Canonical Allele Identifier: CA2661760152
Gene: SCN1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166002437_166002438del , CM000664.2:g.166002437_166002438del GRCh38
NC_000002.11:g.166858947_166858948del , CM000664.1:g.166858947_166858948del GRCh37
NC_000002.10:g.166567193_166567194del NCBI36
NG_011906.1:g.76202_76203del , LRG_8:g.76202_76203del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689288.1:c.*2320+34_*2320+35del ENSP00000509637.1:n.*2320+34_*2320+35del
ENST00000303395.9:c.4284+34_4284+35del ENSP00000303540.4:n.4284+34_4284+35del
ENST00000635750.1:c.4251+34_4251+35del ENSP00000490799.1:n.4251+34_4251+35del
ENST00000635776.1:c.4251+34_4251+35del ENSP00000490692.1:n.4251+34_4251+35del
ENST00000635893.1:c.15+34_15+35del ENSP00000489986.1:n.15+34_15+35del
ENST00000636194.1:c.*1777+34_*1777+35del ENSP00000490288.1:n.*1777+34_*1777+35del
ENST00000637038.1:c.1146+34_1146+35del
ENST00000637988.1:c.4251+34_4251+35del ENSP00000490780.1:n.4251+34_4251+35del
ENST00000640036.1:c.4251+34_4251+35del ENSP00000491573.1:n.4251+34_4251+35del
ENST00000641575.1:c.4248+34_4248+35del ENSP00000492917.1:n.4248+34_4248+35del
ENST00000641603.1:c.4003-2662_4003-2661del ENSP00000492945.1:n.4003-2662_4003-2661del
ENST00000641996.1:c.*3838+34_*3838+35del ENSP00000493054.1:n.*3838+34_*3838+35del
ENST00000671940.1:c.*2227+34_*2227+35del ENSP00000500336.1:n.*2227+34_*2227+35del
ENST00000673490.1:n.6757+34_6757+35del
ENST00000674923.1:c.4284+34_4284+35del MANE Select ENSP00000501589.1:n.4284+34_4284+35del
ENST00000303395.8:c.4284+34_4284+35del ENSP00000303540.4:n.4284+34_4284+35del
ENST00000375405.7:c.4251+34_4251+35del ENSP00000364554.3:n.4251+34_4251+35del
ENST00000409050.1:c.4200+34_4200+35del ENSP00000386312.1:n.4200+34_4200+35del
ENST00000423058.6:c.4284+34_4284+35del ENSP00000407030.2:n.4284+34_4284+35del
ENST00000491429.1:n.437+34_437+35del
NM_001165963.1:c.4284+34_4284+35del NP_001159435.1:n.4284+34_4284+35del
NM_001165964.1:c.4200+34_4200+35del NP_001159436.1:n.4200+34_4200+35del
NM_001202435.1:c.4284+34_4284+35del NP_001189364.1:n.4284+34_4284+35del
NM_006920.4:c.4251+34_4251+35del , LRG_8t1:c.4251+34_4251+35del NP_008851.3:n.4251+34_4251+35del
NR_110598.1:n.176-13176_176-13175del
XM_011511598.1:c.4284+34_4284+35del XP_011509900.1:n.4284+34_4284+35del
XM_011511599.1:c.4284+34_4284+35del XP_011509901.1:n.4284+34_4284+35del
XM_011511600.1:c.4284+34_4284+35del XP_011509902.1:n.4284+34_4284+35del
XM_011511601.1:c.4284+34_4284+35del XP_011509903.1:n.4284+34_4284+35del
XM_011511602.1:c.4284+34_4284+35del XP_011509904.1:n.4284+34_4284+35del
XM_011511603.1:c.4281+34_4281+35del XP_011509905.1:n.4281+34_4281+35del
XM_011511604.1:c.4251+34_4251+35del XP_011509906.1:n.4251+34_4251+35del
XM_011511605.1:c.4248+34_4248+35del XP_011509907.1:n.4248+34_4248+35del
XM_011511606.1:c.4200+34_4200+35del XP_011509908.1:n.4200+34_4200+35del
XM_011511607.1:c.4003-2662_4003-2661del XP_011509909.1:n.4003-2662_4003-2661del
XR_922981.1:n.4532+34_4532+35del
NM_001165963.2:c.4284+34_4284+35del NP_001159435.1:n.4284+34_4284+35del
NM_001165964.2:c.4200+34_4200+35del NP_001159436.1:n.4200+34_4200+35del
NM_001202435.2:c.4284+34_4284+35del NP_001189364.1:n.4284+34_4284+35del
NM_001353948.1:c.4284+34_4284+35del NP_001340877.1:n.4284+34_4284+35del
NM_001353949.1:c.4251+34_4251+35del NP_001340878.1:n.4251+34_4251+35del
NM_001353950.1:c.4251+34_4251+35del NP_001340879.1:n.4251+34_4251+35del
NM_001353951.1:c.4251+34_4251+35del NP_001340880.1:n.4251+34_4251+35del
NM_001353952.1:c.4251+34_4251+35del NP_001340881.1:n.4251+34_4251+35del
NM_001353954.1:c.4248+34_4248+35del NP_001340883.1:n.4248+34_4248+35del
NM_001353955.1:c.4248+34_4248+35del NP_001340884.1:n.4248+34_4248+35del
NM_001353957.1:c.4200+34_4200+35del NP_001340886.1:n.4200+34_4200+35del
NM_001353958.1:c.4200+34_4200+35del NP_001340887.1:n.4200+34_4200+35del
NM_001353960.1:c.4197+34_4197+35del NP_001340889.1:n.4197+34_4197+35del
NM_001353961.1:c.1842+34_1842+35del NP_001340890.1:n.1842+34_1842+35del
NM_006920.5:c.4251+34_4251+35del NP_008851.3:n.4251+34_4251+35del
NR_148667.1:n.4720+34_4720+35del
XR_001738883.1:n.4734+34_4734+35del
XR_001738884.1:n.4706+34_4706+35del
NM_001165963.3:c.4284+34_4284+35del NP_001159435.1:n.4284+34_4284+35del
NM_001165964.3:c.4200+34_4200+35del NP_001159436.1:n.4200+34_4200+35del
NM_001202435.3:c.4284+34_4284+35del NP_001189364.1:n.4284+34_4284+35del
NM_001353948.2:c.4284+34_4284+35del NP_001340877.1:n.4284+34_4284+35del
NM_001353949.2:c.4251+34_4251+35del NP_001340878.1:n.4251+34_4251+35del
NM_001353950.2:c.4251+34_4251+35del NP_001340879.1:n.4251+34_4251+35del
NM_001353951.2:c.4251+34_4251+35del NP_001340880.1:n.4251+34_4251+35del
NM_001353952.2:c.4251+34_4251+35del NP_001340881.1:n.4251+34_4251+35del
NM_001353954.2:c.4248+34_4248+35del NP_001340883.1:n.4248+34_4248+35del
NM_001353955.2:c.4248+34_4248+35del NP_001340884.1:n.4248+34_4248+35del
NM_001353957.2:c.4200+34_4200+35del NP_001340886.1:n.4200+34_4200+35del
NM_001353958.2:c.4200+34_4200+35del NP_001340887.1:n.4200+34_4200+35del
NM_001353960.2:c.4197+34_4197+35del NP_001340889.1:n.4197+34_4197+35del
NM_001353961.2:c.1842+34_1842+35del NP_001340890.1:n.1842+34_1842+35del
NM_006920.6:c.4251+34_4251+35del NP_008851.3:n.4251+34_4251+35del
NR_148667.2:n.4701+34_4701+35del
NM_001165963.4:c.4284+34_4284+35del MANE Select NP_001159435.1:n.4284+34_4284+35del