Canonical Allele Identifier: CA349049871

Gene: SCN1A

Linked Data

• ClinVar Variation Id: 1804043
• ClinVar RCV Id: RCV002468781
• dbSNP Id: rs1553524889
• MyVariant Identifiers: chr2:g.166858987G>A (hg19) ; chr2:g.166002477G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166002477G>A , CM000664.2:g.166002477G>A	GRCh38
NC_000002.11:g.166858987G>A , CM000664.1:g.166858987G>A	GRCh37
NC_000002.10:g.166567233G>A	NCBI36
NG_011906.1:g.76163C>T , LRG_8:g.76163C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689288.1:c.*2315C>T	ENSP00000509637.1:n.*2315C>T
ENST00000303395.9:c.4279C>T	ENSP00000303540.4:p.Gln1427Ter
ENST00000635750.1:c.4246C>T	ENSP00000490799.1:p.Gln1416Ter
ENST00000635776.1:c.4246C>T	ENSP00000490692.1:p.Gln1416Ter
ENST00000635893.1:c.10C>T	ENSP00000489986.1:p.Gln4Ter
ENST00000636194.1:c.*1772C>T	ENSP00000490288.1:n.*1772C>T
ENST00000637038.1:c.1141C>T
ENST00000637988.1:c.4246C>T	ENSP00000490780.1:p.Gln1416Ter
ENST00000640036.1:c.4246C>T	ENSP00000491573.1:p.Gln1416Ter
ENST00000641575.1:c.4243C>T	ENSP00000492917.1:p.Gln1415Ter
ENST00000641603.1:c.4003-2701C>T	ENSP00000492945.1:n.4003-2701C>T
ENST00000641996.1:c.*3833C>T	ENSP00000493054.1:n.*3833C>T
ENST00000671940.1:c.*2222C>T	ENSP00000500336.1:n.*2222C>T
ENST00000673490.1:n.6752C>T
ENST00000674923.1:c.4279C>T MANE Select	ENSP00000501589.1:p.Gln1427Ter
ENST00000303395.8:c.4279C>T	ENSP00000303540.4:p.Gln1427Ter
ENST00000375405.7:c.4246C>T	ENSP00000364554.3:p.Gln1416Ter
ENST00000409050.1:c.4195C>T	ENSP00000386312.1:p.Gln1399Ter
ENST00000423058.6:c.4279C>T	ENSP00000407030.2:p.Gln1427Ter
ENST00000491429.1:n.432C>T
NM_001165963.1:c.4279C>T	NP_001159435.1:p.Gln1427Ter
NM_001165964.1:c.4195C>T	NP_001159436.1:p.Gln1399Ter
NM_001202435.1:c.4279C>T	NP_001189364.1:p.Gln1427Ter
NM_006920.4:c.4246C>T , LRG_8t1:c.4246C>T	NP_008851.3:p.Gln1416Ter
NR_110598.1:n.176-13136G>A
XM_011511598.1:c.4279C>T	XP_011509900.1:p.Gln1427Ter
XM_011511599.1:c.4279C>T	XP_011509901.1:p.Gln1427Ter
XM_011511600.1:c.4279C>T	XP_011509902.1:p.Gln1427Ter
XM_011511601.1:c.4279C>T	XP_011509903.1:p.Gln1427Ter
XM_011511602.1:c.4279C>T	XP_011509904.1:p.Gln1427Ter
XM_011511603.1:c.4276C>T	XP_011509905.1:p.Gln1426Ter
XM_011511604.1:c.4246C>T	XP_011509906.1:p.Gln1416Ter
XM_011511605.1:c.4243C>T	XP_011509907.1:p.Gln1415Ter
XM_011511606.1:c.4195C>T	XP_011509908.1:p.Gln1399Ter
XM_011511607.1:c.4003-2701C>T	XP_011509909.1:n.4003-2701C>T
XR_922981.1:n.4527C>T
NM_001165963.2:c.4279C>T	NP_001159435.1:p.Gln1427Ter
NM_001165964.2:c.4195C>T	NP_001159436.1:p.Gln1399Ter
NM_001202435.2:c.4279C>T	NP_001189364.1:p.Gln1427Ter
NM_001353948.1:c.4279C>T	NP_001340877.1:p.Gln1427Ter
NM_001353949.1:c.4246C>T	NP_001340878.1:p.Gln1416Ter
NM_001353950.1:c.4246C>T	NP_001340879.1:p.Gln1416Ter
NM_001353951.1:c.4246C>T	NP_001340880.1:p.Gln1416Ter
NM_001353952.1:c.4246C>T	NP_001340881.1:p.Gln1416Ter
NM_001353954.1:c.4243C>T	NP_001340883.1:p.Gln1415Ter
NM_001353955.1:c.4243C>T	NP_001340884.1:p.Gln1415Ter
NM_001353957.1:c.4195C>T	NP_001340886.1:p.Gln1399Ter
NM_001353958.1:c.4195C>T	NP_001340887.1:p.Gln1399Ter
NM_001353960.1:c.4192C>T	NP_001340889.1:p.Gln1398Ter
NM_001353961.1:c.1837C>T	NP_001340890.1:p.Gln613Ter
NM_006920.5:c.4246C>T	NP_008851.3:p.Gln1416Ter
NR_148667.1:n.4715C>T
XR_001738883.1:n.4729C>T
XR_001738884.1:n.4701C>T
NM_001165963.3:c.4279C>T	NP_001159435.1:p.Gln1427Ter
NM_001165964.3:c.4195C>T	NP_001159436.1:p.Gln1399Ter
NM_001202435.3:c.4279C>T	NP_001189364.1:p.Gln1427Ter
NM_001353948.2:c.4279C>T	NP_001340877.1:p.Gln1427Ter
NM_001353949.2:c.4246C>T	NP_001340878.1:p.Gln1416Ter
NM_001353950.2:c.4246C>T	NP_001340879.1:p.Gln1416Ter
NM_001353951.2:c.4246C>T	NP_001340880.1:p.Gln1416Ter
NM_001353952.2:c.4246C>T	NP_001340881.1:p.Gln1416Ter
NM_001353954.2:c.4243C>T	NP_001340883.1:p.Gln1415Ter
NM_001353955.2:c.4243C>T	NP_001340884.1:p.Gln1415Ter
NM_001353957.2:c.4195C>T	NP_001340886.1:p.Gln1399Ter
NM_001353958.2:c.4195C>T	NP_001340887.1:p.Gln1399Ter
NM_001353960.2:c.4192C>T	NP_001340889.1:p.Gln1398Ter
NM_001353961.2:c.1837C>T	NP_001340890.1:p.Gln613Ter
NM_006920.6:c.4246C>T	NP_008851.3:p.Gln1416Ter
NR_148667.2:n.4696C>T
NM_001165963.4:c.4279C>T MANE Select	NP_001159435.1:p.Gln1427Ter