Canonical Allele Identifier: CA2036165086

Gene: SCN8A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51702595T= , CM000674.2:g.51702595T=	GRCh38
NC_000012.11:g.52096379T= , CM000674.1:g.52096379T=	GRCh37
NC_000012.10:g.50382646T=	NCBI36
NG_021180.2:g.116360T=
NG_021180.3:g.117638T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.993-178T= MANE Plus Clinical	ENSP00000346534.4:n.993-178T=
ENST00000627620.5:c.993-178T= MANE Select	ENSP00000487583.2:n.993-178T=
ENST00000637709.2:c.*1431-178T=	ENSP00000490470.1:n.*1431-178T=
ENST00000638820.1:c.993-178T=	ENSP00000492157.1:n.993-178T=
ENST00000662684.1:c.993-178T=	ENSP00000499636.1:n.993-178T=
ENST00000667214.1:c.993-178T=	ENSP00000499724.1:n.993-178T=
ENST00000668547.1:c.993-178T=	ENSP00000499691.1:n.993-178T=
ENST00000354534.10:c.993-178T=	ENSP00000346534.4:n.993-178T=
ENST00000355133.7:c.993-178T=	ENSP00000347255.4:n.993-178T=
ENST00000545061.5:c.993-178T=	ENSP00000440360.1:n.993-178T=
ENST00000550891.4:n.1121-178T=
ENST00000551216.2:c.543-178T=	ENSP00000447567.2:n.543-178T=
ENST00000599343.5:c.993-178T=	ENSP00000476447.3:n.993-178T=
ENST00000627620.2:c.993-178T=	ENSP00000487583.1:n.993-178T=
NM_001177984.2:c.993-178T=	NP_001171455.1:n.993-178T=
NM_014191.3:c.993-178T=	NP_055006.1:n.993-178T=
XM_006719556.2:c.993-178T=	XP_006719619.1:n.993-178T=
XM_011538650.1:c.993-178T=	XP_011536952.1:n.993-178T=
XM_011538651.1:c.993-178T=	XP_011536953.1:n.993-178T=
NM_001330260.1:c.993-178T=	NP_001317189.1:n.993-178T=
XM_006719556.4:c.993-178T=	XP_006719619.1:n.993-178T=
XM_011538651.3:c.993-178T=	XP_011536953.1:n.993-178T=
XM_017019794.2:c.993-178T=	XP_016875283.1:n.993-178T=
XM_017019795.2:c.993-178T=	XP_016875284.1:n.993-178T=
XM_017019796.1:c.993-178T=	XP_016875285.1:n.993-178T=
NM_001330260.2:c.993-178T= MANE Select	NP_001317189.1:n.993-178T=
NM_001369788.1:c.993-178T=	NP_001356717.1:n.993-178T=
NM_014191.4:c.993-178T= MANE Plus Clinical	NP_055006.1:n.993-178T=
NM_001177984.3:c.993-178T=	NP_001171455.1:n.993-178T=