Canonical Allele Identifier: CA2036196391

Gene: SCN8A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51751612_51751613delinsTC , CM000674.2:g.51751612_51751613delinsTC	GRCh38
NC_000012.11:g.52145396_52145397delinsTC , CM000674.1:g.52145396_52145397delinsTC	GRCh37
NC_000012.10:g.50431663_50431664delinsTC	NCBI36
NG_021180.2:g.165377_165378delinsTC
NG_021180.3:g.166655_166656delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354534.11:c.2370+19_2370+20delinsTC MANE Plus Clinical	ENSP00000346534.4:n.2370+19_2370+20delinsTC
ENST00000548086.3:c.217+19_217+20delinsTC
ENST00000627620.5:c.2370+19_2370+20delinsTC MANE Select	ENSP00000487583.2:n.2370+19_2370+20delinsTC
ENST00000636945.2:c.374+19_374+20delinsTC
ENST00000662684.1:c.2370+19_2370+20delinsTC	ENSP00000499636.1:n.2370+19_2370+20delinsTC
ENST00000668547.1:c.2370+19_2370+20delinsTC	ENSP00000499691.1:n.2370+19_2370+20delinsTC
ENST00000354534.10:c.2370+19_2370+20delinsTC	ENSP00000346534.4:n.2370+19_2370+20delinsTC
ENST00000355133.7:c.2370+19_2370+20delinsTC	ENSP00000347255.4:n.2370+19_2370+20delinsTC
ENST00000545061.5:c.2370+19_2370+20delinsTC	ENSP00000440360.1:n.2370+19_2370+20delinsTC
ENST00000550891.4:n.2498+19_2498+20delinsTC
ENST00000599343.5:c.2403+19_2403+20delinsTC	ENSP00000476447.3:n.2403+19_2403+20delinsTC
ENST00000627620.2:c.2370+19_2370+20delinsTC	ENSP00000487583.1:n.2370+19_2370+20delinsTC
NM_001177984.2:c.2370+19_2370+20delinsTC	NP_001171455.1:n.2370+19_2370+20delinsTC
NM_014191.3:c.2370+19_2370+20delinsTC	NP_055006.1:n.2370+19_2370+20delinsTC
XM_006719556.2:c.2370+19_2370+20delinsTC	XP_006719619.1:n.2370+19_2370+20delinsTC
XM_011538650.1:c.2370+19_2370+20delinsTC	XP_011536952.1:n.2370+19_2370+20delinsTC
XM_011538651.1:c.2370+19_2370+20delinsTC	XP_011536953.1:n.2370+19_2370+20delinsTC
NM_001330260.1:c.2370+19_2370+20delinsTC	NP_001317189.1:n.2370+19_2370+20delinsTC
XM_006719556.4:c.2370+19_2370+20delinsTC	XP_006719619.1:n.2370+19_2370+20delinsTC
XM_011538651.3:c.2370+19_2370+20delinsTC	XP_011536953.1:n.2370+19_2370+20delinsTC
XM_017019794.2:c.2370+19_2370+20delinsTC	XP_016875283.1:n.2370+19_2370+20delinsTC
XM_017019795.2:c.2370+19_2370+20delinsTC	XP_016875284.1:n.2370+19_2370+20delinsTC
XM_017019796.1:c.2370+19_2370+20delinsTC	XP_016875285.1:n.2370+19_2370+20delinsTC
NM_001330260.2:c.2370+19_2370+20delinsTC MANE Select	NP_001317189.1:n.2370+19_2370+20delinsTC
NM_001369788.1:c.2370+19_2370+20delinsTC	NP_001356717.1:n.2370+19_2370+20delinsTC
NM_014191.4:c.2370+19_2370+20delinsTC MANE Plus Clinical	NP_055006.1:n.2370+19_2370+20delinsTC
NM_001177984.3:c.2370+19_2370+20delinsTC	NP_001171455.1:n.2370+19_2370+20delinsTC