Canonical Allele Identifier: CA2618840735

Gene: SCN8A

Linked Data

• gnomAD v4: 12-51786411-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51786411C>T , CM000674.2:g.51786411C>T	GRCh38
NC_000012.11:g.52180195C>T , CM000674.1:g.52180195C>T	GRCh37
NC_000012.10:g.50466462C>T	NCBI36
NG_021180.2:g.200176C>T
NG_021180.3:g.201454C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354534.11:c.3943-131C>T MANE Plus Clinical	ENSP00000346534.4:n.3943-131C>T
ENST00000548086.3:c.1737-131C>T
ENST00000627620.5:c.3943-131C>T MANE Select	ENSP00000487583.2:n.3943-131C>T
ENST00000636945.2:c.2007-131C>T
ENST00000662684.1:c.3943-131C>T	ENSP00000499636.1:n.3943-131C>T
ENST00000668547.1:c.3820-131C>T	ENSP00000499691.1:n.3820-131C>T
ENST00000354534.10:c.3943-131C>T	ENSP00000346534.4:n.3943-131C>T
ENST00000355133.7:c.3820-131C>T	ENSP00000347255.4:n.3820-131C>T
ENST00000545061.5:c.3820-131C>T	ENSP00000440360.1:n.3820-131C>T
ENST00000548086.1:n.194-131C>T
ENST00000599343.5:c.3976-131C>T	ENSP00000476447.3:n.3976-131C>T
ENST00000627620.2:c.3943-131C>T	ENSP00000487583.1:n.3943-131C>T
NM_001177984.2:c.3820-131C>T	NP_001171455.1:n.3820-131C>T
NM_014191.3:c.3943-131C>T	NP_055006.1:n.3943-131C>T
XM_006719556.2:c.3943-131C>T	XP_006719619.1:n.3943-131C>T
XM_011538650.1:c.3943-131C>T	XP_011536952.1:n.3943-131C>T
XM_011538651.1:c.3943-131C>T	XP_011536953.1:n.3943-131C>T
NM_001330260.1:c.3943-131C>T	NP_001317189.1:n.3943-131C>T
XM_006719556.4:c.3943-131C>T	XP_006719619.1:n.3943-131C>T
XM_011538651.3:c.3943-131C>T	XP_011536953.1:n.3943-131C>T
XM_017019794.2:c.3943-131C>T	XP_016875283.1:n.3943-131C>T
XM_017019795.2:c.3820-131C>T	XP_016875284.1:n.3820-131C>T
XM_017019796.1:c.*41-131C>T	XP_016875285.1:n.*41-131C>T
NM_001330260.2:c.3943-131C>T MANE Select	NP_001317189.1:n.3943-131C>T
NM_001369788.1:c.3820-131C>T	NP_001356717.1:n.3820-131C>T
NM_014191.4:c.3943-131C>T MANE Plus Clinical	NP_055006.1:n.3943-131C>T
NM_001177984.3:c.3820-131C>T	NP_001171455.1:n.3820-131C>T