Canonical Allele Identifier: CA325463

Gene: SCN1A

Linked Data

• ClinVar Variation Id: 217247
• ClinVar RCV Id: RCV000201155 ; RCV001205577
• dbSNP Id: rs863225036
• MyVariant Identifiers: chr2:g.166852629T>C (hg19) ; chr2:g.165996119T>C (hg38)
• PubMed: PMID:21425109

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165996119T>C , CM000664.2:g.165996119T>C	GRCh38
NC_000002.11:g.166852629T>C , CM000664.1:g.166852629T>C	GRCh37
NC_000002.10:g.166560875T>C	NCBI36
NG_011906.1:g.82521A>G , LRG_8:g.82521A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689288.1:c.*2513-2A>G	ENSP00000509637.1:n.*2513-2A>G
ENST00000303395.9:c.4477-2A>G	ENSP00000303540.4:n.4477-2A>G
ENST00000635750.1:c.4444-2A>G	ENSP00000490799.1:n.4444-2A>G
ENST00000635776.1:c.4444-2A>G	ENSP00000490692.1:n.4444-2A>G
ENST00000636194.1:c.*1970-2A>G	ENSP00000490288.1:n.*1970-2A>G
ENST00000637038.1:c.1339-2A>G
ENST00000637988.1:c.4444-2A>G	ENSP00000490780.1:n.4444-2A>G
ENST00000640036.1:c.4444-2A>G	ENSP00000491573.1:n.4444-2A>G
ENST00000641575.1:c.4441-2A>G	ENSP00000492917.1:n.4441-2A>G
ENST00000641603.1:c.4195-2A>G	ENSP00000492945.1:n.4195-2A>G
ENST00000641996.1:c.*4031-2A>G	ENSP00000493054.1:n.*4031-2A>G
ENST00000671940.1:c.*2420-2A>G	ENSP00000500336.1:n.*2420-2A>G
ENST00000673490.1:n.6950-2A>G
ENST00000674923.1:c.4477-2A>G MANE Select	ENSP00000501589.1:n.4477-2A>G
ENST00000303395.8:c.4477-2A>G	ENSP00000303540.4:n.4477-2A>G
ENST00000375405.7:c.4444-2A>G	ENSP00000364554.3:n.4444-2A>G
ENST00000409050.1:c.4393-2A>G	ENSP00000386312.1:n.4393-2A>G
ENST00000423058.6:c.4477-2A>G	ENSP00000407030.2:n.4477-2A>G
ENST00000473295.2:n.480-2A>G
ENST00000625916.1:n.204A>G
NM_001165963.1:c.4477-2A>G	NP_001159435.1:n.4477-2A>G
NM_001165964.1:c.4393-2A>G	NP_001159436.1:n.4393-2A>G
NM_001202435.1:c.4477-2A>G	NP_001189364.1:n.4477-2A>G
NM_006920.4:c.4444-2A>G , LRG_8t1:c.4444-2A>G	NP_008851.3:n.4444-2A>G
NR_110598.1:n.176-19494T>C
XM_011511598.1:c.4477-2A>G	XP_011509900.1:n.4477-2A>G
XM_011511599.1:c.4477-2A>G	XP_011509901.1:n.4477-2A>G
XM_011511600.1:c.4477-2A>G	XP_011509902.1:n.4477-2A>G
XM_011511601.1:c.4477-2A>G	XP_011509903.1:n.4477-2A>G
XM_011511602.1:c.4477-2A>G	XP_011509904.1:n.4477-2A>G
XM_011511603.1:c.4474-2A>G	XP_011509905.1:n.4474-2A>G
XM_011511604.1:c.4444-2A>G	XP_011509906.1:n.4444-2A>G
XM_011511605.1:c.4441-2A>G	XP_011509907.1:n.4441-2A>G
XM_011511606.1:c.4393-2A>G	XP_011509908.1:n.4393-2A>G
XM_011511607.1:c.4195-2A>G	XP_011509909.1:n.4195-2A>G
NM_001165963.2:c.4477-2A>G	NP_001159435.1:n.4477-2A>G
NM_001165964.2:c.4393-2A>G	NP_001159436.1:n.4393-2A>G
NM_001202435.2:c.4477-2A>G	NP_001189364.1:n.4477-2A>G
NM_001353948.1:c.4477-2A>G	NP_001340877.1:n.4477-2A>G
NM_001353949.1:c.4444-2A>G	NP_001340878.1:n.4444-2A>G
NM_001353950.1:c.4444-2A>G	NP_001340879.1:n.4444-2A>G
NM_001353951.1:c.4444-2A>G	NP_001340880.1:n.4444-2A>G
NM_001353952.1:c.4444-2A>G	NP_001340881.1:n.4444-2A>G
NM_001353954.1:c.4441-2A>G	NP_001340883.1:n.4441-2A>G
NM_001353955.1:c.4441-2A>G	NP_001340884.1:n.4441-2A>G
NM_001353957.1:c.4393-2A>G	NP_001340886.1:n.4393-2A>G
NM_001353958.1:c.4393-2A>G	NP_001340887.1:n.4393-2A>G
NM_001353960.1:c.4390-2A>G	NP_001340889.1:n.4390-2A>G
NM_001353961.1:c.2035-2A>G	NP_001340890.1:n.2035-2A>G
NM_006920.5:c.4444-2A>G	NP_008851.3:n.4444-2A>G
NR_148667.1:n.4913-2A>G
XR_001738883.1:n.4927-2A>G
XR_001738884.1:n.4899-2A>G
NM_001165963.3:c.4477-2A>G	NP_001159435.1:n.4477-2A>G
NM_001165964.3:c.4393-2A>G	NP_001159436.1:n.4393-2A>G
NM_001202435.3:c.4477-2A>G	NP_001189364.1:n.4477-2A>G
NM_001353948.2:c.4477-2A>G	NP_001340877.1:n.4477-2A>G
NM_001353949.2:c.4444-2A>G	NP_001340878.1:n.4444-2A>G
NM_001353950.2:c.4444-2A>G	NP_001340879.1:n.4444-2A>G
NM_001353951.2:c.4444-2A>G	NP_001340880.1:n.4444-2A>G
NM_001353952.2:c.4444-2A>G	NP_001340881.1:n.4444-2A>G
NM_001353954.2:c.4441-2A>G	NP_001340883.1:n.4441-2A>G
NM_001353955.2:c.4441-2A>G	NP_001340884.1:n.4441-2A>G
NM_001353957.2:c.4393-2A>G	NP_001340886.1:n.4393-2A>G
NM_001353958.2:c.4393-2A>G	NP_001340887.1:n.4393-2A>G
NM_001353960.2:c.4390-2A>G	NP_001340889.1:n.4390-2A>G
NM_001353961.2:c.2035-2A>G	NP_001340890.1:n.2035-2A>G
NM_006920.6:c.4444-2A>G	NP_008851.3:n.4444-2A>G
NR_148667.2:n.4894-2A>G
NM_001165963.4:c.4477-2A>G MANE Select	NP_001159435.1:n.4477-2A>G