Canonical Allele Identifier: CA1304837641

Gene: SCN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165991940_165991941delinsTC , CM000664.2:g.165991940_165991941delinsTC	GRCh38
NC_000002.11:g.166848450_166848451delinsTC , CM000664.1:g.166848450_166848451delinsTC	GRCh37
NC_000002.10:g.166556696_166556697delinsTC	NCBI36
NG_011906.1:g.86699_86700delinsGA , LRG_8:g.86699_86700delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000689288.1:c.*3370_*3371delinsGA	ENSP00000509637.1:n.*3370_*3371delinsGA
ENST00000303395.9:c.5334_5335delinsGA	ENSP00000303540.4:p.Val1778=
ENST00000635750.1:c.5301_5302delinsGA	ENSP00000490799.1:p.Val1767=
ENST00000635776.1:c.*2167_*2168delinsGA	ENSP00000490692.1:n.*2167_*2168delinsGA
ENST00000636194.1:c.*2827_*2828delinsGA	ENSP00000490288.1:n.*2827_*2828delinsGA
ENST00000637038.1:c.2196_2197delinsGA
ENST00000637988.1:c.5301_5302delinsGA	ENSP00000490780.1:p.Val1767=
ENST00000640036.1:c.5301_5302delinsGA	ENSP00000491573.1:p.Val1767=
ENST00000641575.1:c.5298_5299delinsGA	ENSP00000492917.1:p.Val1766=
ENST00000641603.1:c.5052_5053delinsGA	ENSP00000492945.1:p.Val1684=
ENST00000641996.1:c.*4888_*4889delinsGA	ENSP00000493054.1:n.*4888_*4889delinsGA
ENST00000671940.1:c.*3277_*3278delinsGA	ENSP00000500336.1:n.*3277_*3278delinsGA
ENST00000673490.1:n.7807_7808delinsGA
ENST00000674923.1:c.5334_5335delinsGA MANE Select	ENSP00000501589.1:p.Val1778=
ENST00000303395.8:c.5334_5335delinsGA	ENSP00000303540.4:p.Val1778=
ENST00000375405.7:c.5301_5302delinsGA	ENSP00000364554.3:p.Val1767=
ENST00000409050.1:c.5250_5251delinsGA	ENSP00000386312.1:p.Val1750=
ENST00000423058.6:c.5334_5335delinsGA	ENSP00000407030.2:p.Val1778=
NM_001165963.1:c.5334_5335delinsGA	NP_001159435.1:p.Val1778=
NM_001165964.1:c.5250_5251delinsGA	NP_001159436.1:p.Val1750=
NM_001202435.1:c.5334_5335delinsGA	NP_001189364.1:p.Val1778=
NM_006920.4:c.5301_5302delinsGA , LRG_8t1:c.5301_5302delinsGA	NP_008851.3:p.Val1767=
NR_110598.1:n.176-23673_176-23672delinsTC
XM_011511598.1:c.5334_5335delinsGA	XP_011509900.1:p.Val1778=
XM_011511599.1:c.5334_5335delinsGA	XP_011509901.1:p.Val1778=
XM_011511600.1:c.5334_5335delinsGA	XP_011509902.1:p.Val1778=
XM_011511601.1:c.5334_5335delinsGA	XP_011509903.1:p.Val1778=
XM_011511602.1:c.5334_5335delinsGA	XP_011509904.1:p.Val1778=
XM_011511603.1:c.5331_5332delinsGA	XP_011509905.1:p.Val1777=
XM_011511604.1:c.5301_5302delinsGA	XP_011509906.1:p.Val1767=
XM_011511605.1:c.5298_5299delinsGA	XP_011509907.1:p.Val1766=
XM_011511606.1:c.5250_5251delinsGA	XP_011509908.1:p.Val1750=
XM_011511607.1:c.5052_5053delinsGA	XP_011509909.1:p.Val1684=
NM_001165963.2:c.5334_5335delinsGA	NP_001159435.1:p.Val1778=
NM_001165964.2:c.5250_5251delinsGA	NP_001159436.1:p.Val1750=
NM_001202435.2:c.5334_5335delinsGA	NP_001189364.1:p.Val1778=
NM_001353948.1:c.5334_5335delinsGA	NP_001340877.1:p.Val1778=
NM_001353949.1:c.5301_5302delinsGA	NP_001340878.1:p.Val1767=
NM_001353950.1:c.5301_5302delinsGA	NP_001340879.1:p.Val1767=
NM_001353951.1:c.5301_5302delinsGA	NP_001340880.1:p.Val1767=
NM_001353952.1:c.5301_5302delinsGA	NP_001340881.1:p.Val1767=
NM_001353954.1:c.5298_5299delinsGA	NP_001340883.1:p.Val1766=
NM_001353955.1:c.5298_5299delinsGA	NP_001340884.1:p.Val1766=
NM_001353957.1:c.5250_5251delinsGA	NP_001340886.1:p.Val1750=
NM_001353958.1:c.5250_5251delinsGA	NP_001340887.1:p.Val1750=
NM_001353960.1:c.5247_5248delinsGA	NP_001340889.1:p.Val1749=
NM_001353961.1:c.2892_2893delinsGA	NP_001340890.1:p.Val964=
NM_006920.5:c.5301_5302delinsGA	NP_008851.3:p.Val1767=
NR_148667.1:n.5770_5771delinsGA
XR_001738883.1:n.5784_5785delinsGA
XR_001738884.1:n.5756_5757delinsGA
NM_001165963.3:c.5334_5335delinsGA	NP_001159435.1:p.Val1778=
NM_001165964.3:c.5250_5251delinsGA	NP_001159436.1:p.Val1750=
NM_001202435.3:c.5334_5335delinsGA	NP_001189364.1:p.Val1778=
NM_001353948.2:c.5334_5335delinsGA	NP_001340877.1:p.Val1778=
NM_001353949.2:c.5301_5302delinsGA	NP_001340878.1:p.Val1767=
NM_001353950.2:c.5301_5302delinsGA	NP_001340879.1:p.Val1767=
NM_001353951.2:c.5301_5302delinsGA	NP_001340880.1:p.Val1767=
NM_001353952.2:c.5301_5302delinsGA	NP_001340881.1:p.Val1767=
NM_001353954.2:c.5298_5299delinsGA	NP_001340883.1:p.Val1766=
NM_001353955.2:c.5298_5299delinsGA	NP_001340884.1:p.Val1766=
NM_001353957.2:c.5250_5251delinsGA	NP_001340886.1:p.Val1750=
NM_001353958.2:c.5250_5251delinsGA	NP_001340887.1:p.Val1750=
NM_001353960.2:c.5247_5248delinsGA	NP_001340889.1:p.Val1749=
NM_001353961.2:c.2892_2893delinsGA	NP_001340890.1:p.Val964=
NM_006920.6:c.5301_5302delinsGA	NP_008851.3:p.Val1767=
NR_148667.2:n.5751_5752delinsGA
NM_001165963.4:c.5334_5335delinsGA MANE Select	NP_001159435.1:p.Val1778=