Canonical Allele Identifier: CA384892238

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 641899
• ClinVar RCV Id: RCV000795246
• dbSNP Id: rs781237471
• MyVariant Identifiers: chr12:g.52162808G>T (hg19) ; chr12:g.51769024G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51769024G>T , CM000674.2:g.51769024G>T	GRCh38
NC_000012.11:g.52162808G>T , CM000674.1:g.52162808G>T	GRCh37
NC_000012.10:g.50449075G>T	NCBI36
NG_021180.2:g.182789G>T
NG_021180.3:g.184067G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.3061G>T MANE Plus Clinical	ENSP00000346534.4:p.Ala1021Ser
ENST00000548086.3:c.908G>T
ENST00000627620.5:c.3061G>T MANE Select	ENSP00000487583.2:p.Ala1021Ser
ENST00000636945.2:c.1125G>T
ENST00000662684.1:c.3061G>T	ENSP00000499636.1:p.Ala1021Ser
ENST00000668547.1:c.3061G>T	ENSP00000499691.1:p.Ala1021Ser
ENST00000354534.10:c.3061G>T	ENSP00000346534.4:p.Ala1021Ser
ENST00000355133.7:c.3061G>T	ENSP00000347255.4:p.Ala1021Ser
ENST00000545061.5:c.3061G>T	ENSP00000440360.1:p.Ala1021Ser
ENST00000599343.5:c.3094G>T	ENSP00000476447.3:p.Ala1032Ser
ENST00000627620.2:c.3061G>T	ENSP00000487583.1:p.Ala1021Ser
ENST00000627665.1:n.53G>T
NM_001177984.2:c.3061G>T	NP_001171455.1:p.Ala1021Ser
NM_014191.3:c.3061G>T	NP_055006.1:p.Ala1021Ser
XM_006719556.2:c.3061G>T	XP_006719619.1:p.Ala1021Ser
XM_011538650.1:c.3061G>T	XP_011536952.1:p.Ala1021Ser
XM_011538651.1:c.3061G>T	XP_011536953.1:p.Ala1021Ser
NM_001330260.1:c.3061G>T	NP_001317189.1:p.Ala1021Ser
XM_006719556.4:c.3061G>T	XP_006719619.1:p.Ala1021Ser
XM_011538651.3:c.3061G>T	XP_011536953.1:p.Ala1021Ser
XM_017019794.2:c.3061G>T	XP_016875283.1:p.Ala1021Ser
XM_017019795.2:c.3061G>T	XP_016875284.1:p.Ala1021Ser
XM_017019796.1:c.3061G>T	XP_016875285.1:p.Ala1021Ser
NM_001330260.2:c.3061G>T MANE Select	NP_001317189.1:p.Ala1021Ser
NM_001369788.1:c.3061G>T	NP_001356717.1:p.Ala1021Ser
NM_014191.4:c.3061G>T MANE Plus Clinical	NP_055006.1:p.Ala1021Ser
NM_001177984.3:c.3061G>T	NP_001171455.1:p.Ala1021Ser