Canonical Allele Identifier: CA16042389
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 373157
ClinVar RCV Id: RCV000412769
dbSNP Id: rs1057518258

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165992030C>T , CM000664.2:g.165992030C>T GRCh38
NC_000002.11:g.166848540C>T , CM000664.1:g.166848540C>T GRCh37
NC_000002.10:g.166556786C>T NCBI36
NG_011906.1:g.86610G>A , LRG_8:g.86610G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*3281G>A ENSP00000509637.1:n.*3281G>A
ENST00000303395.9:c.5245G>A ENSP00000303540.4:p.Gly1749Arg
ENST00000635750.1:c.5212G>A ENSP00000490799.1:p.Gly1738Arg
ENST00000635776.1:c.*2078G>A ENSP00000490692.1:n.*2078G>A
ENST00000636194.1:c.*2738G>A ENSP00000490288.1:n.*2738G>A
ENST00000637038.1:n.2107G>A
ENST00000637988.1:c.5212G>A ENSP00000490780.1:p.Gly1738Arg
ENST00000640036.1:c.5212G>A ENSP00000491573.1:p.Gly1738Arg
ENST00000641575.1:c.5209G>A ENSP00000492917.1:p.Gly1737Arg
ENST00000641603.1:c.4963G>A ENSP00000492945.1:p.Gly1655Arg
ENST00000641996.1:c.*4799G>A ENSP00000493054.1:n.*4799G>A
ENST00000671940.1:c.*3188G>A ENSP00000500336.1:n.*3188G>A
ENST00000673490.1:n.7718G>A
ENST00000674923.1:c.5245G>A MANE Select ENSP00000501589.1:p.Gly1749Arg
ENST00000303395.8:c.5245G>A ENSP00000303540.4:p.Gly1749Arg
ENST00000375405.7:c.5212G>A ENSP00000364554.3:p.Gly1738Arg
ENST00000409050.1:n.5161G>A ENSP00000386312.1:p.Gly1721Arg
ENST00000423058.6:c.5245G>A ENSP00000407030.2:p.Gly1749Arg
NM_001165963.1:c.5245G>A NP_001159435.1:p.Gly1749Arg
NM_001165964.1:c.5161G>A NP_001159436.1:p.Gly1721Arg
NM_001202435.1:c.5245G>A NP_001189364.1:p.Gly1749Arg
NM_006920.4:c.5212G>A , LRG_8t1:c.5212G>A NP_008851.3:p.Gly1738Arg
NR_110598.1:n.176-23583C>T
XM_011511598.1:c.5245G>A XP_011509900.1:p.Gly1749Arg
XM_011511599.1:c.5245G>A XP_011509901.1:p.Gly1749Arg
XM_011511600.1:c.5245G>A XP_011509902.1:p.Gly1749Arg
XM_011511601.1:c.5245G>A XP_011509903.1:p.Gly1749Arg
XM_011511602.1:c.5245G>A XP_011509904.1:p.Gly1749Arg
XM_011511603.1:c.5242G>A XP_011509905.1:p.Gly1748Arg
XM_011511604.1:c.5212G>A XP_011509906.1:p.Gly1738Arg
XM_011511605.1:c.5209G>A XP_011509907.1:p.Gly1737Arg
XM_011511606.1:c.5161G>A XP_011509908.1:p.Gly1721Arg
XM_011511607.1:c.4963G>A XP_011509909.1:p.Gly1655Arg
NM_001165963.2:c.5245G>A NP_001159435.1:p.Gly1749Arg
NM_001165964.2:c.5161G>A NP_001159436.1:p.Gly1721Arg
NM_001202435.2:c.5245G>A NP_001189364.1:p.Gly1749Arg
NM_001353948.1:c.5245G>A NP_001340877.1:p.Gly1749Arg
NM_001353949.1:c.5212G>A NP_001340878.1:p.Gly1738Arg
NM_001353950.1:c.5212G>A NP_001340879.1:p.Gly1738Arg
NM_001353951.1:c.5212G>A NP_001340880.1:p.Gly1738Arg
NM_001353952.1:c.5212G>A NP_001340881.1:p.Gly1738Arg
NM_001353954.1:c.5209G>A NP_001340883.1:p.Gly1737Arg
NM_001353955.1:c.5209G>A NP_001340884.1:p.Gly1737Arg
NM_001353957.1:c.5161G>A NP_001340886.1:p.Gly1721Arg
NM_001353958.1:c.5161G>A NP_001340887.1:p.Gly1721Arg
NM_001353960.1:c.5158G>A NP_001340889.1:p.Gly1720Arg
NM_001353961.1:c.2803G>A NP_001340890.1:p.Gly935Arg
NM_006920.5:c.5212G>A NP_008851.3:p.Gly1738Arg
NR_148667.1:n.5681G>A
XR_001738883.1:n.5695G>A
XR_001738884.1:n.5667G>A
NM_001165963.3:c.5245G>A NP_001159435.1:p.Gly1749Arg
NM_001165964.3:c.5161G>A NP_001159436.1:p.Gly1721Arg
NM_001202435.3:c.5245G>A NP_001189364.1:p.Gly1749Arg
NM_001353948.2:c.5245G>A NP_001340877.1:p.Gly1749Arg
NM_001353949.2:c.5212G>A NP_001340878.1:p.Gly1738Arg
NM_001353950.2:c.5212G>A NP_001340879.1:p.Gly1738Arg
NM_001353951.2:c.5212G>A NP_001340880.1:p.Gly1738Arg
NM_001353952.2:c.5212G>A NP_001340881.1:p.Gly1738Arg
NM_001353954.2:c.5209G>A NP_001340883.1:p.Gly1737Arg
NM_001353955.2:c.5209G>A NP_001340884.1:p.Gly1737Arg
NM_001353957.2:c.5161G>A NP_001340886.1:p.Gly1721Arg
NM_001353958.2:c.5161G>A NP_001340887.1:p.Gly1721Arg
NM_001353960.2:c.5158G>A NP_001340889.1:p.Gly1720Arg
NM_001353961.2:c.2803G>A NP_001340890.1:p.Gly935Arg
NM_006920.6:c.5212G>A NP_008851.3:p.Gly1738Arg
NR_148667.2:n.5662G>A
NM_001165963.4:c.5245G>A MANE Select NP_001159435.1:p.Gly1749Arg