Canonical Allele Identifier: CA1358563453

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38556481_38556482delinsAT , CM000665.2:g.38556481_38556482delinsAT	GRCh38
NC_000003.11:g.38597972_38597973delinsAT , CM000665.1:g.38597972_38597973delinsAT	GRCh37
NC_000003.10:g.38572976_38572977delinsAT	NCBI36
NG_008934.1:g.98191_98192delinsAT , LRG_289:g.98191_98192delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000327956.7:c.4393_4394delinsAT	ENSP00000333674.7:p.Ile1465=
ENST00000333535.9:c.4396_4397delinsAT	ENSP00000328968.4:p.Ile1466=
ENST00000413689.6:c.4396_4397delinsAT MANE Plus Clinical	ENSP00000410257.1:p.Ile1466=
ENST00000423572.7:c.4393_4394delinsAT MANE Select	ENSP00000398266.2:p.Ile1465=
ENST00000333535.8:c.4396_4397delinsAT	ENSP00000328968.4:p.Ile1466=
ENST00000413689.5:c.4396_4397delinsAT	ENSP00000410257.1:p.Ile1466=
ENST00000414099.6:c.4342_4343delinsAT	ENSP00000398962.2:p.Ile1448=
ENST00000423572.6:c.4393_4394delinsAT	ENSP00000398266.2:p.Ile1465=
ENST00000425664.5:c.4342_4343delinsAT	ENSP00000416634.1:p.Ile1448=
ENST00000449557.6:c.4234_4235delinsAT	ENSP00000413996.2:p.Ile1412=
ENST00000450102.6:c.4234_4235delinsAT	ENSP00000403355.2:p.Ile1412=
ENST00000451551.6:c.4234_4235delinsAT	ENSP00000388797.2:p.Ile1412=
ENST00000455624.6:c.4393_4394delinsAT	ENSP00000399524.2:p.Ile1465=
NM_000335.4:c.4393_4394delinsAT , LRG_289t2:c.4393_4394delinsAT	NP_000326.2:p.Ile1465=
NM_001099404.1:c.4396_4397delinsAT , LRG_289t3:c.4396_4397delinsAT	NP_001092874.1:p.Ile1466=
NM_001099405.1:c.4342_4343delinsAT	NP_001092875.1:p.Ile1448=
NM_001160160.1:c.4393_4394delinsAT	NP_001153632.1:p.Ile1465=
NM_001160161.1:c.4234_4235delinsAT	NP_001153633.1:p.Ile1412=
NM_198056.2:c.4396_4397delinsAT , LRG_289t1:c.4396_4397delinsAT	NP_932173.1:p.Ile1466=
XM_006713282.2:c.4396_4397delinsAT	XP_006713345.1:p.Ile1466=
XM_011533991.1:c.4393_4394delinsAT	XP_011532293.1:p.Ile1465=
XM_011533992.1:c.4267_4268delinsAT	XP_011532294.1:p.Ile1423=
NM_001354701.1:c.4339_4340delinsAT	NP_001341630.1:p.Ile1447=
XM_011533991.2:c.4393_4394delinsAT	XP_011532293.1:p.Ile1465=
XM_017007017.1:c.4234_4235delinsAT	XP_016862506.1:p.Ile1412=
NM_000335.5:c.4393_4394delinsAT MANE Select	NP_000326.2:p.Ile1465=
NM_001160160.2:c.4393_4394delinsAT	NP_001153632.1:p.Ile1465=
NM_001354701.2:c.4339_4340delinsAT	NP_001341630.1:p.Ile1447=
NM_001099404.2:c.4396_4397delinsAT MANE Plus Clinical	NP_001092874.1:p.Ile1466=
NM_001099405.2:c.4342_4343delinsAT	NP_001092875.1:p.Ile1448=
NM_001160161.2:c.4234_4235delinsAT	NP_001153633.1:p.Ile1412=
NM_198056.3:c.4396_4397delinsAT	NP_932173.1:p.Ile1466=