Canonical Allele Identifier: CA317743
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206925
ClinVar RCV Id: RCV000189069
dbSNP Id: rs796053087

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165991530del , CM000664.2:g.165991530del GRCh38
NC_000002.11:g.166848040del , CM000664.1:g.166848040del GRCh37
NC_000002.10:g.166556286del NCBI36
NG_011906.1:g.87111del , LRG_8:g.87111del

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*3782del ENSP00000509637.1:n.*3782del
ENST00000303395.9:c.5746del ENSP00000303540.4:p.Glu1916LysfsTer16
ENST00000635750.1:c.5713del ENSP00000490799.1:p.Glu1905LysfsTer16
ENST00000635776.1:c.*2579del ENSP00000490692.1:n.*2579del
ENST00000636194.1:c.*3239del ENSP00000490288.1:n.*3239del
ENST00000637038.1:c.2608del
ENST00000637988.1:c.5713del ENSP00000490780.1:p.Glu1905LysfsTer16
ENST00000640036.1:c.5713del ENSP00000491573.1:p.Glu1905LysfsTer16
ENST00000641575.1:c.5710del ENSP00000492917.1:p.Glu1904LysfsTer16
ENST00000641603.1:c.5464del ENSP00000492945.1:p.Glu1822LysfsTer16
ENST00000641996.1:c.*5300del ENSP00000493054.1:n.*5300del
ENST00000671940.1:c.*3689del ENSP00000500336.1:n.*3689del
ENST00000673490.1:n.8219del
ENST00000674923.1:c.5746del MANE Select ENSP00000501589.1:p.Glu1916LysfsTer16
ENST00000303395.8:c.5746del ENSP00000303540.4:p.Glu1916LysfsTer16
ENST00000375405.7:c.5713del ENSP00000364554.3:p.Glu1905LysfsTer16
ENST00000409050.1:c.5662del ENSP00000386312.1:p.Glu1888LysfsTer16
ENST00000423058.6:c.5746del ENSP00000407030.2:p.Glu1916LysfsTer16
NM_001165963.1:c.5746del NP_001159435.1:p.Glu1916LysfsTer16
NM_001165964.1:c.5662del NP_001159436.1:p.Glu1888LysfsTer16
NM_001202435.1:c.5746del NP_001189364.1:p.Glu1916LysfsTer16
NM_006920.4:c.5713del , LRG_8t1:c.5713del NP_008851.3:p.Glu1905LysfsTer16
NR_110598.1:n.176-24083del
XM_011511598.1:c.5746del XP_011509900.1:p.Glu1916LysfsTer16
XM_011511599.1:c.5746del XP_011509901.1:p.Glu1916LysfsTer16
XM_011511600.1:c.5746del XP_011509902.1:p.Glu1916LysfsTer16
XM_011511601.1:c.5746del XP_011509903.1:p.Glu1916LysfsTer16
XM_011511602.1:c.5746del XP_011509904.1:p.Glu1916LysfsTer16
XM_011511603.1:c.5743del XP_011509905.1:p.Glu1915LysfsTer16
XM_011511604.1:c.5713del XP_011509906.1:p.Glu1905LysfsTer16
XM_011511605.1:c.5710del XP_011509907.1:p.Glu1904LysfsTer16
XM_011511606.1:c.5662del XP_011509908.1:p.Glu1888LysfsTer16
XM_011511607.1:c.5464del XP_011509909.1:p.Glu1822LysfsTer16
NM_001165963.2:c.5746del NP_001159435.1:p.Glu1916LysfsTer16
NM_001165964.2:c.5662del NP_001159436.1:p.Glu1888LysfsTer16
NM_001202435.2:c.5746del NP_001189364.1:p.Glu1916LysfsTer16
NM_001353948.1:c.5746del NP_001340877.1:p.Glu1916LysfsTer16
NM_001353949.1:c.5713del NP_001340878.1:p.Glu1905LysfsTer16
NM_001353950.1:c.5713del NP_001340879.1:p.Glu1905LysfsTer16
NM_001353951.1:c.5713del NP_001340880.1:p.Glu1905LysfsTer16
NM_001353952.1:c.5713del NP_001340881.1:p.Glu1905LysfsTer16
NM_001353954.1:c.5710del NP_001340883.1:p.Glu1904LysfsTer16
NM_001353955.1:c.5710del NP_001340884.1:p.Glu1904LysfsTer16
NM_001353957.1:c.5662del NP_001340886.1:p.Glu1888LysfsTer16
NM_001353958.1:c.5662del NP_001340887.1:p.Glu1888LysfsTer16
NM_001353960.1:c.5659del NP_001340889.1:p.Glu1887LysfsTer16
NM_001353961.1:c.3304del NP_001340890.1:p.Glu1102LysfsTer16
NM_006920.5:c.5713del NP_008851.3:p.Glu1905LysfsTer16
NR_148667.1:n.6182del
XR_001738883.1:n.6196del
XR_001738884.1:n.6168del
NM_001165963.3:c.5746del NP_001159435.1:p.Glu1916LysfsTer16
NM_001165964.3:c.5662del NP_001159436.1:p.Glu1888LysfsTer16
NM_001202435.3:c.5746del NP_001189364.1:p.Glu1916LysfsTer16
NM_001353948.2:c.5746del NP_001340877.1:p.Glu1916LysfsTer16
NM_001353949.2:c.5713del NP_001340878.1:p.Glu1905LysfsTer16
NM_001353950.2:c.5713del NP_001340879.1:p.Glu1905LysfsTer16
NM_001353951.2:c.5713del NP_001340880.1:p.Glu1905LysfsTer16
NM_001353952.2:c.5713del NP_001340881.1:p.Glu1905LysfsTer16
NM_001353954.2:c.5710del NP_001340883.1:p.Glu1904LysfsTer16
NM_001353955.2:c.5710del NP_001340884.1:p.Glu1904LysfsTer16
NM_001353957.2:c.5662del NP_001340886.1:p.Glu1888LysfsTer16
NM_001353958.2:c.5662del NP_001340887.1:p.Glu1888LysfsTer16
NM_001353960.2:c.5659del NP_001340889.1:p.Glu1887LysfsTer16
NM_001353961.2:c.3304del NP_001340890.1:p.Glu1102LysfsTer16
NM_006920.6:c.5713del NP_008851.3:p.Glu1905LysfsTer16
NR_148667.2:n.6163del
NM_001165963.4:c.5746del MANE Select NP_001159435.1:p.Glu1916LysfsTer16