Canonical Allele Identifier: CA2586970327
Gene: SCN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166002489_166002490del , CM000664.2:g.166002489_166002490del GRCh38
NC_000002.11:g.166858999_166859000del , CM000664.1:g.166858999_166859000del GRCh37
NC_000002.10:g.166567245_166567246del NCBI36
NG_011906.1:g.76155_76156del , LRG_8:g.76155_76156del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689288.1:c.*2307_*2308del ENSP00000509637.1:n.*2307_*2308del
ENST00000303395.9:c.4271_4272del ENSP00000303540.4:p.Ser1424PhefsTer19
ENST00000635750.1:c.4238_4239del ENSP00000490799.1:p.Ser1413PhefsTer19
ENST00000635776.1:c.4238_4239del ENSP00000490692.1:p.Ser1413PhefsTer19
ENST00000636194.1:c.*1764_*1765del ENSP00000490288.1:n.*1764_*1765del
ENST00000637038.1:c.1133_1134del
ENST00000637988.1:c.4238_4239del ENSP00000490780.1:p.Ser1413PhefsTer19
ENST00000640036.1:c.4238_4239del ENSP00000491573.1:p.Ser1413PhefsTer19
ENST00000641575.1:c.4235_4236del ENSP00000492917.1:p.Ser1412PhefsTer19
ENST00000641603.1:c.4003-2709_4003-2708del ENSP00000492945.1:n.4003-2709_4003-2708del
ENST00000641996.1:c.*3825_*3826del ENSP00000493054.1:n.*3825_*3826del
ENST00000671940.1:c.*2214_*2215del ENSP00000500336.1:n.*2214_*2215del
ENST00000673490.1:n.6744_6745del
ENST00000674923.1:c.4271_4272del MANE Select ENSP00000501589.1:p.Ser1424PhefsTer19
ENST00000303395.8:c.4271_4272del ENSP00000303540.4:p.Ser1424PhefsTer19
ENST00000375405.7:c.4238_4239del ENSP00000364554.3:p.Ser1413PhefsTer19
ENST00000409050.1:c.4187_4188del ENSP00000386312.1:p.Ser1396PhefsTer19
ENST00000423058.6:c.4271_4272del ENSP00000407030.2:p.Ser1424PhefsTer19
ENST00000491429.1:n.424_425del
NM_001165963.1:c.4271_4272del NP_001159435.1:p.Ser1424PhefsTer19
NM_001165964.1:c.4187_4188del NP_001159436.1:p.Ser1396PhefsTer19
NM_001202435.1:c.4271_4272del NP_001189364.1:p.Ser1424PhefsTer19
NM_006920.4:c.4238_4239del , LRG_8t1:c.4238_4239del NP_008851.3:p.Ser1413PhefsTer19
NR_110598.1:n.176-13124_176-13123del
XM_011511598.1:c.4271_4272del XP_011509900.1:p.Ser1424PhefsTer19
XM_011511599.1:c.4271_4272del XP_011509901.1:p.Ser1424PhefsTer19
XM_011511600.1:c.4271_4272del XP_011509902.1:p.Ser1424PhefsTer19
XM_011511601.1:c.4271_4272del XP_011509903.1:p.Ser1424PhefsTer19
XM_011511602.1:c.4271_4272del XP_011509904.1:p.Ser1424PhefsTer19
XM_011511603.1:c.4268_4269del XP_011509905.1:p.Ser1423PhefsTer19
XM_011511604.1:c.4238_4239del XP_011509906.1:p.Ser1413PhefsTer19
XM_011511605.1:c.4235_4236del XP_011509907.1:p.Ser1412PhefsTer19
XM_011511606.1:c.4187_4188del XP_011509908.1:p.Ser1396PhefsTer19
XM_011511607.1:c.4003-2709_4003-2708del XP_011509909.1:n.4003-2709_4003-2708del
XR_922981.1:n.4519_4520del
NM_001165963.2:c.4271_4272del NP_001159435.1:p.Ser1424PhefsTer19
NM_001165964.2:c.4187_4188del NP_001159436.1:p.Ser1396PhefsTer19
NM_001202435.2:c.4271_4272del NP_001189364.1:p.Ser1424PhefsTer19
NM_001353948.1:c.4271_4272del NP_001340877.1:p.Ser1424PhefsTer19
NM_001353949.1:c.4238_4239del NP_001340878.1:p.Ser1413PhefsTer19
NM_001353950.1:c.4238_4239del NP_001340879.1:p.Ser1413PhefsTer19
NM_001353951.1:c.4238_4239del NP_001340880.1:p.Ser1413PhefsTer19
NM_001353952.1:c.4238_4239del NP_001340881.1:p.Ser1413PhefsTer19
NM_001353954.1:c.4235_4236del NP_001340883.1:p.Ser1412PhefsTer19
NM_001353955.1:c.4235_4236del NP_001340884.1:p.Ser1412PhefsTer19
NM_001353957.1:c.4187_4188del NP_001340886.1:p.Ser1396PhefsTer19
NM_001353958.1:c.4187_4188del NP_001340887.1:p.Ser1396PhefsTer19
NM_001353960.1:c.4184_4185del NP_001340889.1:p.Ser1395PhefsTer19
NM_001353961.1:c.1829_1830del NP_001340890.1:p.Ser610PhefsTer19
NM_006920.5:c.4238_4239del NP_008851.3:p.Ser1413PhefsTer19
NR_148667.1:n.4707_4708del
XR_001738883.1:n.4721_4722del
XR_001738884.1:n.4693_4694del
NM_001165963.3:c.4271_4272del NP_001159435.1:p.Ser1424PhefsTer19
NM_001165964.3:c.4187_4188del NP_001159436.1:p.Ser1396PhefsTer19
NM_001202435.3:c.4271_4272del NP_001189364.1:p.Ser1424PhefsTer19
NM_001353948.2:c.4271_4272del NP_001340877.1:p.Ser1424PhefsTer19
NM_001353949.2:c.4238_4239del NP_001340878.1:p.Ser1413PhefsTer19
NM_001353950.2:c.4238_4239del NP_001340879.1:p.Ser1413PhefsTer19
NM_001353951.2:c.4238_4239del NP_001340880.1:p.Ser1413PhefsTer19
NM_001353952.2:c.4238_4239del NP_001340881.1:p.Ser1413PhefsTer19
NM_001353954.2:c.4235_4236del NP_001340883.1:p.Ser1412PhefsTer19
NM_001353955.2:c.4235_4236del NP_001340884.1:p.Ser1412PhefsTer19
NM_001353957.2:c.4187_4188del NP_001340886.1:p.Ser1396PhefsTer19
NM_001353958.2:c.4187_4188del NP_001340887.1:p.Ser1396PhefsTer19
NM_001353960.2:c.4184_4185del NP_001340889.1:p.Ser1395PhefsTer19
NM_001353961.2:c.1829_1830del NP_001340890.1:p.Ser610PhefsTer19
NM_006920.6:c.4238_4239del NP_008851.3:p.Ser1413PhefsTer19
NR_148667.2:n.4688_4689del
NM_001165963.4:c.4271_4272del MANE Select NP_001159435.1:p.Ser1424PhefsTer19