Canonical Allele Identifier: CA429976192

Gene: SCN1A

Linked Data

• MyVariant Identifiers: chr2:g.166897822A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166041312A>G , CM000664.2:g.166041312A>G	GRCh38
NC_000002.11:g.166897822A>G , CM000664.1:g.166897822A>G	GRCh37
NC_000002.10:g.166606068A>G	NCBI36
NG_011906.1:g.37328T>C , LRG_8:g.37328T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689288.1:c.*370T>C	ENSP00000509637.1:n.*370T>C
ENST00000303395.9:c.2334T>C	ENSP00000303540.4:p.Ile778=
ENST00000635750.1:c.2301T>C	ENSP00000490799.1:p.Ile767=
ENST00000635776.1:c.2301T>C	ENSP00000490692.1:p.Ile767=
ENST00000636194.1:c.2301T>C	ENSP00000490288.1:p.Ile767=
ENST00000636759.1:c.*2124T>C	ENSP00000490895.1:n.*2124T>C
ENST00000637968.1:n.2586T>C
ENST00000637988.1:c.2301T>C	ENSP00000490780.1:p.Ile767=
ENST00000640036.1:c.2301T>C	ENSP00000491573.1:p.Ile767=
ENST00000641575.1:c.2298T>C	ENSP00000492917.1:p.Ile766=
ENST00000641603.1:c.2334T>C	ENSP00000492945.1:p.Ile778=
ENST00000641996.1:c.*1888T>C	ENSP00000493054.1:n.*1888T>C
ENST00000671940.1:c.*277T>C	ENSP00000500336.1:n.*277T>C
ENST00000673490.1:n.4807T>C
ENST00000674923.1:c.2334T>C MANE Select	ENSP00000501589.1:p.Ile778=
ENST00000303395.8:c.2334T>C	ENSP00000303540.4:p.Ile778=
ENST00000375405.7:c.2301T>C	ENSP00000364554.3:p.Ile767=
ENST00000409050.1:c.2250T>C	ENSP00000386312.1:p.Ile750=
ENST00000423058.6:c.2334T>C	ENSP00000407030.2:p.Ile778=
NM_001165963.1:c.2334T>C	NP_001159435.1:p.Ile778=
NM_001165964.1:c.2250T>C	NP_001159436.1:p.Ile750=
NM_001202435.1:c.2334T>C	NP_001189364.1:p.Ile778=
NM_006920.4:c.2301T>C , LRG_8t1:c.2301T>C	NP_008851.3:p.Ile767=
XM_011511598.1:c.2334T>C	XP_011509900.1:p.Ile778=
XM_011511599.1:c.2334T>C	XP_011509901.1:p.Ile778=
XM_011511600.1:c.2334T>C	XP_011509902.1:p.Ile778=
XM_011511601.1:c.2334T>C	XP_011509903.1:p.Ile778=
XM_011511602.1:c.2334T>C	XP_011509904.1:p.Ile778=
XM_011511603.1:c.2331T>C	XP_011509905.1:p.Ile777=
XM_011511604.1:c.2301T>C	XP_011509906.1:p.Ile767=
XM_011511605.1:c.2298T>C	XP_011509907.1:p.Ile766=
XM_011511606.1:c.2250T>C	XP_011509908.1:p.Ile750=
XM_011511607.1:c.2334T>C	XP_011509909.1:p.Ile778=
XR_922981.1:n.2518T>C
NM_001165963.2:c.2334T>C	NP_001159435.1:p.Ile778=
NM_001165964.2:c.2250T>C	NP_001159436.1:p.Ile750=
NM_001202435.2:c.2334T>C	NP_001189364.1:p.Ile778=
NM_001353948.1:c.2334T>C	NP_001340877.1:p.Ile778=
NM_001353949.1:c.2301T>C	NP_001340878.1:p.Ile767=
NM_001353950.1:c.2301T>C	NP_001340879.1:p.Ile767=
NM_001353951.1:c.2301T>C	NP_001340880.1:p.Ile767=
NM_001353952.1:c.2301T>C	NP_001340881.1:p.Ile767=
NM_001353954.1:c.2298T>C	NP_001340883.1:p.Ile766=
NM_001353955.1:c.2298T>C	NP_001340884.1:p.Ile766=
NM_001353957.1:c.2250T>C	NP_001340886.1:p.Ile750=
NM_001353958.1:c.2250T>C	NP_001340887.1:p.Ile750=
NM_001353960.1:c.2247T>C	NP_001340889.1:p.Ile749=
NM_001353961.1:c.-125T>C	NP_001340890.1:n.-125T>C
NM_006920.5:c.2301T>C	NP_008851.3:p.Ile767=
NR_148667.1:n.2706T>C
XR_001738883.1:n.2720T>C
XR_001738884.1:n.2692T>C
NM_001165963.3:c.2334T>C	NP_001159435.1:p.Ile778=
NM_001165964.3:c.2250T>C	NP_001159436.1:p.Ile750=
NM_001202435.3:c.2334T>C	NP_001189364.1:p.Ile778=
NM_001353948.2:c.2334T>C	NP_001340877.1:p.Ile778=
NM_001353949.2:c.2301T>C	NP_001340878.1:p.Ile767=
NM_001353950.2:c.2301T>C	NP_001340879.1:p.Ile767=
NM_001353951.2:c.2301T>C	NP_001340880.1:p.Ile767=
NM_001353952.2:c.2301T>C	NP_001340881.1:p.Ile767=
NM_001353954.2:c.2298T>C	NP_001340883.1:p.Ile766=
NM_001353955.2:c.2298T>C	NP_001340884.1:p.Ile766=
NM_001353957.2:c.2250T>C	NP_001340886.1:p.Ile750=
NM_001353958.2:c.2250T>C	NP_001340887.1:p.Ile750=
NM_001353960.2:c.2247T>C	NP_001340889.1:p.Ile749=
NM_001353961.2:c.-125T>C	NP_001340890.1:n.-125T>C
NM_006920.6:c.2301T>C	NP_008851.3:p.Ile767=
NR_148667.2:n.2687T>C
NM_001165963.4:c.2334T>C MANE Select	NP_001159435.1:p.Ile778=