Canonical Allele Identifier: CA10586286

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 253277
• ClinVar RCV Id: RCV000239741 ; RCV001854934
• dbSNP Id: rs879255695
• MyVariant Identifiers: chr12:g.52082570A>G (hg19) ; chr12:g.51688786A>G (hg38)
• PubMed: PMID:25533962 ; PMID:25568300 ; PMID:27559564 ; PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51688786A>G , CM000674.2:g.51688786A>G	GRCh38
NC_000012.11:g.52082570A>G , CM000674.1:g.52082570A>G	GRCh37
NC_000012.10:g.50368837A>G	NCBI36
NG_021180.2:g.102551A>G
NG_021180.3:g.103829A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703687.1:n.2410A>G
ENST00000354534.11:c.643A>G MANE Plus Clinical	ENSP00000346534.4:p.Asn215Asp
ENST00000627620.5:c.615-219A>G MANE Select	ENSP00000487583.2:n.615-219A>G
ENST00000637709.2:c.643A>G	ENSP00000490470.1:p.Asn215Asp
ENST00000638820.1:c.615-219A>G	ENSP00000492157.1:n.615-219A>G
ENST00000662684.1:c.615-219A>G	ENSP00000499636.1:n.615-219A>G
ENST00000667214.1:c.643A>G	ENSP00000499724.1:p.Asn215Asp
ENST00000668547.1:c.615-219A>G	ENSP00000499691.1:n.615-219A>G
ENST00000354534.10:c.643A>G	ENSP00000346534.4:p.Asn215Asp
ENST00000355133.7:c.643A>G	ENSP00000347255.4:p.Asn215Asp
ENST00000545061.5:c.643A>G	ENSP00000440360.1:p.Asn215Asp
ENST00000550891.4:n.743-219A>G
ENST00000551216.2:c.165-219A>G	ENSP00000447567.2:n.165-219A>G
ENST00000599343.5:c.643A>G	ENSP00000476447.3:p.Asn215Asp
ENST00000627620.2:c.615-219A>G	ENSP00000487583.1:n.615-219A>G
NM_001177984.2:c.643A>G	NP_001171455.1:p.Asn215Asp
NM_014191.3:c.643A>G	NP_055006.1:p.Asn215Asp
XM_006719556.2:c.615-219A>G	XP_006719619.1:n.615-219A>G
XM_011538650.1:c.615-219A>G	XP_011536952.1:n.615-219A>G
XM_011538651.1:c.615-219A>G	XP_011536953.1:n.615-219A>G
NM_001330260.1:c.615-219A>G	NP_001317189.1:n.615-219A>G
XM_006719556.4:c.615-219A>G	XP_006719619.1:n.615-219A>G
XM_011538651.3:c.615-219A>G	XP_011536953.1:n.615-219A>G
XM_017019794.2:c.643A>G	XP_016875283.1:p.Asn215Asp
XM_017019795.2:c.615-219A>G	XP_016875284.1:n.615-219A>G
XM_017019796.1:c.615-219A>G	XP_016875285.1:n.615-219A>G
NM_001330260.2:c.615-219A>G MANE Select	NP_001317189.1:n.615-219A>G
NM_001369788.1:c.615-219A>G	NP_001356717.1:n.615-219A>G
NM_014191.4:c.643A>G MANE Plus Clinical	NP_055006.1:p.Asn215Asp
NM_001177984.3:c.643A>G	NP_001171455.1:p.Asn215Asp