Canonical Allele Identifier: CA303489
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189988
ClinVar RCV Id: RCV000180944
dbSNP Id: rs794726819

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165992279_165992282dup , CM000664.2:g.165992279_165992282dup GRCh38
NC_000002.11:g.166848789_166848792dup , CM000664.1:g.166848789_166848792dup GRCh37
NC_000002.10:g.166557035_166557038dup NCBI36
NG_011906.1:g.86358_86361dup , LRG_8:g.86358_86361dup

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*3029_*3032dup ENSP00000509637.1:n.*3029_*3032dup
ENST00000303395.9:c.4993_4996dup ENSP00000303540.4:p.Ser1666TyrfsTer8
ENST00000635750.1:c.4960_4963dup ENSP00000490799.1:p.Ser1655TyrfsTer8
ENST00000635776.1:c.*1826_*1829dup ENSP00000490692.1:n.*1826_*1829dup
ENST00000636194.1:c.*2486_*2489dup ENSP00000490288.1:n.*2486_*2489dup
ENST00000637038.1:c.1855_1858dup
ENST00000637988.1:c.4960_4963dup ENSP00000490780.1:p.Ser1655TyrfsTer8
ENST00000640036.1:c.4960_4963dup ENSP00000491573.1:p.Ser1655TyrfsTer8
ENST00000641575.1:c.4957_4960dup ENSP00000492917.1:p.Ser1654TyrfsTer8
ENST00000641603.1:c.4711_4714dup ENSP00000492945.1:p.Ser1572TyrfsTer8
ENST00000641996.1:c.*4547_*4550dup ENSP00000493054.1:n.*4547_*4550dup
ENST00000671940.1:c.*2936_*2939dup ENSP00000500336.1:n.*2936_*2939dup
ENST00000673490.1:n.7466_7469dup
ENST00000674923.1:c.4993_4996dup MANE Select ENSP00000501589.1:p.Ser1666TyrfsTer8
ENST00000303395.8:c.4993_4996dup ENSP00000303540.4:p.Ser1666TyrfsTer8
ENST00000375405.7:c.4960_4963dup ENSP00000364554.3:p.Ser1655TyrfsTer8
ENST00000409050.1:c.4909_4912dup ENSP00000386312.1:p.Ser1638TyrfsTer8
ENST00000423058.6:c.4993_4996dup ENSP00000407030.2:p.Ser1666TyrfsTer8
NM_001165963.1:c.4993_4996dup NP_001159435.1:p.Ser1666TyrfsTer8
NM_001165964.1:c.4909_4912dup NP_001159436.1:p.Ser1638TyrfsTer8
NM_001202435.1:c.4993_4996dup NP_001189364.1:p.Ser1666TyrfsTer8
NM_006920.4:c.4960_4963dup , LRG_8t1:c.4960_4963dup NP_008851.3:p.Ser1655TyrfsTer8
NR_110598.1:n.176-23334_176-23331dup
XM_011511598.1:c.4993_4996dup XP_011509900.1:p.Ser1666TyrfsTer8
XM_011511599.1:c.4993_4996dup XP_011509901.1:p.Ser1666TyrfsTer8
XM_011511600.1:c.4993_4996dup XP_011509902.1:p.Ser1666TyrfsTer8
XM_011511601.1:c.4993_4996dup XP_011509903.1:p.Ser1666TyrfsTer8
XM_011511602.1:c.4993_4996dup XP_011509904.1:p.Ser1666TyrfsTer8
XM_011511603.1:c.4990_4993dup XP_011509905.1:p.Ser1665TyrfsTer8
XM_011511604.1:c.4960_4963dup XP_011509906.1:p.Ser1655TyrfsTer8
XM_011511605.1:c.4957_4960dup XP_011509907.1:p.Ser1654TyrfsTer8
XM_011511606.1:c.4909_4912dup XP_011509908.1:p.Ser1638TyrfsTer8
XM_011511607.1:c.4711_4714dup XP_011509909.1:p.Ser1572TyrfsTer8
NM_001165963.2:c.4993_4996dup NP_001159435.1:p.Ser1666TyrfsTer8
NM_001165964.2:c.4909_4912dup NP_001159436.1:p.Ser1638TyrfsTer8
NM_001202435.2:c.4993_4996dup NP_001189364.1:p.Ser1666TyrfsTer8
NM_001353948.1:c.4993_4996dup NP_001340877.1:p.Ser1666TyrfsTer8
NM_001353949.1:c.4960_4963dup NP_001340878.1:p.Ser1655TyrfsTer8
NM_001353950.1:c.4960_4963dup NP_001340879.1:p.Ser1655TyrfsTer8
NM_001353951.1:c.4960_4963dup NP_001340880.1:p.Ser1655TyrfsTer8
NM_001353952.1:c.4960_4963dup NP_001340881.1:p.Ser1655TyrfsTer8
NM_001353954.1:c.4957_4960dup NP_001340883.1:p.Ser1654TyrfsTer8
NM_001353955.1:c.4957_4960dup NP_001340884.1:p.Ser1654TyrfsTer8
NM_001353957.1:c.4909_4912dup NP_001340886.1:p.Ser1638TyrfsTer8
NM_001353958.1:c.4909_4912dup NP_001340887.1:p.Ser1638TyrfsTer8
NM_001353960.1:c.4906_4909dup NP_001340889.1:p.Ser1637TyrfsTer8
NM_001353961.1:c.2551_2554dup NP_001340890.1:p.Ser852TyrfsTer8
NM_006920.5:c.4960_4963dup NP_008851.3:p.Ser1655TyrfsTer8
NR_148667.1:n.5429_5432dup
XR_001738883.1:n.5443_5446dup
XR_001738884.1:n.5415_5418dup
NM_001165963.3:c.4993_4996dup NP_001159435.1:p.Ser1666TyrfsTer8
NM_001165964.3:c.4909_4912dup NP_001159436.1:p.Ser1638TyrfsTer8
NM_001202435.3:c.4993_4996dup NP_001189364.1:p.Ser1666TyrfsTer8
NM_001353948.2:c.4993_4996dup NP_001340877.1:p.Ser1666TyrfsTer8
NM_001353949.2:c.4960_4963dup NP_001340878.1:p.Ser1655TyrfsTer8
NM_001353950.2:c.4960_4963dup NP_001340879.1:p.Ser1655TyrfsTer8
NM_001353951.2:c.4960_4963dup NP_001340880.1:p.Ser1655TyrfsTer8
NM_001353952.2:c.4960_4963dup NP_001340881.1:p.Ser1655TyrfsTer8
NM_001353954.2:c.4957_4960dup NP_001340883.1:p.Ser1654TyrfsTer8
NM_001353955.2:c.4957_4960dup NP_001340884.1:p.Ser1654TyrfsTer8
NM_001353957.2:c.4909_4912dup NP_001340886.1:p.Ser1638TyrfsTer8
NM_001353958.2:c.4909_4912dup NP_001340887.1:p.Ser1638TyrfsTer8
NM_001353960.2:c.4906_4909dup NP_001340889.1:p.Ser1637TyrfsTer8
NM_001353961.2:c.2551_2554dup NP_001340890.1:p.Ser852TyrfsTer8
NM_006920.6:c.4960_4963dup NP_008851.3:p.Ser1655TyrfsTer8
NR_148667.2:n.5410_5413dup
NM_001165963.4:c.4993_4996dup MANE Select NP_001159435.1:p.Ser1666TyrfsTer8