Canonical Allele Identifier: CA2586970319
Gene: SCN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165999774_165999776del , CM000664.2:g.165999774_165999776del GRCh38
NC_000002.11:g.166856284_166856286del , CM000664.1:g.166856284_166856286del GRCh37
NC_000002.10:g.166564530_166564532del NCBI36
NG_011906.1:g.78864_78866del , LRG_8:g.78864_78866del

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*2321_*2323del ENSP00000509637.1:n.*2321_*2323del
ENST00000303395.9:c.4285_4287del ENSP00000303540.4:p.Ala1429del
ENST00000635750.1:c.4252_4254del ENSP00000490799.1:p.Ala1418del
ENST00000635776.1:c.4252_4254del ENSP00000490692.1:p.Ala1418del
ENST00000635893.1:c.16_18del ENSP00000489986.1:p.Ala6del
ENST00000636194.1:c.*1778_*1780del ENSP00000490288.1:n.*1778_*1780del
ENST00000637038.1:c.1147_1149del
ENST00000637988.1:c.4252_4254del ENSP00000490780.1:p.Ala1418del
ENST00000640036.1:c.4252_4254del ENSP00000491573.1:p.Ala1418del
ENST00000641575.1:c.4249_4251del ENSP00000492917.1:p.Ala1417del
ENST00000641603.1:c.4003_4005del ENSP00000492945.1:p.Ala1335del
ENST00000641996.1:c.*3839_*3841del ENSP00000493054.1:n.*3839_*3841del
ENST00000671940.1:c.*2228_*2230del ENSP00000500336.1:n.*2228_*2230del
ENST00000673490.1:n.6758_6760del
ENST00000674923.1:c.4285_4287del MANE Select ENSP00000501589.1:p.Ala1429del
ENST00000303395.8:c.4285_4287del ENSP00000303540.4:p.Ala1429del
ENST00000375405.7:c.4252_4254del ENSP00000364554.3:p.Ala1418del
ENST00000409050.1:c.4201_4203del ENSP00000386312.1:p.Ala1401del
ENST00000423058.6:c.4285_4287del ENSP00000407030.2:p.Ala1429del
ENST00000473295.2:n.288_290del
ENST00000491429.1:n.438_440del
NM_001165963.1:c.4285_4287del NP_001159435.1:p.Ala1429del
NM_001165964.1:c.4201_4203del NP_001159436.1:p.Ala1401del
NM_001202435.1:c.4285_4287del NP_001189364.1:p.Ala1429del
NM_006920.4:c.4252_4254del , LRG_8t1:c.4252_4254del NP_008851.3:p.Ala1418del
NR_110598.1:n.176-15839_176-15837del
XM_011511598.1:c.4285_4287del XP_011509900.1:p.Ala1429del
XM_011511599.1:c.4285_4287del XP_011509901.1:p.Ala1429del
XM_011511600.1:c.4285_4287del XP_011509902.1:p.Ala1429del
XM_011511601.1:c.4285_4287del XP_011509903.1:p.Ala1429del
XM_011511602.1:c.4285_4287del XP_011509904.1:p.Ala1429del
XM_011511603.1:c.4282_4284del XP_011509905.1:p.Ala1428del
XM_011511604.1:c.4252_4254del XP_011509906.1:p.Ala1418del
XM_011511605.1:c.4249_4251del XP_011509907.1:p.Ala1417del
XM_011511606.1:c.4201_4203del XP_011509908.1:p.Ala1401del
XM_011511607.1:c.4003_4005del XP_011509909.1:p.Ala1335del
XR_922981.1:n.4533_4535del
NM_001165963.2:c.4285_4287del NP_001159435.1:p.Ala1429del
NM_001165964.2:c.4201_4203del NP_001159436.1:p.Ala1401del
NM_001202435.2:c.4285_4287del NP_001189364.1:p.Ala1429del
NM_001353948.1:c.4285_4287del NP_001340877.1:p.Ala1429del
NM_001353949.1:c.4252_4254del NP_001340878.1:p.Ala1418del
NM_001353950.1:c.4252_4254del NP_001340879.1:p.Ala1418del
NM_001353951.1:c.4252_4254del NP_001340880.1:p.Ala1418del
NM_001353952.1:c.4252_4254del NP_001340881.1:p.Ala1418del
NM_001353954.1:c.4249_4251del NP_001340883.1:p.Ala1417del
NM_001353955.1:c.4249_4251del NP_001340884.1:p.Ala1417del
NM_001353957.1:c.4201_4203del NP_001340886.1:p.Ala1401del
NM_001353958.1:c.4201_4203del NP_001340887.1:p.Ala1401del
NM_001353960.1:c.4198_4200del NP_001340889.1:p.Ala1400del
NM_001353961.1:c.1843_1845del NP_001340890.1:p.Ala615del
NM_006920.5:c.4252_4254del NP_008851.3:p.Ala1418del
NR_148667.1:n.4721_4723del
XR_001738883.1:n.4735_4737del
XR_001738884.1:n.4707_4709del
NM_001165963.3:c.4285_4287del NP_001159435.1:p.Ala1429del
NM_001165964.3:c.4201_4203del NP_001159436.1:p.Ala1401del
NM_001202435.3:c.4285_4287del NP_001189364.1:p.Ala1429del
NM_001353948.2:c.4285_4287del NP_001340877.1:p.Ala1429del
NM_001353949.2:c.4252_4254del NP_001340878.1:p.Ala1418del
NM_001353950.2:c.4252_4254del NP_001340879.1:p.Ala1418del
NM_001353951.2:c.4252_4254del NP_001340880.1:p.Ala1418del
NM_001353952.2:c.4252_4254del NP_001340881.1:p.Ala1418del
NM_001353954.2:c.4249_4251del NP_001340883.1:p.Ala1417del
NM_001353955.2:c.4249_4251del NP_001340884.1:p.Ala1417del
NM_001353957.2:c.4201_4203del NP_001340886.1:p.Ala1401del
NM_001353958.2:c.4201_4203del NP_001340887.1:p.Ala1401del
NM_001353960.2:c.4198_4200del NP_001340889.1:p.Ala1400del
NM_001353961.2:c.1843_1845del NP_001340890.1:p.Ala615del
NM_006920.6:c.4252_4254del NP_008851.3:p.Ala1418del
NR_148667.2:n.4702_4704del
NM_001165963.4:c.4285_4287del MANE Select NP_001159435.1:p.Ala1429del