Canonical Allele Identifier: CA1304842394
Gene: SCN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166002473A= , CM000664.2:g.166002473A= GRCh38
NC_000002.11:g.166858983A= , CM000664.1:g.166858983A= GRCh37
NC_000002.10:g.166567229A= NCBI36
NG_011906.1:g.76167T= , LRG_8:g.76167T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689288.1:c.*2319T= ENSP00000509637.1:n.*2319T=
ENST00000303395.9:c.4283T= ENSP00000303540.4:p.Val1428=
ENST00000635750.1:c.4250T= ENSP00000490799.1:p.Val1417=
ENST00000635776.1:c.4250T= ENSP00000490692.1:p.Val1417=
ENST00000635893.1:c.14T= ENSP00000489986.1:p.Val5=
ENST00000636194.1:c.*1776T= ENSP00000490288.1:n.*1776T=
ENST00000637038.1:c.1145T=
ENST00000637988.1:c.4250T= ENSP00000490780.1:p.Val1417=
ENST00000640036.1:c.4250T= ENSP00000491573.1:p.Val1417=
ENST00000641575.1:c.4247T= ENSP00000492917.1:p.Val1416=
ENST00000641603.1:c.4003-2697T= ENSP00000492945.1:n.4003-2697T=
ENST00000641996.1:c.*3837T= ENSP00000493054.1:n.*3837T=
ENST00000671940.1:c.*2226T= ENSP00000500336.1:n.*2226T=
ENST00000673490.1:n.6756T=
ENST00000674923.1:c.4283T= MANE Select ENSP00000501589.1:p.Val1428=
ENST00000303395.8:c.4283T= ENSP00000303540.4:p.Val1428=
ENST00000375405.7:c.4250T= ENSP00000364554.3:p.Val1417=
ENST00000409050.1:c.4199T= ENSP00000386312.1:p.Val1400=
ENST00000423058.6:c.4283T= ENSP00000407030.2:p.Val1428=
ENST00000491429.1:n.436T=
NM_001165963.1:c.4283T= NP_001159435.1:p.Val1428=
NM_001165964.1:c.4199T= NP_001159436.1:p.Val1400=
NM_001202435.1:c.4283T= NP_001189364.1:p.Val1428=
NM_006920.4:c.4250T= , LRG_8t1:c.4250T= NP_008851.3:p.Val1417=
NR_110598.1:n.176-13140A=
XM_011511598.1:c.4283T= XP_011509900.1:p.Val1428=
XM_011511599.1:c.4283T= XP_011509901.1:p.Val1428=
XM_011511600.1:c.4283T= XP_011509902.1:p.Val1428=
XM_011511601.1:c.4283T= XP_011509903.1:p.Val1428=
XM_011511602.1:c.4283T= XP_011509904.1:p.Val1428=
XM_011511603.1:c.4280T= XP_011509905.1:p.Val1427=
XM_011511604.1:c.4250T= XP_011509906.1:p.Val1417=
XM_011511605.1:c.4247T= XP_011509907.1:p.Val1416=
XM_011511606.1:c.4199T= XP_011509908.1:p.Val1400=
XM_011511607.1:c.4003-2697T= XP_011509909.1:n.4003-2697T=
XR_922981.1:n.4531T=
NM_001165963.2:c.4283T= NP_001159435.1:p.Val1428=
NM_001165964.2:c.4199T= NP_001159436.1:p.Val1400=
NM_001202435.2:c.4283T= NP_001189364.1:p.Val1428=
NM_001353948.1:c.4283T= NP_001340877.1:p.Val1428=
NM_001353949.1:c.4250T= NP_001340878.1:p.Val1417=
NM_001353950.1:c.4250T= NP_001340879.1:p.Val1417=
NM_001353951.1:c.4250T= NP_001340880.1:p.Val1417=
NM_001353952.1:c.4250T= NP_001340881.1:p.Val1417=
NM_001353954.1:c.4247T= NP_001340883.1:p.Val1416=
NM_001353955.1:c.4247T= NP_001340884.1:p.Val1416=
NM_001353957.1:c.4199T= NP_001340886.1:p.Val1400=
NM_001353958.1:c.4199T= NP_001340887.1:p.Val1400=
NM_001353960.1:c.4196T= NP_001340889.1:p.Val1399=
NM_001353961.1:c.1841T= NP_001340890.1:p.Val614=
NM_006920.5:c.4250T= NP_008851.3:p.Val1417=
NR_148667.1:n.4719T=
XR_001738883.1:n.4733T=
XR_001738884.1:n.4705T=
NM_001165963.3:c.4283T= NP_001159435.1:p.Val1428=
NM_001165964.3:c.4199T= NP_001159436.1:p.Val1400=
NM_001202435.3:c.4283T= NP_001189364.1:p.Val1428=
NM_001353948.2:c.4283T= NP_001340877.1:p.Val1428=
NM_001353949.2:c.4250T= NP_001340878.1:p.Val1417=
NM_001353950.2:c.4250T= NP_001340879.1:p.Val1417=
NM_001353951.2:c.4250T= NP_001340880.1:p.Val1417=
NM_001353952.2:c.4250T= NP_001340881.1:p.Val1417=
NM_001353954.2:c.4247T= NP_001340883.1:p.Val1416=
NM_001353955.2:c.4247T= NP_001340884.1:p.Val1416=
NM_001353957.2:c.4199T= NP_001340886.1:p.Val1400=
NM_001353958.2:c.4199T= NP_001340887.1:p.Val1400=
NM_001353960.2:c.4196T= NP_001340889.1:p.Val1399=
NM_001353961.2:c.1841T= NP_001340890.1:p.Val614=
NM_006920.6:c.4250T= NP_008851.3:p.Val1417=
NR_148667.2:n.4700T=
NM_001165963.4:c.4283T= MANE Select NP_001159435.1:p.Val1428=