Canonical Allele Identifier: CA384882164

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 2772241
• ClinVar RCV Id: RCV003591088
• MyVariant Identifiers: chr12:g.52200251G>A (hg19) ; chr12:g.51806467G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51806467G>A , CM000674.2:g.51806467G>A	GRCh38
NC_000012.11:g.52200251G>A , CM000674.1:g.52200251G>A	GRCh37
NC_000012.10:g.50486518G>A	NCBI36
NG_021180.2:g.220232G>A
NG_021180.3:g.221510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.4981G>A MANE Plus Clinical	ENSP00000346534.4:p.Val1661Ile
ENST00000627620.5:c.4981G>A MANE Select	ENSP00000487583.2:p.Val1661Ile
ENST00000636945.2:c.3045G>A
ENST00000662684.1:c.4981G>A	ENSP00000499636.1:p.Val1661Ile
ENST00000668547.1:c.4858G>A	ENSP00000499691.1:p.Val1620Ile
ENST00000354534.10:c.4981G>A	ENSP00000346534.4:p.Val1661Ile
ENST00000355133.7:c.4858G>A	ENSP00000347255.4:p.Val1620Ile
ENST00000545061.5:c.4858G>A	ENSP00000440360.1:p.Val1620Ile
ENST00000599343.5:c.5014G>A	ENSP00000476447.3:p.Val1672Ile
ENST00000627620.2:c.4981G>A	ENSP00000487583.1:p.Val1661Ile
NM_001177984.2:c.4858G>A	NP_001171455.1:p.Val1620Ile
NM_014191.3:c.4981G>A	NP_055006.1:p.Val1661Ile
XM_006719556.2:c.4981G>A	XP_006719619.1:p.Val1661Ile
XM_011538650.1:c.4981G>A	XP_011536952.1:p.Val1661Ile
XM_011538651.1:c.4981G>A	XP_011536953.1:p.Val1661Ile
NM_001330260.1:c.4981G>A	NP_001317189.1:p.Val1661Ile
XM_006719556.4:c.4981G>A	XP_006719619.1:p.Val1661Ile
XM_011538651.3:c.4981G>A	XP_011536953.1:p.Val1661Ile
XM_017019794.2:c.4981G>A	XP_016875283.1:p.Val1661Ile
XM_017019795.2:c.4858G>A	XP_016875284.1:p.Val1620Ile
NM_001330260.2:c.4981G>A MANE Select	NP_001317189.1:p.Val1661Ile
NM_001369788.1:c.4858G>A	NP_001356717.1:p.Val1620Ile
NM_014191.4:c.4981G>A MANE Plus Clinical	NP_055006.1:p.Val1661Ile
NM_001177984.3:c.4858G>A	NP_001171455.1:p.Val1620Ile