Canonical Allele Identifier: CA16044313
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 375516
ClinVar RCV Id: RCV000416955
dbSNP Id: rs1057519534

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166013760dup , CM000664.2:g.166013760dup GRCh38
NC_000002.11:g.166870270dup , CM000664.1:g.166870270dup GRCh37
NC_000002.10:g.166578516dup NCBI36
NG_011906.1:g.64881dup , LRG_8:g.64881dup

Transcript Alleles

HGVS Amino-acid change
ENST00000689288.1:c.*1726dup ENSP00000509637.1:n.*1726dup
ENST00000303395.9:c.3690dup ENSP00000303540.4:p.Ser1231Ter
ENST00000635750.1:c.3657dup ENSP00000490799.1:p.Ser1220Ter
ENST00000635776.1:c.3657dup ENSP00000490692.1:p.Ser1220Ter
ENST00000636194.1:c.*1183dup ENSP00000490288.1:n.*1183dup
ENST00000637038.1:c.488dup
ENST00000637968.1:n.3942dup
ENST00000637988.1:c.3657dup ENSP00000490780.1:p.Ser1220Ter
ENST00000640036.1:c.3657dup ENSP00000491573.1:p.Ser1220Ter
ENST00000641575.1:c.3654dup ENSP00000492917.1:p.Ser1219Ter
ENST00000641603.1:c.3690dup ENSP00000492945.1:p.Ser1231Ter
ENST00000641996.1:c.*3244dup ENSP00000493054.1:n.*3244dup
ENST00000671940.1:c.*1633dup ENSP00000500336.1:n.*1633dup
ENST00000673490.1:n.6163dup
ENST00000674923.1:c.3690dup MANE Select ENSP00000501589.1:p.Ser1231Ter
ENST00000303395.8:c.3690dup ENSP00000303540.4:p.Ser1231Ter
ENST00000375405.7:c.3657dup ENSP00000364554.3:p.Ser1220Ter
ENST00000409050.1:c.3606dup ENSP00000386312.1:p.Ser1203Ter
ENST00000423058.6:c.3690dup ENSP00000407030.2:p.Ser1231Ter
NM_001165963.1:c.3690dup NP_001159435.1:p.Ser1231Ter
NM_001165964.1:c.3606dup NP_001159436.1:p.Ser1203Ter
NM_001202435.1:c.3690dup NP_001189364.1:p.Ser1231Ter
NM_006920.4:c.3657dup , LRG_8t1:c.3657dup NP_008851.3:p.Ser1220Ter
NR_110598.1:n.176-1853dup
XM_011511598.1:c.3690dup XP_011509900.1:p.Ser1231Ter
XM_011511599.1:c.3690dup XP_011509901.1:p.Ser1231Ter
XM_011511600.1:c.3690dup XP_011509902.1:p.Ser1231Ter
XM_011511601.1:c.3690dup XP_011509903.1:p.Ser1231Ter
XM_011511602.1:c.3690dup XP_011509904.1:p.Ser1231Ter
XM_011511603.1:c.3687dup XP_011509905.1:p.Ser1230Ter
XM_011511604.1:c.3657dup XP_011509906.1:p.Ser1220Ter
XM_011511605.1:c.3654dup XP_011509907.1:p.Ser1219Ter
XM_011511606.1:c.3606dup XP_011509908.1:p.Ser1203Ter
XM_011511607.1:c.3690dup XP_011509909.1:p.Ser1231Ter
XR_922981.1:n.3874dup
NM_001165963.2:c.3690dup NP_001159435.1:p.Ser1231Ter
NM_001165964.2:c.3606dup NP_001159436.1:p.Ser1203Ter
NM_001202435.2:c.3690dup NP_001189364.1:p.Ser1231Ter
NM_001353948.1:c.3690dup NP_001340877.1:p.Ser1231Ter
NM_001353949.1:c.3657dup NP_001340878.1:p.Ser1220Ter
NM_001353950.1:c.3657dup NP_001340879.1:p.Ser1220Ter
NM_001353951.1:c.3657dup NP_001340880.1:p.Ser1220Ter
NM_001353952.1:c.3657dup NP_001340881.1:p.Ser1220Ter
NM_001353954.1:c.3654dup NP_001340883.1:p.Ser1219Ter
NM_001353955.1:c.3654dup NP_001340884.1:p.Ser1219Ter
NM_001353957.1:c.3606dup NP_001340886.1:p.Ser1203Ter
NM_001353958.1:c.3606dup NP_001340887.1:p.Ser1203Ter
NM_001353960.1:c.3603dup NP_001340889.1:p.Ser1202Ter
NM_001353961.1:c.1248dup NP_001340890.1:p.Ser417Ter
NM_006920.5:c.3657dup NP_008851.3:p.Ser1220Ter
NR_148667.1:n.4062dup
XR_001738883.1:n.4076dup
XR_001738884.1:n.4048dup
NM_001165963.3:c.3690dup NP_001159435.1:p.Ser1231Ter
NM_001165964.3:c.3606dup NP_001159436.1:p.Ser1203Ter
NM_001202435.3:c.3690dup NP_001189364.1:p.Ser1231Ter
NM_001353948.2:c.3690dup NP_001340877.1:p.Ser1231Ter
NM_001353949.2:c.3657dup NP_001340878.1:p.Ser1220Ter
NM_001353950.2:c.3657dup NP_001340879.1:p.Ser1220Ter
NM_001353951.2:c.3657dup NP_001340880.1:p.Ser1220Ter
NM_001353952.2:c.3657dup NP_001340881.1:p.Ser1220Ter
NM_001353954.2:c.3654dup NP_001340883.1:p.Ser1219Ter
NM_001353955.2:c.3654dup NP_001340884.1:p.Ser1219Ter
NM_001353957.2:c.3606dup NP_001340886.1:p.Ser1203Ter
NM_001353958.2:c.3606dup NP_001340887.1:p.Ser1203Ter
NM_001353960.2:c.3603dup NP_001340889.1:p.Ser1202Ter
NM_001353961.2:c.1248dup NP_001340890.1:p.Ser417Ter
NM_006920.6:c.3657dup NP_008851.3:p.Ser1220Ter
NR_148667.2:n.4043dup
NM_001165963.4:c.3690dup MANE Select NP_001159435.1:p.Ser1231Ter