Canonical Allele Identifier: CA2036195206
Gene: SCN8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51807376_51807379delinsGGAA , CM000674.2:g.51807376_51807379delinsGGAA GRCh38
NC_000012.11:g.52201160_52201163delinsGGAA , CM000674.1:g.52201160_52201163delinsGGAA GRCh37
NC_000012.10:g.50487427_50487430delinsGGAA NCBI36
NG_021180.2:g.221141_221144delinsGGAA
NG_021180.3:g.222419_222422delinsGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354534.11:c.5890_5893delinsGGAA MANE Plus Clinical ENSP00000346534.4:p.Gly1964=
ENST00000627620.5:c.5890_5893delinsGGAA MANE Select ENSP00000487583.2:p.Gly1964=
ENST00000662684.1:c.5890_5893delinsGGAA ENSP00000499636.1:p.Gly1964=
ENST00000668547.1:c.5767_5770delinsGGAA ENSP00000499691.1:p.Gly1923=
ENST00000354534.10:c.5890_5893delinsGGAA ENSP00000346534.4:p.Gly1964=
ENST00000355133.7:c.5767_5770delinsGGAA ENSP00000347255.4:p.Gly1923=
ENST00000545061.5:c.5767_5770delinsGGAA ENSP00000440360.1:p.Gly1923=
ENST00000599343.5:c.5923_5926delinsGGAA ENSP00000476447.3:p.Gly1975=
ENST00000627620.2:c.5890_5893delinsGGAA ENSP00000487583.1:p.Gly1964=
NM_001177984.2:c.5767_5770delinsGGAA NP_001171455.1:p.Gly1923=
NM_014191.3:c.5890_5893delinsGGAA NP_055006.1:p.Gly1964=
XM_006719556.2:c.5890_5893delinsGGAA XP_006719619.1:p.Gly1964=
XM_011538650.1:c.5890_5893delinsGGAA XP_011536952.1:p.Gly1964=
XM_011538651.1:c.5890_5893delinsGGAA XP_011536953.1:p.Gly1964=
NM_001330260.1:c.5890_5893delinsGGAA NP_001317189.1:p.Gly1964=
XM_006719556.4:c.5890_5893delinsGGAA XP_006719619.1:p.Gly1964=
XM_011538651.3:c.5890_5893delinsGGAA XP_011536953.1:p.Gly1964=
XM_017019794.2:c.5890_5893delinsGGAA XP_016875283.1:p.Gly1964=
XM_017019795.2:c.5767_5770delinsGGAA XP_016875284.1:p.Gly1923=
NM_001330260.2:c.5890_5893delinsGGAA MANE Select NP_001317189.1:p.Gly1964=
NM_001369788.1:c.5767_5770delinsGGAA NP_001356717.1:p.Gly1923=
NM_014191.4:c.5890_5893delinsGGAA MANE Plus Clinical NP_055006.1:p.Gly1964=
NM_001177984.3:c.5767_5770delinsGGAA NP_001171455.1:p.Gly1923=