Canonical Allele Identifier: CA2618841116

Gene: SCN8A

Linked Data

• gnomAD v4: 12-51769474-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51769477del , CM000674.2:g.51769477del	GRCh38
NC_000012.11:g.52163261del , CM000674.1:g.52163261del	GRCh37
NC_000012.10:g.50449528del	NCBI36
NG_021180.2:g.183242del
NG_021180.3:g.184520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.3372+142del MANE Plus Clinical	ENSP00000346534.4:n.3372+142del
ENST00000548086.3:c.1219+142del
ENST00000627620.5:c.3372+142del MANE Select	ENSP00000487583.2:n.3372+142del
ENST00000636945.2:c.1436+142del
ENST00000662684.1:c.3372+142del	ENSP00000499636.1:n.3372+142del
ENST00000668547.1:c.3372+142del	ENSP00000499691.1:n.3372+142del
ENST00000354534.10:c.3372+142del	ENSP00000346534.4:n.3372+142del
ENST00000355133.7:c.3372+142del	ENSP00000347255.4:n.3372+142del
ENST00000545061.5:c.3372+142del	ENSP00000440360.1:n.3372+142del
ENST00000599343.5:c.3405+142del	ENSP00000476447.3:n.3405+142del
ENST00000627620.2:c.3372+142del	ENSP00000487583.1:n.3372+142del
ENST00000627665.1:n.364+142del
NM_001177984.2:c.3372+142del	NP_001171455.1:n.3372+142del
NM_014191.3:c.3372+142del	NP_055006.1:n.3372+142del
XM_006719556.2:c.3372+142del	XP_006719619.1:n.3372+142del
XM_011538650.1:c.3372+142del	XP_011536952.1:n.3372+142del
XM_011538651.1:c.3372+142del	XP_011536953.1:n.3372+142del
NM_001330260.1:c.3372+142del	NP_001317189.1:n.3372+142del
XM_006719556.4:c.3372+142del	XP_006719619.1:n.3372+142del
XM_011538651.3:c.3372+142del	XP_011536953.1:n.3372+142del
XM_017019794.2:c.3372+142del	XP_016875283.1:n.3372+142del
XM_017019795.2:c.3372+142del	XP_016875284.1:n.3372+142del
XM_017019796.1:c.3372+142del	XP_016875285.1:n.3372+142del
NM_001330260.2:c.3372+142del MANE Select	NP_001317189.1:n.3372+142del
NM_001369788.1:c.3372+142del	NP_001356717.1:n.3372+142del
NM_014191.4:c.3372+142del MANE Plus Clinical	NP_055006.1:n.3372+142del
NM_001177984.3:c.3372+142del	NP_001171455.1:n.3372+142del