Canonical Allele Identifier: CA285024
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68571
dbSNP Id: rs121917921

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165991927G>A , CM000664.2:g.165991927G>A GRCh38
NC_000002.11:g.166848437G>A , CM000664.1:g.166848437G>A GRCh37
NC_000002.10:g.166556683G>A NCBI36
NG_011906.1:g.86713C>T , LRG_8:g.86713C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*3384C>T ENSP00000509637.1:n.*3384C>T
ENST00000303395.9:c.5348C>T ENSP00000303540.4:p.Ala1783Val
ENST00000635750.1:c.5315C>T ENSP00000490799.1:p.Ala1772Val
ENST00000635776.1:c.*2181C>T ENSP00000490692.1:n.*2181C>T
ENST00000636194.1:c.*2841C>T ENSP00000490288.1:n.*2841C>T
ENST00000637038.1:n.2210C>T
ENST00000637988.1:c.5315C>T ENSP00000490780.1:p.Ala1772Val
ENST00000640036.1:c.5315C>T ENSP00000491573.1:p.Ala1772Val
ENST00000641575.1:c.5312C>T ENSP00000492917.1:p.Ala1771Val
ENST00000641603.1:c.5066C>T ENSP00000492945.1:p.Ala1689Val
ENST00000641996.1:c.*4902C>T ENSP00000493054.1:n.*4902C>T
ENST00000671940.1:c.*3291C>T ENSP00000500336.1:n.*3291C>T
ENST00000673490.1:n.7821C>T
ENST00000674923.1:c.5348C>T MANE Select ENSP00000501589.1:p.Ala1783Val
ENST00000303395.8:c.5348C>T ENSP00000303540.4:p.Ala1783Val
ENST00000375405.7:c.5315C>T ENSP00000364554.3:p.Ala1772Val
ENST00000409050.1:n.5264C>T ENSP00000386312.1:p.Ala1755Val
ENST00000423058.6:c.5348C>T ENSP00000407030.2:p.Ala1783Val
NM_001165963.1:c.5348C>T NP_001159435.1:p.Ala1783Val
NM_001165964.1:c.5264C>T NP_001159436.1:p.Ala1755Val
NM_001202435.1:c.5348C>T NP_001189364.1:p.Ala1783Val
NM_006920.4:c.5315C>T , LRG_8t1:c.5315C>T NP_008851.3:p.Ala1772Val
NR_110598.1:n.176-23686G>A
XM_011511598.1:c.5348C>T XP_011509900.1:p.Ala1783Val
XM_011511599.1:c.5348C>T XP_011509901.1:p.Ala1783Val
XM_011511600.1:c.5348C>T XP_011509902.1:p.Ala1783Val
XM_011511601.1:c.5348C>T XP_011509903.1:p.Ala1783Val
XM_011511602.1:c.5348C>T XP_011509904.1:p.Ala1783Val
XM_011511603.1:c.5345C>T XP_011509905.1:p.Ala1782Val
XM_011511604.1:c.5315C>T XP_011509906.1:p.Ala1772Val
XM_011511605.1:c.5312C>T XP_011509907.1:p.Ala1771Val
XM_011511606.1:c.5264C>T XP_011509908.1:p.Ala1755Val
XM_011511607.1:c.5066C>T XP_011509909.1:p.Ala1689Val
NM_001165963.2:c.5348C>T NP_001159435.1:p.Ala1783Val
NM_001165964.2:c.5264C>T NP_001159436.1:p.Ala1755Val
NM_001202435.2:c.5348C>T NP_001189364.1:p.Ala1783Val
NM_001353948.1:c.5348C>T NP_001340877.1:p.Ala1783Val
NM_001353949.1:c.5315C>T NP_001340878.1:p.Ala1772Val
NM_001353950.1:c.5315C>T NP_001340879.1:p.Ala1772Val
NM_001353951.1:c.5315C>T NP_001340880.1:p.Ala1772Val
NM_001353952.1:c.5315C>T NP_001340881.1:p.Ala1772Val
NM_001353954.1:c.5312C>T NP_001340883.1:p.Ala1771Val
NM_001353955.1:c.5312C>T NP_001340884.1:p.Ala1771Val
NM_001353957.1:c.5264C>T NP_001340886.1:p.Ala1755Val
NM_001353958.1:c.5264C>T NP_001340887.1:p.Ala1755Val
NM_001353960.1:c.5261C>T NP_001340889.1:p.Ala1754Val
NM_001353961.1:c.2906C>T NP_001340890.1:p.Ala969Val
NM_006920.5:c.5315C>T NP_008851.3:p.Ala1772Val
NR_148667.1:n.5784C>T
XR_001738883.1:n.5798C>T
XR_001738884.1:n.5770C>T
NM_001165963.3:c.5348C>T NP_001159435.1:p.Ala1783Val
NM_001165964.3:c.5264C>T NP_001159436.1:p.Ala1755Val
NM_001202435.3:c.5348C>T NP_001189364.1:p.Ala1783Val
NM_001353948.2:c.5348C>T NP_001340877.1:p.Ala1783Val
NM_001353949.2:c.5315C>T NP_001340878.1:p.Ala1772Val
NM_001353950.2:c.5315C>T NP_001340879.1:p.Ala1772Val
NM_001353951.2:c.5315C>T NP_001340880.1:p.Ala1772Val
NM_001353952.2:c.5315C>T NP_001340881.1:p.Ala1772Val
NM_001353954.2:c.5312C>T NP_001340883.1:p.Ala1771Val
NM_001353955.2:c.5312C>T NP_001340884.1:p.Ala1771Val
NM_001353957.2:c.5264C>T NP_001340886.1:p.Ala1755Val
NM_001353958.2:c.5264C>T NP_001340887.1:p.Ala1755Val
NM_001353960.2:c.5261C>T NP_001340889.1:p.Ala1754Val
NM_001353961.2:c.2906C>T NP_001340890.1:p.Ala969Val
NM_006920.6:c.5315C>T NP_008851.3:p.Ala1772Val
NR_148667.2:n.5765C>T
NM_001165963.4:c.5348C>T MANE Select NP_001159435.1:p.Ala1783Val