Canonical Allele Identifier: CA480062383
Gene: SCN8A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52200724T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51806940T>A , CM000674.2:g.51806940T>A GRCh38
NC_000012.11:g.52200724T>A , CM000674.1:g.52200724T>A GRCh37
NC_000012.10:g.50486991T>A NCBI36
NG_021180.2:g.220705T>A
NG_021180.3:g.221983T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354534.11:c.5454T>A MANE Plus Clinical ENSP00000346534.4:p.Pro1818=
ENST00000627620.5:c.5454T>A MANE Select ENSP00000487583.2:p.Pro1818=
ENST00000636945.2:c.3518T>A
ENST00000662684.1:c.5454T>A ENSP00000499636.1:p.Pro1818=
ENST00000668547.1:c.5331T>A ENSP00000499691.1:p.Pro1777=
ENST00000354534.10:c.5454T>A ENSP00000346534.4:p.Pro1818=
ENST00000355133.7:c.5331T>A ENSP00000347255.4:p.Pro1777=
ENST00000545061.5:c.5331T>A ENSP00000440360.1:p.Pro1777=
ENST00000599343.5:c.5487T>A ENSP00000476447.3:p.Pro1829=
ENST00000627620.2:c.5454T>A ENSP00000487583.1:p.Pro1818=
NM_001177984.2:c.5331T>A NP_001171455.1:p.Pro1777=
NM_014191.3:c.5454T>A NP_055006.1:p.Pro1818=
XM_006719556.2:c.5454T>A XP_006719619.1:p.Pro1818=
XM_011538650.1:c.5454T>A XP_011536952.1:p.Pro1818=
XM_011538651.1:c.5454T>A XP_011536953.1:p.Pro1818=
NM_001330260.1:c.5454T>A NP_001317189.1:p.Pro1818=
XM_006719556.4:c.5454T>A XP_006719619.1:p.Pro1818=
XM_011538651.3:c.5454T>A XP_011536953.1:p.Pro1818=
XM_017019794.2:c.5454T>A XP_016875283.1:p.Pro1818=
XM_017019795.2:c.5331T>A XP_016875284.1:p.Pro1777=
NM_001330260.2:c.5454T>A MANE Select NP_001317189.1:p.Pro1818=
NM_001369788.1:c.5331T>A NP_001356717.1:p.Pro1777=
NM_014191.4:c.5454T>A MANE Plus Clinical NP_055006.1:p.Pro1818=
NM_001177984.3:c.5331T>A NP_001171455.1:p.Pro1777=
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