Canonical Allele Identifier: CA1304836396
Gene: SCN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165991493G= , CM000664.2:g.165991493G= GRCh38
NC_000002.11:g.166848003G= , CM000664.1:g.166848003G= GRCh37
NC_000002.10:g.166556249G= NCBI36
NG_011906.1:g.87147C= , LRG_8:g.87147C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689288.1:c.*3818C= ENSP00000509637.1:n.*3818C=
ENST00000303395.9:c.5782C= ENSP00000303540.4:p.Arg1928=
ENST00000635750.1:c.5749C= ENSP00000490799.1:p.Arg1917=
ENST00000635776.1:c.*2615C= ENSP00000490692.1:n.*2615C=
ENST00000636194.1:c.*3275C= ENSP00000490288.1:n.*3275C=
ENST00000637038.1:c.2644C=
ENST00000637988.1:c.5749C= ENSP00000490780.1:p.Arg1917=
ENST00000640036.1:c.5749C= ENSP00000491573.1:p.Arg1917=
ENST00000641575.1:c.5746C= ENSP00000492917.1:p.Arg1916=
ENST00000641603.1:c.5500C= ENSP00000492945.1:p.Arg1834=
ENST00000641996.1:c.*5336C= ENSP00000493054.1:n.*5336C=
ENST00000671940.1:c.*3725C= ENSP00000500336.1:n.*3725C=
ENST00000673490.1:n.8255C=
ENST00000674923.1:c.5782C= MANE Select ENSP00000501589.1:p.Arg1928=
ENST00000303395.8:c.5782C= ENSP00000303540.4:p.Arg1928=
ENST00000375405.7:c.5749C= ENSP00000364554.3:p.Arg1917=
ENST00000409050.1:c.5698C= ENSP00000386312.1:p.Arg1900=
ENST00000423058.6:c.5782C= ENSP00000407030.2:p.Arg1928=
NM_001165963.1:c.5782C= NP_001159435.1:p.Arg1928=
NM_001165964.1:c.5698C= NP_001159436.1:p.Arg1900=
NM_001202435.1:c.5782C= NP_001189364.1:p.Arg1928=
NM_006920.4:c.5749C= , LRG_8t1:c.5749C= NP_008851.3:p.Arg1917=
NR_110598.1:n.176-24120G=
XM_011511598.1:c.5782C= XP_011509900.1:p.Arg1928=
XM_011511599.1:c.5782C= XP_011509901.1:p.Arg1928=
XM_011511600.1:c.5782C= XP_011509902.1:p.Arg1928=
XM_011511601.1:c.5782C= XP_011509903.1:p.Arg1928=
XM_011511602.1:c.5782C= XP_011509904.1:p.Arg1928=
XM_011511603.1:c.5779C= XP_011509905.1:p.Arg1927=
XM_011511604.1:c.5749C= XP_011509906.1:p.Arg1917=
XM_011511605.1:c.5746C= XP_011509907.1:p.Arg1916=
XM_011511606.1:c.5698C= XP_011509908.1:p.Arg1900=
XM_011511607.1:c.5500C= XP_011509909.1:p.Arg1834=
NM_001165963.2:c.5782C= NP_001159435.1:p.Arg1928=
NM_001165964.2:c.5698C= NP_001159436.1:p.Arg1900=
NM_001202435.2:c.5782C= NP_001189364.1:p.Arg1928=
NM_001353948.1:c.5782C= NP_001340877.1:p.Arg1928=
NM_001353949.1:c.5749C= NP_001340878.1:p.Arg1917=
NM_001353950.1:c.5749C= NP_001340879.1:p.Arg1917=
NM_001353951.1:c.5749C= NP_001340880.1:p.Arg1917=
NM_001353952.1:c.5749C= NP_001340881.1:p.Arg1917=
NM_001353954.1:c.5746C= NP_001340883.1:p.Arg1916=
NM_001353955.1:c.5746C= NP_001340884.1:p.Arg1916=
NM_001353957.1:c.5698C= NP_001340886.1:p.Arg1900=
NM_001353958.1:c.5698C= NP_001340887.1:p.Arg1900=
NM_001353960.1:c.5695C= NP_001340889.1:p.Arg1899=
NM_001353961.1:c.3340C= NP_001340890.1:p.Arg1114=
NM_006920.5:c.5749C= NP_008851.3:p.Arg1917=
NR_148667.1:n.6218C=
XR_001738883.1:n.6232C=
XR_001738884.1:n.6204C=
NM_001165963.3:c.5782C= NP_001159435.1:p.Arg1928=
NM_001165964.3:c.5698C= NP_001159436.1:p.Arg1900=
NM_001202435.3:c.5782C= NP_001189364.1:p.Arg1928=
NM_001353948.2:c.5782C= NP_001340877.1:p.Arg1928=
NM_001353949.2:c.5749C= NP_001340878.1:p.Arg1917=
NM_001353950.2:c.5749C= NP_001340879.1:p.Arg1917=
NM_001353951.2:c.5749C= NP_001340880.1:p.Arg1917=
NM_001353952.2:c.5749C= NP_001340881.1:p.Arg1917=
NM_001353954.2:c.5746C= NP_001340883.1:p.Arg1916=
NM_001353955.2:c.5746C= NP_001340884.1:p.Arg1916=
NM_001353957.2:c.5698C= NP_001340886.1:p.Arg1900=
NM_001353958.2:c.5698C= NP_001340887.1:p.Arg1900=
NM_001353960.2:c.5695C= NP_001340889.1:p.Arg1899=
NM_001353961.2:c.3340C= NP_001340890.1:p.Arg1114=
NM_006920.6:c.5749C= NP_008851.3:p.Arg1917=
NR_148667.2:n.6199C=
NM_001165963.4:c.5782C= MANE Select NP_001159435.1:p.Arg1928=