Canonical Allele Identifier: CA384880251
Gene: SCN8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51806281G>C , CM000674.2:g.51806281G>C GRCh38
NC_000012.11:g.52200065G>C , CM000674.1:g.52200065G>C GRCh37
NC_000012.10:g.50486332G>C NCBI36
NG_021180.2:g.220046G>C
NG_021180.3:g.221324G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354534.11:c.4796-1G>C MANE Plus Clinical ENSP00000346534.4:n.4796-1G>C
ENST00000627620.5:c.4796-1G>C MANE Select ENSP00000487583.2:n.4796-1G>C
ENST00000636945.2:c.2860-1G>C
ENST00000662684.1:c.4796-1G>C ENSP00000499636.1:n.4796-1G>C
ENST00000668547.1:c.4673-1G>C ENSP00000499691.1:n.4673-1G>C
ENST00000354534.10:c.4796-1G>C ENSP00000346534.4:n.4796-1G>C
ENST00000355133.7:c.4673-1G>C ENSP00000347255.4:n.4673-1G>C
ENST00000545061.5:c.4673-1G>C ENSP00000440360.1:n.4673-1G>C
ENST00000599343.5:c.4829-1G>C ENSP00000476447.3:n.4829-1G>C
ENST00000627620.2:c.4796-1G>C ENSP00000487583.1:n.4796-1G>C
NM_001177984.2:c.4673-1G>C NP_001171455.1:n.4673-1G>C
NM_014191.3:c.4796-1G>C NP_055006.1:n.4796-1G>C
XM_006719556.2:c.4796-1G>C XP_006719619.1:n.4796-1G>C
XM_011538650.1:c.4796-1G>C XP_011536952.1:n.4796-1G>C
XM_011538651.1:c.4796-1G>C XP_011536953.1:n.4796-1G>C
NM_001330260.1:c.4796-1G>C NP_001317189.1:n.4796-1G>C
XM_006719556.4:c.4796-1G>C XP_006719619.1:n.4796-1G>C
XM_011538651.3:c.4796-1G>C XP_011536953.1:n.4796-1G>C
XM_017019794.2:c.4796-1G>C XP_016875283.1:n.4796-1G>C
XM_017019795.2:c.4673-1G>C XP_016875284.1:n.4673-1G>C
NM_001330260.2:c.4796-1G>C MANE Select NP_001317189.1:n.4796-1G>C
NM_001369788.1:c.4673-1G>C NP_001356717.1:n.4673-1G>C
NM_014191.4:c.4796-1G>C MANE Plus Clinical NP_055006.1:n.4796-1G>C
NM_001177984.3:c.4673-1G>C NP_001171455.1:n.4673-1G>C