.Ile732Met
XM_017019794.2:c.2196C>G	XP_016875283.1:p.Ile732Met
XM_017019795.2:c.2196C>G	XP_016875284.1:p.Ile732Met
XM_017019796.1:c.2196C>G	XP_016875285.1:p.Ile732Met
NM_001330260.2:c.2196C>G MANE Select	NP_001317189.1:p.Ile732Met
NM_001369788.1:c.2196C>G	NP_001356717.1:p.Ile732Met
NM_014191.4:c.2196C>G MANE Plus Clinical	NP_055006.1:p.Ile732Met
NM_001177984.3:c.2196C>G	NP_001171455.1:p.Ile732Met