Canonical Allele Identifier: CA349064230

Gene: SCN1A

Linked Data

• MyVariant Identifiers: chr2:g.166897832G>C (hg19) ; chr2:g.166041322G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166041322G>C , CM000664.2:g.166041322G>C	GRCh38
NC_000002.11:g.166897832G>C , CM000664.1:g.166897832G>C	GRCh37
NC_000002.10:g.166606078G>C	NCBI36
NG_011906.1:g.37318C>G , LRG_8:g.37318C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689288.1:c.*360C>G	ENSP00000509637.1:n.*360C>G
ENST00000303395.9:c.2324C>G	ENSP00000303540.4:p.Thr775Ser
ENST00000635750.1:c.2291C>G	ENSP00000490799.1:p.Thr764Ser
ENST00000635776.1:c.2291C>G	ENSP00000490692.1:p.Thr764Ser
ENST00000636194.1:c.2291C>G	ENSP00000490288.1:p.Thr764Ser
ENST00000636759.1:c.*2114C>G	ENSP00000490895.1:n.*2114C>G
ENST00000637968.1:n.2576C>G
ENST00000637988.1:c.2291C>G	ENSP00000490780.1:p.Thr764Ser
ENST00000640036.1:c.2291C>G	ENSP00000491573.1:p.Thr764Ser
ENST00000641575.1:c.2288C>G	ENSP00000492917.1:p.Thr763Ser
ENST00000641603.1:c.2324C>G	ENSP00000492945.1:p.Thr775Ser
ENST00000641996.1:c.*1878C>G	ENSP00000493054.1:n.*1878C>G
ENST00000671940.1:c.*267C>G	ENSP00000500336.1:n.*267C>G
ENST00000673490.1:n.4797C>G
ENST00000674923.1:c.2324C>G MANE Select	ENSP00000501589.1:p.Thr775Ser
ENST00000303395.8:c.2324C>G	ENSP00000303540.4:p.Thr775Ser
ENST00000375405.7:c.2291C>G	ENSP00000364554.3:p.Thr764Ser
ENST00000409050.1:c.2240C>G	ENSP00000386312.1:p.Thr747Ser
ENST00000423058.6:c.2324C>G	ENSP00000407030.2:p.Thr775Ser
NM_001165963.1:c.2324C>G	NP_001159435.1:p.Thr775Ser
NM_001165964.1:c.2240C>G	NP_001159436.1:p.Thr747Ser
NM_001202435.1:c.2324C>G	NP_001189364.1:p.Thr775Ser
NM_006920.4:c.2291C>G , LRG_8t1:c.2291C>G	NP_008851.3:p.Thr764Ser
XM_011511598.1:c.2324C>G	XP_011509900.1:p.Thr775Ser
XM_011511599.1:c.2324C>G	XP_011509901.1:p.Thr775Ser
XM_011511600.1:c.2324C>G	XP_011509902.1:p.Thr775Ser
XM_011511601.1:c.2324C>G	XP_011509903.1:p.Thr775Ser
XM_011511602.1:c.2324C>G	XP_011509904.1:p.Thr775Ser
XM_011511603.1:c.2321C>G	XP_011509905.1:p.Thr774Ser
XM_011511604.1:c.2291C>G	XP_011509906.1:p.Thr764Ser
XM_011511605.1:c.2288C>G	XP_011509907.1:p.Thr763Ser
XM_011511606.1:c.2240C>G	XP_011509908.1:p.Thr747Ser
XM_011511607.1:c.2324C>G	XP_011509909.1:p.Thr775Ser
XR_922981.1:n.2508C>G
NM_001165963.2:c.2324C>G	NP_001159435.1:p.Thr775Ser
NM_001165964.2:c.2240C>G	NP_001159436.1:p.Thr747Ser
NM_001202435.2:c.2324C>G	NP_001189364.1:p.Thr775Ser
NM_001353948.1:c.2324C>G	NP_001340877.1:p.Thr775Ser
NM_001353949.1:c.2291C>G	NP_001340878.1:p.Thr764Ser
NM_001353950.1:c.2291C>G	NP_001340879.1:p.Thr764Ser
NM_001353951.1:c.2291C>G	NP_001340880.1:p.Thr764Ser
NM_001353952.1:c.2291C>G	NP_001340881.1:p.Thr764Ser
NM_001353954.1:c.2288C>G	NP_001340883.1:p.Thr763Ser
NM_001353955.1:c.2288C>G	NP_001340884.1:p.Thr763Ser
NM_001353957.1:c.2240C>G	NP_001340886.1:p.Thr747Ser
NM_001353958.1:c.2240C>G	NP_001340887.1:p.Thr747Ser
NM_001353960.1:c.2237C>G	NP_001340889.1:p.Thr746Ser
NM_001353961.1:c.-135C>G	NP_001340890.1:n.-135C>G
NM_006920.5:c.2291C>G	NP_008851.3:p.Thr764Ser
NR_148667.1:n.2696C>G
XR_001738883.1:n.2710C>G
XR_001738884.1:n.2682C>G
NM_001165963.3:c.2324C>G	NP_001159435.1:p.Thr775Ser
NM_001165964.3:c.2240C>G	NP_001159436.1:p.Thr747Ser
NM_001202435.3:c.2324C>G	NP_001189364.1:p.Thr775Ser
NM_001353948.2:c.2324C>G	NP_001340877.1:p.Thr775Ser
NM_001353949.2:c.2291C>G	NP_001340878.1:p.Thr764Ser
NM_001353950.2:c.2291C>G	NP_001340879.1:p.Thr764Ser
NM_001353951.2:c.2291C>G	NP_001340880.1:p.Thr764Ser
NM_001353952.2:c.2291C>G	NP_001340881.1:p.Thr764Ser
NM_001353954.2:c.2288C>G	NP_001340883.1:p.Thr763Ser
NM_001353955.2:c.2288C>G	NP_001340884.1:p.Thr763Ser
NM_001353957.2:c.2240C>G	NP_001340886.1:p.Thr747Ser
NM_001353958.2:c.2240C>G	NP_001340887.1:p.Thr747Ser
NM_001353960.2:c.2237C>G	NP_001340889.1:p.Thr746Ser
NM_001353961.2:c.-135C>G	NP_001340890.1:n.-135C>G
NM_006920.6:c.2291C>G	NP_008851.3:p.Thr764Ser
NR_148667.2:n.2677C>G
NM_001165963.4:c.2324C>G MANE Select	NP_001159435.1:p.Thr775Ser