Canonical Allele Identifier: CA2618840703

Gene: SCN8A

Linked Data

• gnomAD v4: 12-51765659-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51765659_51765660insC , CM000674.2:g.51765659_51765660insC	GRCh38
NC_000012.11:g.52159443_52159444insC , CM000674.1:g.52159443_52159444insC	GRCh37
NC_000012.10:g.50445710_50445711insC	NCBI36
NG_021180.2:g.179424_179425insC
NG_021180.3:g.180702_180703insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.2545-12_2545-11insC MANE Plus Clinical	ENSP00000346534.4:n.2545-12_2545-11insC
ENST00000548086.3:c.392-12_392-11insC
ENST00000627620.5:c.2545-12_2545-11insC MANE Select	ENSP00000487583.2:n.2545-12_2545-11insC
ENST00000636945.2:c.549-12_549-11insC
ENST00000662684.1:c.2545-12_2545-11insC	ENSP00000499636.1:n.2545-12_2545-11insC
ENST00000668547.1:c.2545-12_2545-11insC	ENSP00000499691.1:n.2545-12_2545-11insC
ENST00000354534.10:c.2545-12_2545-11insC	ENSP00000346534.4:n.2545-12_2545-11insC
ENST00000355133.7:c.2545-12_2545-11insC	ENSP00000347255.4:n.2545-12_2545-11insC
ENST00000545061.5:c.2545-12_2545-11insC	ENSP00000440360.1:n.2545-12_2545-11insC
ENST00000550891.4:n.2673-12_2673-11insC
ENST00000599343.5:c.2578-12_2578-11insC	ENSP00000476447.3:n.2578-12_2578-11insC
ENST00000627620.2:c.2545-12_2545-11insC	ENSP00000487583.1:n.2545-12_2545-11insC
NM_001177984.2:c.2545-12_2545-11insC	NP_001171455.1:n.2545-12_2545-11insC
NM_014191.3:c.2545-12_2545-11insC	NP_055006.1:n.2545-12_2545-11insC
XM_006719556.2:c.2545-12_2545-11insC	XP_006719619.1:n.2545-12_2545-11insC
XM_011538650.1:c.2545-12_2545-11insC	XP_011536952.1:n.2545-12_2545-11insC
XM_011538651.1:c.2545-12_2545-11insC	XP_011536953.1:n.2545-12_2545-11insC
NM_001330260.1:c.2545-12_2545-11insC	NP_001317189.1:n.2545-12_2545-11insC
XM_006719556.4:c.2545-12_2545-11insC	XP_006719619.1:n.2545-12_2545-11insC
XM_011538651.3:c.2545-12_2545-11insC	XP_011536953.1:n.2545-12_2545-11insC
XM_017019794.2:c.2545-12_2545-11insC	XP_016875283.1:n.2545-12_2545-11insC
XM_017019795.2:c.2545-12_2545-11insC	XP_016875284.1:n.2545-12_2545-11insC
XM_017019796.1:c.2545-12_2545-11insC	XP_016875285.1:n.2545-12_2545-11insC
NM_001330260.2:c.2545-12_2545-11insC MANE Select	NP_001317189.1:n.2545-12_2545-11insC
NM_001369788.1:c.2545-12_2545-11insC	NP_001356717.1:n.2545-12_2545-11insC
NM_014191.4:c.2545-12_2545-11insC MANE Plus Clinical	NP_055006.1:n.2545-12_2545-11insC
NM_001177984.3:c.2545-12_2545-11insC	NP_001171455.1:n.2545-12_2545-11insC