Canonical Allele Identifier: CA947681498
Gene: SCN8A HGNC NCBI

Linked Data

dbSNP Id: rs1942825924

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51765614_51765616del , CM000674.2:g.51765614_51765616del GRCh38
NC_000012.11:g.52159398_52159400del , CM000674.1:g.52159398_52159400del GRCh37
NC_000012.10:g.50445665_50445667del NCBI36
NG_021180.2:g.179379_179381del
NG_021180.3:g.180657_180659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354534.11:c.2545-57_2545-55del MANE Plus Clinical ENSP00000346534.4:n.2545-57_2545-55del
ENST00000548086.3:c.392-57_392-55del
ENST00000627620.5:c.2545-57_2545-55del MANE Select ENSP00000487583.2:n.2545-57_2545-55del
ENST00000636945.2:c.549-57_549-55del
ENST00000662684.1:c.2545-57_2545-55del ENSP00000499636.1:n.2545-57_2545-55del
ENST00000668547.1:c.2545-57_2545-55del ENSP00000499691.1:n.2545-57_2545-55del
ENST00000354534.10:c.2545-57_2545-55del ENSP00000346534.4:n.2545-57_2545-55del
ENST00000355133.7:c.2545-57_2545-55del ENSP00000347255.4:n.2545-57_2545-55del
ENST00000545061.5:c.2545-57_2545-55del ENSP00000440360.1:n.2545-57_2545-55del
ENST00000550891.4:n.2673-57_2673-55del
ENST00000599343.5:c.2578-57_2578-55del ENSP00000476447.3:n.2578-57_2578-55del
ENST00000627620.2:c.2545-57_2545-55del ENSP00000487583.1:n.2545-57_2545-55del
NM_001177984.2:c.2545-57_2545-55del NP_001171455.1:n.2545-57_2545-55del
NM_014191.3:c.2545-57_2545-55del NP_055006.1:n.2545-57_2545-55del
XM_006719556.2:c.2545-57_2545-55del XP_006719619.1:n.2545-57_2545-55del
XM_011538650.1:c.2545-57_2545-55del XP_011536952.1:n.2545-57_2545-55del
XM_011538651.1:c.2545-57_2545-55del XP_011536953.1:n.2545-57_2545-55del
NM_001330260.1:c.2545-57_2545-55del NP_001317189.1:n.2545-57_2545-55del
XM_006719556.4:c.2545-57_2545-55del XP_006719619.1:n.2545-57_2545-55del
XM_011538651.3:c.2545-57_2545-55del XP_011536953.1:n.2545-57_2545-55del
XM_017019794.2:c.2545-57_2545-55del XP_016875283.1:n.2545-57_2545-55del
XM_017019795.2:c.2545-57_2545-55del XP_016875284.1:n.2545-57_2545-55del
XM_017019796.1:c.2545-57_2545-55del XP_016875285.1:n.2545-57_2545-55del
NM_001330260.2:c.2545-57_2545-55del MANE Select NP_001317189.1:n.2545-57_2545-55del
NM_001369788.1:c.2545-57_2545-55del NP_001356717.1:n.2545-57_2545-55del
NM_014191.4:c.2545-57_2545-55del MANE Plus Clinical NP_055006.1:n.2545-57_2545-55del
NM_001177984.3:c.2545-57_2545-55del NP_001171455.1:n.2545-57_2545-55del