Canonical Allele Identifier: CA1304837877

Gene: SCN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165991370_165991372delinsTAG , CM000664.2:g.165991370_165991372delinsTAG	GRCh38
NC_000002.11:g.166847880_166847882delinsTAG , CM000664.1:g.166847880_166847882delinsTAG	GRCh37
NC_000002.10:g.166556126_166556128delinsTAG	NCBI36
NG_011906.1:g.87268_87270delinsCTA , LRG_8:g.87268_87270delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689288.1:c.*3939_*3941delinsCTA	ENSP00000509637.1:n.*3939_*3941delinsCTA
ENST00000303395.9:c.5903_5905delinsCTA	ENSP00000303540.4:p.Ser1968=
ENST00000635750.1:c.5870_5872delinsCTA	ENSP00000490799.1:p.Ser1957=
ENST00000635776.1:c.*2736_*2738delinsCTA	ENSP00000490692.1:n.*2736_*2738delinsCTA
ENST00000636194.1:c.*3396_*3398delinsCTA	ENSP00000490288.1:n.*3396_*3398delinsCTA
ENST00000637038.1:c.2765_2767delinsCTA
ENST00000637988.1:c.5870_5872delinsCTA	ENSP00000490780.1:p.Ser1957=
ENST00000640036.1:c.5870_5872delinsCTA	ENSP00000491573.1:p.Ser1957=
ENST00000641575.1:c.5867_5869delinsCTA	ENSP00000492917.1:p.Ser1956=
ENST00000641603.1:c.5621_5623delinsCTA	ENSP00000492945.1:p.Ser1874=
ENST00000641996.1:c.*5457_*5459delinsCTA	ENSP00000493054.1:n.*5457_*5459delinsCTA
ENST00000671940.1:c.*3846_*3848delinsCTA	ENSP00000500336.1:n.*3846_*3848delinsCTA
ENST00000673490.1:n.8376_8378delinsCTA
ENST00000674923.1:c.5903_5905delinsCTA MANE Select	ENSP00000501589.1:p.Ser1968=
ENST00000303395.8:c.5903_5905delinsCTA	ENSP00000303540.4:p.Ser1968=
ENST00000375405.7:c.5870_5872delinsCTA	ENSP00000364554.3:p.Ser1957=
ENST00000409050.1:c.5819_5821delinsCTA	ENSP00000386312.1:p.Ser1940=
ENST00000423058.6:c.5903_5905delinsCTA	ENSP00000407030.2:p.Ser1968=
NM_001165963.1:c.5903_5905delinsCTA	NP_001159435.1:p.Ser1968=
NM_001165964.1:c.5819_5821delinsCTA	NP_001159436.1:p.Ser1940=
NM_001202435.1:c.5903_5905delinsCTA	NP_001189364.1:p.Ser1968=
NM_006920.4:c.5870_5872delinsCTA , LRG_8t1:c.5870_5872delinsCTA	NP_008851.3:p.Ser1957=
NR_110598.1:n.176-24243_176-24241delinsTAG
XM_011511598.1:c.5903_5905delinsCTA	XP_011509900.1:p.Ser1968=
XM_011511599.1:c.5903_5905delinsCTA	XP_011509901.1:p.Ser1968=
XM_011511600.1:c.5903_5905delinsCTA	XP_011509902.1:p.Ser1968=
XM_011511601.1:c.5903_5905delinsCTA	XP_011509903.1:p.Ser1968=
XM_011511602.1:c.5903_5905delinsCTA	XP_011509904.1:p.Ser1968=
XM_011511603.1:c.5900_5902delinsCTA	XP_011509905.1:p.Ser1967=
XM_011511604.1:c.5870_5872delinsCTA	XP_011509906.1:p.Ser1957=
XM_011511605.1:c.5867_5869delinsCTA	XP_011509907.1:p.Ser1956=
XM_011511606.1:c.5819_5821delinsCTA	XP_011509908.1:p.Ser1940=
XM_011511607.1:c.5621_5623delinsCTA	XP_011509909.1:p.Ser1874=
NM_001165963.2:c.5903_5905delinsCTA	NP_001159435.1:p.Ser1968=
NM_001165964.2:c.5819_5821delinsCTA	NP_001159436.1:p.Ser1940=
NM_001202435.2:c.5903_5905delinsCTA	NP_001189364.1:p.Ser1968=
NM_001353948.1:c.5903_5905delinsCTA	NP_001340877.1:p.Ser1968=
NM_001353949.1:c.5870_5872delinsCTA	NP_001340878.1:p.Ser1957=
NM_001353950.1:c.5870_5872delinsCTA	NP_001340879.1:p.Ser1957=
NM_001353951.1:c.5870_5872delinsCTA	NP_001340880.1:p.Ser1957=
NM_001353952.1:c.5870_5872delinsCTA	NP_001340881.1:p.Ser1957=
NM_001353954.1:c.5867_5869delinsCTA	NP_001340883.1:p.Ser1956=
NM_001353955.1:c.5867_5869delinsCTA	NP_001340884.1:p.Ser1956=
NM_001353957.1:c.5819_5821delinsCTA	NP_001340886.1:p.Ser1940=
NM_001353958.1:c.5819_5821delinsCTA	NP_001340887.1:p.Ser1940=
NM_001353960.1:c.5816_5818delinsCTA	NP_001340889.1:p.Ser1939=
NM_001353961.1:c.3461_3463delinsCTA	NP_001340890.1:p.Ser1154=
NM_006920.5:c.5870_5872delinsCTA	NP_008851.3:p.Ser1957=
NR_148667.1:n.6339_6341delinsCTA
XR_001738883.1:n.6353_6355delinsCTA
XR_001738884.1:n.6325_6327delinsCTA
NM_001165963.3:c.5903_5905delinsCTA	NP_001159435.1:p.Ser1968=
NM_001165964.3:c.5819_5821delinsCTA	NP_001159436.1:p.Ser1940=
NM_001202435.3:c.5903_5905delinsCTA	NP_001189364.1:p.Ser1968=
NM_001353948.2:c.5903_5905delinsCTA	NP_001340877.1:p.Ser1968=
NM_001353949.2:c.5870_5872delinsCTA	NP_001340878.1:p.Ser1957=
NM_001353950.2:c.5870_5872delinsCTA	NP_001340879.1:p.Ser1957=
NM_001353951.2:c.5870_5872delinsCTA	NP_001340880.1:p.Ser1957=
NM_001353952.2:c.5870_5872delinsCTA	NP_001340881.1:p.Ser1957=
NM_001353954.2:c.5867_5869delinsCTA	NP_001340883.1:p.Ser1956=
NM_001353955.2:c.5867_5869delinsCTA	NP_001340884.1:p.Ser1956=
NM_001353957.2:c.5819_5821delinsCTA	NP_001340886.1:p.Ser1940=
NM_001353958.2:c.5819_5821delinsCTA	NP_001340887.1:p.Ser1940=
NM_001353960.2:c.5816_5818delinsCTA	NP_001340889.1:p.Ser1939=
NM_001353961.2:c.3461_3463delinsCTA	NP_001340890.1:p.Ser1154=
NM_006920.6:c.5870_5872delinsCTA	NP_008851.3:p.Ser1957=
NR_148667.2:n.6320_6322delinsCTA
NM_001165963.4:c.5903_5905delinsCTA MANE Select	NP_001159435.1:p.Ser1968=