Canonical Allele Identifier: CA6571922

Gene: SCN8A

Linked Data

• ClinVar Variation Id: 579919
• ClinVar RCV Id: RCV000703318 ; RCV000763861 ; RCV002343547
• dbSNP Id: rs764115258
• ExAC: 12:52200749 A / G
• gnomAD v2: 12-52200749-A-G
• gnomAD v3: 12-51806965-A-G
• gnomAD v4: 12-51806965-A-G
• MyVariant Identifiers: chr12:g.52200749A>G (hg19) ; chr12:g.51806965A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51806965A>G , CM000674.2:g.51806965A>G	GRCh38
NC_000012.11:g.52200749A>G , CM000674.1:g.52200749A>G	GRCh37
NC_000012.10:g.50487016A>G	NCBI36
NG_021180.2:g.220730A>G
NG_021180.3:g.222008A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.5479A>G MANE Plus Clinical	ENSP00000346534.4:p.Ile1827Val
ENST00000627620.5:c.5479A>G MANE Select	ENSP00000487583.2:p.Ile1827Val
ENST00000636945.2:c.3543A>G
ENST00000662684.1:c.5479A>G	ENSP00000499636.1:p.Ile1827Val
ENST00000668547.1:c.5356A>G	ENSP00000499691.1:p.Ile1786Val
ENST00000354534.10:c.5479A>G	ENSP00000346534.4:p.Ile1827Val
ENST00000355133.7:c.5356A>G	ENSP00000347255.4:p.Ile1786Val
ENST00000545061.5:c.5356A>G	ENSP00000440360.1:p.Ile1786Val
ENST00000599343.5:c.5512A>G	ENSP00000476447.3:p.Ile1838Val
ENST00000627620.2:c.5479A>G	ENSP00000487583.1:p.Ile1827Val
NM_001177984.2:c.5356A>G	NP_001171455.1:p.Ile1786Val
NM_014191.3:c.5479A>G	NP_055006.1:p.Ile1827Val
XM_006719556.2:c.5479A>G	XP_006719619.1:p.Ile1827Val
XM_011538650.1:c.5479A>G	XP_011536952.1:p.Ile1827Val
XM_011538651.1:c.5479A>G	XP_011536953.1:p.Ile1827Val
NM_001330260.1:c.5479A>G	NP_001317189.1:p.Ile1827Val
XM_006719556.4:c.5479A>G	XP_006719619.1:p.Ile1827Val
XM_011538651.3:c.5479A>G	XP_011536953.1:p.Ile1827Val
XM_017019794.2:c.5479A>G	XP_016875283.1:p.Ile1827Val
XM_017019795.2:c.5356A>G	XP_016875284.1:p.Ile1786Val
NM_001330260.2:c.5479A>G MANE Select	NP_001317189.1:p.Ile1827Val
NM_001369788.1:c.5356A>G	NP_001356717.1:p.Ile1786Val
NM_014191.4:c.5479A>G MANE Plus Clinical	NP_055006.1:p.Ile1827Val
NM_001177984.3:c.5356A>G	NP_001171455.1:p.Ile1786Val