Canonical Allele Identifier: CA2573133507
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1454056
ClinVar RCV Id: RCV001939399
dbSNP Id: rs2105827355

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166041243_166041244insA , CM000664.2:g.166041243_166041244insA GRCh38
NC_000002.11:g.166897753_166897754insA , CM000664.1:g.166897753_166897754insA GRCh37
NC_000002.10:g.166605999_166606000insA NCBI36
NG_011906.1:g.37396_37397insT , LRG_8:g.37396_37397insT

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*438_*439insT ENSP00000509637.1:n.*438_*439insT
ENST00000303395.9:c.2402_2403insT ENSP00000303540.4:p.Val802SerfsTer?
ENST00000635750.1:c.2369_2370insT ENSP00000490799.1:p.Val791SerfsTer?
ENST00000635776.1:c.2369_2370insT ENSP00000490692.1:p.Val791SerfsTer?
ENST00000636194.1:c.2369_2370insT ENSP00000490288.1:p.Val791SerfsTer22
ENST00000636759.1:c.*2192_*2193insT ENSP00000490895.1:n.*2192_*2193insT
ENST00000637968.1:n.2654_2655insT
ENST00000637988.1:c.2369_2370insT ENSP00000490780.1:p.Val791SerfsTer?
ENST00000640036.1:c.2369_2370insT ENSP00000491573.1:p.Val791SerfsTer?
ENST00000641575.1:c.2366_2367insT ENSP00000492917.1:p.Val790SerfsTer?
ENST00000641603.1:c.2402_2403insT ENSP00000492945.1:p.Val802SerfsTer?
ENST00000641996.1:c.*1956_*1957insT ENSP00000493054.1:n.*1956_*1957insT
ENST00000671940.1:c.*345_*346insT ENSP00000500336.1:n.*345_*346insT
ENST00000673490.1:n.4875_4876insT
ENST00000674923.1:c.2402_2403insT MANE Select ENSP00000501589.1:p.Val802SerfsTer?
ENST00000303395.8:c.2402_2403insT ENSP00000303540.4:p.Val802SerfsTer?
ENST00000375405.7:c.2369_2370insT ENSP00000364554.3:p.Val791SerfsTer?
ENST00000409050.1:c.2318_2319insT ENSP00000386312.1:p.Val774SerfsTer?
ENST00000423058.6:c.2402_2403insT ENSP00000407030.2:p.Val802SerfsTer?
NM_001165963.1:c.2402_2403insT NP_001159435.1:p.Val802SerfsTer?
NM_001165964.1:c.2318_2319insT NP_001159436.1:p.Val774SerfsTer?
NM_001202435.1:c.2402_2403insT NP_001189364.1:p.Val802SerfsTer?
NM_006920.4:c.2369_2370insT , LRG_8t1:c.2369_2370insT NP_008851.3:p.Val791SerfsTer?
XM_011511598.1:c.2402_2403insT XP_011509900.1:p.Val802SerfsTer?
XM_011511599.1:c.2402_2403insT XP_011509901.1:p.Val802SerfsTer?
XM_011511600.1:c.2402_2403insT XP_011509902.1:p.Val802SerfsTer?
XM_011511601.1:c.2402_2403insT XP_011509903.1:p.Val802SerfsTer?
XM_011511602.1:c.2402_2403insT XP_011509904.1:p.Val802SerfsTer?
XM_011511603.1:c.2399_2400insT XP_011509905.1:p.Val801SerfsTer?
XM_011511604.1:c.2369_2370insT XP_011509906.1:p.Val791SerfsTer?
XM_011511605.1:c.2366_2367insT XP_011509907.1:p.Val790SerfsTer?
XM_011511606.1:c.2318_2319insT XP_011509908.1:p.Val774SerfsTer?
XM_011511607.1:c.2402_2403insT XP_011509909.1:p.Val802SerfsTer?
XR_922981.1:n.2586_2587insT
NM_001165963.2:c.2402_2403insT NP_001159435.1:p.Val802SerfsTer?
NM_001165964.2:c.2318_2319insT NP_001159436.1:p.Val774SerfsTer?
NM_001202435.2:c.2402_2403insT NP_001189364.1:p.Val802SerfsTer?
NM_001353948.1:c.2402_2403insT NP_001340877.1:p.Val802SerfsTer?
NM_001353949.1:c.2369_2370insT NP_001340878.1:p.Val791SerfsTer?
NM_001353950.1:c.2369_2370insT NP_001340879.1:p.Val791SerfsTer?
NM_001353951.1:c.2369_2370insT NP_001340880.1:p.Val791SerfsTer?
NM_001353952.1:c.2369_2370insT NP_001340881.1:p.Val791SerfsTer?
NM_001353954.1:c.2366_2367insT NP_001340883.1:p.Val790SerfsTer?
NM_001353955.1:c.2366_2367insT NP_001340884.1:p.Val790SerfsTer?
NM_001353957.1:c.2318_2319insT NP_001340886.1:p.Val774SerfsTer?
NM_001353958.1:c.2318_2319insT NP_001340887.1:p.Val774SerfsTer?
NM_001353960.1:c.2315_2316insT NP_001340889.1:p.Val773SerfsTer?
NM_001353961.1:c.-57_-56insT NP_001340890.1:n.-57_-56insT
NM_006920.5:c.2369_2370insT NP_008851.3:p.Val791SerfsTer?
NR_148667.1:n.2774_2775insT
XR_001738883.1:n.2788_2789insT
XR_001738884.1:n.2760_2761insT
NM_001165963.3:c.2402_2403insT NP_001159435.1:p.Val802SerfsTer?
NM_001165964.3:c.2318_2319insT NP_001159436.1:p.Val774SerfsTer?
NM_001202435.3:c.2402_2403insT NP_001189364.1:p.Val802SerfsTer?
NM_001353948.2:c.2402_2403insT NP_001340877.1:p.Val802SerfsTer?
NM_001353949.2:c.2369_2370insT NP_001340878.1:p.Val791SerfsTer?
NM_001353950.2:c.2369_2370insT NP_001340879.1:p.Val791SerfsTer?
NM_001353951.2:c.2369_2370insT NP_001340880.1:p.Val791SerfsTer?
NM_001353952.2:c.2369_2370insT NP_001340881.1:p.Val791SerfsTer?
NM_001353954.2:c.2366_2367insT NP_001340883.1:p.Val790SerfsTer?
NM_001353955.2:c.2366_2367insT NP_001340884.1:p.Val790SerfsTer?
NM_001353957.2:c.2318_2319insT NP_001340886.1:p.Val774SerfsTer?
NM_001353958.2:c.2318_2319insT NP_001340887.1:p.Val774SerfsTer?
NM_001353960.2:c.2315_2316insT NP_001340889.1:p.Val773SerfsTer?
NM_001353961.2:c.-57_-56insT NP_001340890.1:n.-57_-56insT
NM_006920.6:c.2369_2370insT NP_008851.3:p.Val791SerfsTer?
NR_148667.2:n.2755_2756insT
NM_001165963.4:c.2402_2403insT MANE Select NP_001159435.1:p.Val802SerfsTer?