Canonical Allele Identifier: CA2586970226
Gene: SCN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165991648_165991655del , CM000664.2:g.165991648_165991655del GRCh38
NC_000002.11:g.166848158_166848165del , CM000664.1:g.166848158_166848165del GRCh37
NC_000002.10:g.166556404_166556411del NCBI36
NG_011906.1:g.86985_86992del , LRG_8:g.86985_86992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689288.1:c.*3656_*3663del ENSP00000509637.1:n.*3656_*3663del
ENST00000303395.9:c.5620_5627del ENSP00000303540.4:p.Val1875ArgfsTer?
ENST00000635750.1:c.5587_5594del ENSP00000490799.1:p.Val1864ArgfsTer?
ENST00000635776.1:c.*2453_*2460del ENSP00000490692.1:n.*2453_*2460del
ENST00000636194.1:c.*3113_*3120del ENSP00000490288.1:n.*3113_*3120del
ENST00000637038.1:c.2482_2489del
ENST00000637988.1:c.5587_5594del ENSP00000490780.1:p.Val1864ArgfsTer?
ENST00000640036.1:c.5587_5594del ENSP00000491573.1:p.Val1864ArgfsTer?
ENST00000641575.1:c.5584_5591del ENSP00000492917.1:p.Val1863ArgfsTer?
ENST00000641603.1:c.5338_5345del ENSP00000492945.1:p.Val1781ArgfsTer?
ENST00000641996.1:c.*5174_*5181del ENSP00000493054.1:n.*5174_*5181del
ENST00000671940.1:c.*3563_*3570del ENSP00000500336.1:n.*3563_*3570del
ENST00000673490.1:n.8093_8100del
ENST00000674923.1:c.5620_5627del MANE Select ENSP00000501589.1:p.Val1875ArgfsTer?
ENST00000303395.8:c.5620_5627del ENSP00000303540.4:p.Val1875ArgfsTer?
ENST00000375405.7:c.5587_5594del ENSP00000364554.3:p.Val1864ArgfsTer?
ENST00000409050.1:c.5536_5543del ENSP00000386312.1:p.Val1847ArgfsTer?
ENST00000423058.6:c.5620_5627del ENSP00000407030.2:p.Val1875ArgfsTer?
NM_001165963.1:c.5620_5627del NP_001159435.1:p.Val1875ArgfsTer?
NM_001165964.1:c.5536_5543del NP_001159436.1:p.Val1847ArgfsTer?
NM_001202435.1:c.5620_5627del NP_001189364.1:p.Val1875ArgfsTer?
NM_006920.4:c.5587_5594del , LRG_8t1:c.5587_5594del NP_008851.3:p.Val1864ArgfsTer?
NR_110598.1:n.176-23965_176-23958del
XM_011511598.1:c.5620_5627del XP_011509900.1:p.Val1875ArgfsTer?
XM_011511599.1:c.5620_5627del XP_011509901.1:p.Val1875ArgfsTer?
XM_011511600.1:c.5620_5627del XP_011509902.1:p.Val1875ArgfsTer?
XM_011511601.1:c.5620_5627del XP_011509903.1:p.Val1875ArgfsTer?
XM_011511602.1:c.5620_5627del XP_011509904.1:p.Val1875ArgfsTer?
XM_011511603.1:c.5617_5624del XP_011509905.1:p.Val1874ArgfsTer?
XM_011511604.1:c.5587_5594del XP_011509906.1:p.Val1864ArgfsTer?
XM_011511605.1:c.5584_5591del XP_011509907.1:p.Val1863ArgfsTer?
XM_011511606.1:c.5536_5543del XP_011509908.1:p.Val1847ArgfsTer?
XM_011511607.1:c.5338_5345del XP_011509909.1:p.Val1781ArgfsTer?
NM_001165963.2:c.5620_5627del NP_001159435.1:p.Val1875ArgfsTer?
NM_001165964.2:c.5536_5543del NP_001159436.1:p.Val1847ArgfsTer?
NM_001202435.2:c.5620_5627del NP_001189364.1:p.Val1875ArgfsTer?
NM_001353948.1:c.5620_5627del NP_001340877.1:p.Val1875ArgfsTer?
NM_001353949.1:c.5587_5594del NP_001340878.1:p.Val1864ArgfsTer?
NM_001353950.1:c.5587_5594del NP_001340879.1:p.Val1864ArgfsTer?
NM_001353951.1:c.5587_5594del NP_001340880.1:p.Val1864ArgfsTer?
NM_001353952.1:c.5587_5594del NP_001340881.1:p.Val1864ArgfsTer?
NM_001353954.1:c.5584_5591del NP_001340883.1:p.Val1863ArgfsTer?
NM_001353955.1:c.5584_5591del NP_001340884.1:p.Val1863ArgfsTer?
NM_001353957.1:c.5536_5543del NP_001340886.1:p.Val1847ArgfsTer?
NM_001353958.1:c.5536_5543del NP_001340887.1:p.Val1847ArgfsTer?
NM_001353960.1:c.5533_5540del NP_001340889.1:p.Val1846ArgfsTer?
NM_001353961.1:c.3178_3185del NP_001340890.1:p.Val1061ArgfsTer?
NM_006920.5:c.5587_5594del NP_008851.3:p.Val1864ArgfsTer?
NR_148667.1:n.6056_6063del
XR_001738883.1:n.6070_6077del
XR_001738884.1:n.6042_6049del
NM_001165963.3:c.5620_5627del NP_001159435.1:p.Val1875ArgfsTer?
NM_001165964.3:c.5536_5543del NP_001159436.1:p.Val1847ArgfsTer?
NM_001202435.3:c.5620_5627del NP_001189364.1:p.Val1875ArgfsTer?
NM_001353948.2:c.5620_5627del NP_001340877.1:p.Val1875ArgfsTer?
NM_001353949.2:c.5587_5594del NP_001340878.1:p.Val1864ArgfsTer?
NM_001353950.2:c.5587_5594del NP_001340879.1:p.Val1864ArgfsTer?
NM_001353951.2:c.5587_5594del NP_001340880.1:p.Val1864ArgfsTer?
NM_001353952.2:c.5587_5594del NP_001340881.1:p.Val1864ArgfsTer?
NM_001353954.2:c.5584_5591del NP_001340883.1:p.Val1863ArgfsTer?
NM_001353955.2:c.5584_5591del NP_001340884.1:p.Val1863ArgfsTer?
NM_001353957.2:c.5536_5543del NP_001340886.1:p.Val1847ArgfsTer?
NM_001353958.2:c.5536_5543del NP_001340887.1:p.Val1847ArgfsTer?
NM_001353960.2:c.5533_5540del NP_001340889.1:p.Val1846ArgfsTer?
NM_001353961.2:c.3178_3185del NP_001340890.1:p.Val1061ArgfsTer?
NM_006920.6:c.5587_5594del NP_008851.3:p.Val1864ArgfsTer?
NR_148667.2:n.6037_6044del
NM_001165963.4:c.5620_5627del MANE Select NP_001159435.1:p.Val1875ArgfsTer?