Canonical Allele Identifier: CA480062217
Gene: SCN8A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52200661C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51806877C>G , CM000674.2:g.51806877C>G GRCh38
NC_000012.11:g.52200661C>G , CM000674.1:g.52200661C>G GRCh37
NC_000012.10:g.50486928C>G NCBI36
NG_021180.2:g.220642C>G
NG_021180.3:g.221920C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000354534.11:c.5391C>G MANE Plus Clinical ENSP00000346534.4:p.Pro1797=
ENST00000627620.5:c.5391C>G MANE Select ENSP00000487583.2:p.Pro1797=
ENST00000636945.2:c.3455C>G
ENST00000662684.1:c.5391C>G ENSP00000499636.1:p.Pro1797=
ENST00000668547.1:c.5268C>G ENSP00000499691.1:p.Pro1756=
ENST00000354534.10:c.5391C>G ENSP00000346534.4:p.Pro1797=
ENST00000355133.7:c.5268C>G ENSP00000347255.4:p.Pro1756=
ENST00000545061.5:c.5268C>G ENSP00000440360.1:p.Pro1756=
ENST00000599343.5:c.5424C>G ENSP00000476447.3:p.Pro1808=
ENST00000627620.2:c.5391C>G ENSP00000487583.1:p.Pro1797=
NM_001177984.2:c.5268C>G NP_001171455.1:p.Pro1756=
NM_014191.3:c.5391C>G NP_055006.1:p.Pro1797=
XM_006719556.2:c.5391C>G XP_006719619.1:p.Pro1797=
XM_011538650.1:c.5391C>G XP_011536952.1:p.Pro1797=
XM_011538651.1:c.5391C>G XP_011536953.1:p.Pro1797=
NM_001330260.1:c.5391C>G NP_001317189.1:p.Pro1797=
XM_006719556.4:c.5391C>G XP_006719619.1:p.Pro1797=
XM_011538651.3:c.5391C>G XP_011536953.1:p.Pro1797=
XM_017019794.2:c.5391C>G XP_016875283.1:p.Pro1797=
XM_017019795.2:c.5268C>G XP_016875284.1:p.Pro1756=
NM_001330260.2:c.5391C>G MANE Select NP_001317189.1:p.Pro1797=
NM_001369788.1:c.5268C>G NP_001356717.1:p.Pro1756=
NM_014191.4:c.5391C>G MANE Plus Clinical NP_055006.1:p.Pro1797=
NM_001177984.3:c.5268C>G NP_001171455.1:p.Pro1756=
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