Canonical Allele Identifier: CA236309244

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 2174959
• ClinVar RCV Id: RCV002602206
• dbSNP Id: rs932949364
• gnomAD v2: 12-52139693-A-G
• gnomAD v4: 12-51745909-A-G
• MyVariant Identifiers: chr12:g.52139693A>G (hg19) ; chr12:g.51745909A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51745909A>G , CM000674.2:g.51745909A>G	GRCh38
NC_000012.11:g.52139693A>G , CM000674.1:g.52139693A>G	GRCh37
NC_000012.10:g.50425960A>G	NCBI36
NG_021180.2:g.159674A>G
NG_021180.3:g.160952A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354534.11:c.2005A>G MANE Plus Clinical	ENSP00000346534.4:p.Thr669Ala
ENST00000627620.5:c.2005A>G MANE Select	ENSP00000487583.2:p.Thr669Ala
ENST00000636945.2:c.9A>G
ENST00000662684.1:c.2005A>G	ENSP00000499636.1:p.Thr669Ala
ENST00000668547.1:c.2005A>G	ENSP00000499691.1:p.Thr669Ala
ENST00000354534.10:c.2005A>G	ENSP00000346534.4:p.Thr669Ala
ENST00000355133.7:c.2005A>G	ENSP00000347255.4:p.Thr669Ala
ENST00000545061.5:c.2005A>G	ENSP00000440360.1:p.Thr669Ala
ENST00000550891.4:n.2133A>G
ENST00000551216.2:c.1588A>G	ENSP00000447567.2:p.Thr530Ala
ENST00000599343.5:c.2038A>G	ENSP00000476447.3:p.Thr680Ala
ENST00000627620.2:c.2005A>G	ENSP00000487583.1:p.Thr669Ala
NM_001177984.2:c.2005A>G	NP_001171455.1:p.Thr669Ala
NM_014191.3:c.2005A>G	NP_055006.1:p.Thr669Ala
XM_006719556.2:c.2005A>G	XP_006719619.1:p.Thr669Ala
XM_011538650.1:c.2005A>G	XP_011536952.1:p.Thr669Ala
XM_011538651.1:c.2005A>G	XP_011536953.1:p.Thr669Ala
NM_001330260.1:c.2005A>G	NP_001317189.1:p.Thr669Ala
XM_006719556.4:c.2005A>G	XP_006719619.1:p.Thr669Ala
XM_011538651.3:c.2005A>G	XP_011536953.1:p.Thr669Ala
XM_017019794.2:c.2005A>G	XP_016875283.1:p.Thr669Ala
XM_017019795.2:c.2005A>G	XP_016875284.1:p.Thr669Ala
XM_017019796.1:c.2005A>G	XP_016875285.1:p.Thr669Ala
NM_001330260.2:c.2005A>G MANE Select	NP_001317189.1:p.Thr669Ala
NM_001369788.1:c.2005A>G	NP_001356717.1:p.Thr669Ala
NM_014191.4:c.2005A>G MANE Plus Clinical	NP_055006.1:p.Thr669Ala
NM_001177984.3:c.2005A>G	NP_001171455.1:p.Thr669Ala