Canonical Allele Identifier: CA1304859480

Gene: SCN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166042292C= , CM000664.2:g.166042292C=	GRCh38
NC_000002.11:g.166898802C= , CM000664.1:g.166898802C=	GRCh37
NC_000002.10:g.166607048C=	NCBI36
NG_011906.1:g.36348G= , LRG_8:g.36348G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689288.1:c.*212G=	ENSP00000509637.1:n.*212G=
ENST00000303395.9:c.2176G=	ENSP00000303540.4:p.Glu726=
ENST00000635750.1:c.2143G=	ENSP00000490799.1:p.Glu715=
ENST00000635776.1:c.2143G=	ENSP00000490692.1:p.Glu715=
ENST00000636194.1:c.2143G=	ENSP00000490288.1:p.Glu715=
ENST00000636759.1:c.*1966G=	ENSP00000490895.1:n.*1966G=
ENST00000637968.1:n.2428G=
ENST00000637988.1:c.2143G=	ENSP00000490780.1:p.Glu715=
ENST00000640036.1:c.2143G=	ENSP00000491573.1:p.Glu715=
ENST00000641575.1:c.2140G=	ENSP00000492917.1:p.Glu714=
ENST00000641603.1:c.2176G=	ENSP00000492945.1:p.Glu726=
ENST00000641996.1:c.*1730G=	ENSP00000493054.1:n.*1730G=
ENST00000671940.1:c.*119G=	ENSP00000500336.1:n.*119G=
ENST00000673490.1:n.4649G=
ENST00000674923.1:c.2176G= MANE Select	ENSP00000501589.1:p.Glu726=
ENST00000303395.8:c.2176G=	ENSP00000303540.4:p.Glu726=
ENST00000375405.7:c.2143G=	ENSP00000364554.3:p.Glu715=
ENST00000409050.1:c.2092G=	ENSP00000386312.1:p.Glu698=
ENST00000423058.6:c.2176G=	ENSP00000407030.2:p.Glu726=
NM_001165963.1:c.2176G=	NP_001159435.1:p.Glu726=
NM_001165964.1:c.2092G=	NP_001159436.1:p.Glu698=
NM_001202435.1:c.2176G=	NP_001189364.1:p.Glu726=
NM_006920.4:c.2143G= , LRG_8t1:c.2143G=	NP_008851.3:p.Glu715=
XM_011511598.1:c.2176G=	XP_011509900.1:p.Glu726=
XM_011511599.1:c.2176G=	XP_011509901.1:p.Glu726=
XM_011511600.1:c.2176G=	XP_011509902.1:p.Glu726=
XM_011511601.1:c.2176G=	XP_011509903.1:p.Glu726=
XM_011511602.1:c.2176G=	XP_011509904.1:p.Glu726=
XM_011511603.1:c.2173G=	XP_011509905.1:p.Glu725=
XM_011511604.1:c.2143G=	XP_011509906.1:p.Glu715=
XM_011511605.1:c.2140G=	XP_011509907.1:p.Glu714=
XM_011511606.1:c.2092G=	XP_011509908.1:p.Glu698=
XM_011511607.1:c.2176G=	XP_011509909.1:p.Glu726=
XR_922981.1:n.2360G=
NM_001165963.2:c.2176G=	NP_001159435.1:p.Glu726=
NM_001165964.2:c.2092G=	NP_001159436.1:p.Glu698=
NM_001202435.2:c.2176G=	NP_001189364.1:p.Glu726=
NM_001353948.1:c.2176G=	NP_001340877.1:p.Glu726=
NM_001353949.1:c.2143G=	NP_001340878.1:p.Glu715=
NM_001353950.1:c.2143G=	NP_001340879.1:p.Glu715=
NM_001353951.1:c.2143G=	NP_001340880.1:p.Glu715=
NM_001353952.1:c.2143G=	NP_001340881.1:p.Glu715=
NM_001353954.1:c.2140G=	NP_001340883.1:p.Glu714=
NM_001353955.1:c.2140G=	NP_001340884.1:p.Glu714=
NM_001353957.1:c.2092G=	NP_001340886.1:p.Glu698=
NM_001353958.1:c.2092G=	NP_001340887.1:p.Glu698=
NM_001353960.1:c.2089G=	NP_001340889.1:p.Glu697=
NM_001353961.1:c.-283G=	NP_001340890.1:n.-283G=
NM_006920.5:c.2143G=	NP_008851.3:p.Glu715=
NR_148667.1:n.2548G=
XR_001738883.1:n.2562G=
XR_001738884.1:n.2534G=
NM_001165963.3:c.2176G=	NP_001159435.1:p.Glu726=
NM_001165964.3:c.2092G=	NP_001159436.1:p.Glu698=
NM_001202435.3:c.2176G=	NP_001189364.1:p.Glu726=
NM_001353948.2:c.2176G=	NP_001340877.1:p.Glu726=
NM_001353949.2:c.2143G=	NP_001340878.1:p.Glu715=
NM_001353950.2:c.2143G=	NP_001340879.1:p.Glu715=
NM_001353951.2:c.2143G=	NP_001340880.1:p.Glu715=
NM_001353952.2:c.2143G=	NP_001340881.1:p.Glu715=
NM_001353954.2:c.2140G=	NP_001340883.1:p.Glu714=
NM_001353955.2:c.2140G=	NP_001340884.1:p.Glu714=
NM_001353957.2:c.2092G=	NP_001340886.1:p.Glu698=
NM_001353958.2:c.2092G=	NP_001340887.1:p.Glu698=
NM_001353960.2:c.2089G=	NP_001340889.1:p.Glu697=
NM_001353961.2:c.-283G=	NP_001340890.1:n.-283G=
NM_006920.6:c.2143G=	NP_008851.3:p.Glu715=
NR_148667.2:n.2529G=
NM_001165963.4:c.2176G= MANE Select	NP_001159435.1:p.Glu726=