Canonical Allele Identifier: CA303505
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189995
ClinVar RCV Id: RCV000180951

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165998040_165999778del , CM000664.2:g.165998040_165999778del GRCh38
NC_000002.11:g.166854550_166856288del , CM000664.1:g.166854550_166856288del GRCh37
NC_000002.10:g.166562796_166564534del NCBI36
NG_011906.1:g.78864_80602del , LRG_8:g.78864_80602del

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*2321_*2512del
ENST00000303395.9:c.4285_4476del
ENST00000635750.1:c.4252_4443del
ENST00000635776.1:c.4252_4443del
ENST00000636194.1:c.*1778_*1969del
ENST00000637038.1:c.1147_1338del
ENST00000637988.1:c.4252_4443del
ENST00000640036.1:c.4252_4443del
ENST00000641575.1:c.4249_4440del
ENST00000641603.1:c.4003_4194del
ENST00000641996.1:c.*3839_*4030del
ENST00000671940.1:c.*2228_*2419del
ENST00000673490.1:n.6758_6949del
ENST00000674923.1:c.4285_4476del
ENST00000303395.8:c.4285_4476del
ENST00000375405.7:c.4252_4443del
ENST00000409050.1:c.4201_4392del
ENST00000423058.6:c.4285_4476del
ENST00000473295.2:n.288_479del
NM_001165963.1:c.4285_4476del
NM_001165964.1:c.4201_4392del
NM_001202435.1:c.4285_4476del
NM_006920.4:c.4252_4443del , LRG_8t1:c.4252_4443del
NR_110598.1:n.176-17573_176-15835del
XM_011511598.1:c.4285_4476del
XM_011511599.1:c.4285_4476del
XM_011511600.1:c.4285_4476del
XM_011511601.1:c.4285_4476del
XM_011511602.1:c.4285_4476del
XM_011511603.1:c.4282_4473del
XM_011511604.1:c.4252_4443del
XM_011511605.1:c.4249_4440del
XM_011511606.1:c.4201_4392del
XM_011511607.1:c.4003_4194del
NM_001165963.2:c.4285_4476del
NM_001165964.2:c.4201_4392del
NM_001202435.2:c.4285_4476del
NM_001353948.1:c.4285_4476del
NM_001353949.1:c.4252_4443del
NM_001353950.1:c.4252_4443del
NM_001353951.1:c.4252_4443del
NM_001353952.1:c.4252_4443del
NM_001353954.1:c.4249_4440del
NM_001353955.1:c.4249_4440del
NM_001353957.1:c.4201_4392del
NM_001353958.1:c.4201_4392del
NM_001353960.1:c.4198_4389del
NM_001353961.1:c.1843_2034del
NM_006920.5:c.4252_4443del
NR_148667.1:n.4721_4912del
XR_001738883.1:n.4735_4926del
XR_001738884.1:n.4707_4898del
NM_001165963.3:c.4285_4476del
NM_001165964.3:c.4201_4392del
NM_001202435.3:c.4285_4476del
NM_001353948.2:c.4285_4476del
NM_001353949.2:c.4252_4443del
NM_001353950.2:c.4252_4443del
NM_001353951.2:c.4252_4443del
NM_001353952.2:c.4252_4443del
NM_001353954.2:c.4249_4440del
NM_001353955.2:c.4249_4440del
NM_001353957.2:c.4201_4392del
NM_001353958.2:c.4201_4392del
NM_001353960.2:c.4198_4389del
NM_001353961.2:c.1843_2034del
NM_006920.6:c.4252_4443del
NR_148667.2:n.4702_4893del
NM_001165963.4:c.4285_4476del