Canonical Allele Identifier: CA2036192815

Gene: SCN8A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51806351C= , CM000674.2:g.51806351C=	GRCh38
NC_000012.11:g.52200135C= , CM000674.1:g.52200135C=	GRCh37
NC_000012.10:g.50486402C=	NCBI36
NG_021180.2:g.220116C=
NG_021180.3:g.221394C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354534.11:c.4865C= MANE Plus Clinical	ENSP00000346534.4:p.Ala1622=
ENST00000627620.5:c.4865C= MANE Select	ENSP00000487583.2:p.Ala1622=
ENST00000636945.2:c.2929C=
ENST00000662684.1:c.4865C=	ENSP00000499636.1:p.Ala1622=
ENST00000668547.1:c.4742C=	ENSP00000499691.1:p.Ala1581=
ENST00000354534.10:c.4865C=	ENSP00000346534.4:p.Ala1622=
ENST00000355133.7:c.4742C=	ENSP00000347255.4:p.Ala1581=
ENST00000545061.5:c.4742C=	ENSP00000440360.1:p.Ala1581=
ENST00000599343.5:c.4898C=	ENSP00000476447.3:p.Ala1633=
ENST00000627620.2:c.4865C=	ENSP00000487583.1:p.Ala1622=
NM_001177984.2:c.4742C=	NP_001171455.1:p.Ala1581=
NM_014191.3:c.4865C=	NP_055006.1:p.Ala1622=
XM_006719556.2:c.4865C=	XP_006719619.1:p.Ala1622=
XM_011538650.1:c.4865C=	XP_011536952.1:p.Ala1622=
XM_011538651.1:c.4865C=	XP_011536953.1:p.Ala1622=
NM_001330260.1:c.4865C=	NP_001317189.1:p.Ala1622=
XM_006719556.4:c.4865C=	XP_006719619.1:p.Ala1622=
XM_011538651.3:c.4865C=	XP_011536953.1:p.Ala1622=
XM_017019794.2:c.4865C=	XP_016875283.1:p.Ala1622=
XM_017019795.2:c.4742C=	XP_016875284.1:p.Ala1581=
NM_001330260.2:c.4865C= MANE Select	NP_001317189.1:p.Ala1622=
NM_001369788.1:c.4742C=	NP_001356717.1:p.Ala1581=
NM_014191.4:c.4865C= MANE Plus Clinical	NP_055006.1:p.Ala1622=
NM_001177984.3:c.4742C=	NP_001171455.1:p.Ala1581=