Canonical Allele Identifier: CA1304837601
Gene: SCN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165991931T= , CM000664.2:g.165991931T= GRCh38
NC_000002.11:g.166848441T= , CM000664.1:g.166848441T= GRCh37
NC_000002.10:g.166556687T= NCBI36
NG_011906.1:g.86709A= , LRG_8:g.86709A=

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*3380A= ENSP00000509637.1:n.*3380A=
ENST00000303395.9:c.5344A= ENSP00000303540.4:p.Ile1782=
ENST00000635750.1:c.5311A= ENSP00000490799.1:p.Ile1771=
ENST00000635776.1:c.*2177A= ENSP00000490692.1:n.*2177A=
ENST00000636194.1:c.*2837A= ENSP00000490288.1:n.*2837A=
ENST00000637038.1:c.2206A=
ENST00000637988.1:c.5311A= ENSP00000490780.1:p.Ile1771=
ENST00000640036.1:c.5311A= ENSP00000491573.1:p.Ile1771=
ENST00000641575.1:c.5308A= ENSP00000492917.1:p.Ile1770=
ENST00000641603.1:c.5062A= ENSP00000492945.1:p.Ile1688=
ENST00000641996.1:c.*4898A= ENSP00000493054.1:n.*4898A=
ENST00000671940.1:c.*3287A= ENSP00000500336.1:n.*3287A=
ENST00000673490.1:n.7817A=
ENST00000674923.1:c.5344A= MANE Select ENSP00000501589.1:p.Ile1782=
ENST00000303395.8:c.5344A= ENSP00000303540.4:p.Ile1782=
ENST00000375405.7:c.5311A= ENSP00000364554.3:p.Ile1771=
ENST00000409050.1:c.5260A= ENSP00000386312.1:p.Ile1754=
ENST00000423058.6:c.5344A= ENSP00000407030.2:p.Ile1782=
NM_001165963.1:c.5344A= NP_001159435.1:p.Ile1782=
NM_001165964.1:c.5260A= NP_001159436.1:p.Ile1754=
NM_001202435.1:c.5344A= NP_001189364.1:p.Ile1782=
NM_006920.4:c.5311A= , LRG_8t1:c.5311A= NP_008851.3:p.Ile1771=
NR_110598.1:n.176-23682T=
XM_011511598.1:c.5344A= XP_011509900.1:p.Ile1782=
XM_011511599.1:c.5344A= XP_011509901.1:p.Ile1782=
XM_011511600.1:c.5344A= XP_011509902.1:p.Ile1782=
XM_011511601.1:c.5344A= XP_011509903.1:p.Ile1782=
XM_011511602.1:c.5344A= XP_011509904.1:p.Ile1782=
XM_011511603.1:c.5341A= XP_011509905.1:p.Ile1781=
XM_011511604.1:c.5311A= XP_011509906.1:p.Ile1771=
XM_011511605.1:c.5308A= XP_011509907.1:p.Ile1770=
XM_011511606.1:c.5260A= XP_011509908.1:p.Ile1754=
XM_011511607.1:c.5062A= XP_011509909.1:p.Ile1688=
NM_001165963.2:c.5344A= NP_001159435.1:p.Ile1782=
NM_001165964.2:c.5260A= NP_001159436.1:p.Ile1754=
NM_001202435.2:c.5344A= NP_001189364.1:p.Ile1782=
NM_001353948.1:c.5344A= NP_001340877.1:p.Ile1782=
NM_001353949.1:c.5311A= NP_001340878.1:p.Ile1771=
NM_001353950.1:c.5311A= NP_001340879.1:p.Ile1771=
NM_001353951.1:c.5311A= NP_001340880.1:p.Ile1771=
NM_001353952.1:c.5311A= NP_001340881.1:p.Ile1771=
NM_001353954.1:c.5308A= NP_001340883.1:p.Ile1770=
NM_001353955.1:c.5308A= NP_001340884.1:p.Ile1770=
NM_001353957.1:c.5260A= NP_001340886.1:p.Ile1754=
NM_001353958.1:c.5260A= NP_001340887.1:p.Ile1754=
NM_001353960.1:c.5257A= NP_001340889.1:p.Ile1753=
NM_001353961.1:c.2902A= NP_001340890.1:p.Ile968=
NM_006920.5:c.5311A= NP_008851.3:p.Ile1771=
NR_148667.1:n.5780A=
XR_001738883.1:n.5794A=
XR_001738884.1:n.5766A=
NM_001165963.3:c.5344A= NP_001159435.1:p.Ile1782=
NM_001165964.3:c.5260A= NP_001159436.1:p.Ile1754=
NM_001202435.3:c.5344A= NP_001189364.1:p.Ile1782=
NM_001353948.2:c.5344A= NP_001340877.1:p.Ile1782=
NM_001353949.2:c.5311A= NP_001340878.1:p.Ile1771=
NM_001353950.2:c.5311A= NP_001340879.1:p.Ile1771=
NM_001353951.2:c.5311A= NP_001340880.1:p.Ile1771=
NM_001353952.2:c.5311A= NP_001340881.1:p.Ile1771=
NM_001353954.2:c.5308A= NP_001340883.1:p.Ile1770=
NM_001353955.2:c.5308A= NP_001340884.1:p.Ile1770=
NM_001353957.2:c.5260A= NP_001340886.1:p.Ile1754=
NM_001353958.2:c.5260A= NP_001340887.1:p.Ile1754=
NM_001353960.2:c.5257A= NP_001340889.1:p.Ile1753=
NM_001353961.2:c.2902A= NP_001340890.1:p.Ile968=
NM_006920.6:c.5311A= NP_008851.3:p.Ile1771=
NR_148667.2:n.5761A=
NM_001165963.4:c.5344A= MANE Select NP_001159435.1:p.Ile1782=