Canonical Allele Identifier: CA1358585878

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38605897_38605904delinsGCACCTAC , CM000665.2:g.38605897_38605904delinsGCACCTAC	GRCh38
NC_000003.11:g.38647388_38647395delinsGCACCTAC , CM000665.1:g.38647388_38647395delinsGCACCTAC	GRCh37
NC_000003.10:g.38622392_38622399delinsGCACCTAC	NCBI36
NG_008934.1:g.48769_48776delinsGTAGGTGC , LRG_289:g.48769_48776delinsGTAGGTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000327956.7:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000333674.7:n.1338+47_1338+54delinsGTAGGTGC
ENST00000333535.9:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000328968.4:n.1338+47_1338+54delinsGTAGGTGC
ENST00000413689.6:c.1338+47_1338+54delinsGTAGGTGC MANE Plus Clinical	ENSP00000410257.1:n.1338+47_1338+54delinsGTAGGTGC
ENST00000423572.7:c.1338+47_1338+54delinsGTAGGTGC MANE Select	ENSP00000398266.2:n.1338+47_1338+54delinsGTAGGTGC
ENST00000333535.8:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000328968.4:n.1338+47_1338+54delinsGTAGGTGC
ENST00000413689.5:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000410257.1:n.1338+47_1338+54delinsGTAGGTGC
ENST00000414099.6:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000398962.2:n.1338+47_1338+54delinsGTAGGTGC
ENST00000423572.6:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000398266.2:n.1338+47_1338+54delinsGTAGGTGC
ENST00000425664.5:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000416634.1:n.1338+47_1338+54delinsGTAGGTGC
ENST00000449557.6:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000413996.2:n.1338+47_1338+54delinsGTAGGTGC
ENST00000450102.6:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000403355.2:n.1338+47_1338+54delinsGTAGGTGC
ENST00000451551.6:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000388797.2:n.1338+47_1338+54delinsGTAGGTGC
ENST00000455624.6:c.1338+47_1338+54delinsGTAGGTGC	ENSP00000399524.2:n.1338+47_1338+54delinsGTAGGTGC
NM_000335.4:c.1338+47_1338+54delinsGTAGGTGC , LRG_289t2:c.1338+47_1338+54delinsGTAGGTGC	NP_000326.2:n.1338+47_1338+54delinsGTAGGTGC
NM_001099404.1:c.1338+47_1338+54delinsGTAGGTGC , LRG_289t3:c.1338+47_1338+54delinsGTAGGTGC	NP_001092874.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001099405.1:c.1338+47_1338+54delinsGTAGGTGC	NP_001092875.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001160160.1:c.1338+47_1338+54delinsGTAGGTGC	NP_001153632.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001160161.1:c.1338+47_1338+54delinsGTAGGTGC	NP_001153633.1:n.1338+47_1338+54delinsGTAGGTGC
NM_198056.2:c.1338+47_1338+54delinsGTAGGTGC , LRG_289t1:c.1338+47_1338+54delinsGTAGGTGC	NP_932173.1:n.1338+47_1338+54delinsGTAGGTGC
XM_006713282.2:c.1338+47_1338+54delinsGTAGGTGC	XP_006713345.1:n.1338+47_1338+54delinsGTAGGTGC
XM_011533991.1:c.1338+47_1338+54delinsGTAGGTGC	XP_011532293.1:n.1338+47_1338+54delinsGTAGGTGC
XM_011533992.1:c.1209+47_1209+54delinsGTAGGTGC	XP_011532294.1:n.1209+47_1209+54delinsGTAGGTGC
NM_001354701.1:c.1338+47_1338+54delinsGTAGGTGC	NP_001341630.1:n.1338+47_1338+54delinsGTAGGTGC
XM_011533991.2:c.1338+47_1338+54delinsGTAGGTGC	XP_011532293.1:n.1338+47_1338+54delinsGTAGGTGC
XM_017007017.1:c.1338+47_1338+54delinsGTAGGTGC	XP_016862506.1:n.1338+47_1338+54delinsGTAGGTGC
NM_000335.5:c.1338+47_1338+54delinsGTAGGTGC MANE Select	NP_000326.2:n.1338+47_1338+54delinsGTAGGTGC
NM_001160160.2:c.1338+47_1338+54delinsGTAGGTGC	NP_001153632.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001354701.2:c.1338+47_1338+54delinsGTAGGTGC	NP_001341630.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001099404.2:c.1338+47_1338+54delinsGTAGGTGC MANE Plus Clinical	NP_001092874.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001099405.2:c.1338+47_1338+54delinsGTAGGTGC	NP_001092875.1:n.1338+47_1338+54delinsGTAGGTGC
NM_001160161.2:c.1338+47_1338+54delinsGTAGGTGC	NP_001153633.1:n.1338+47_1338+54delinsGTAGGTGC
NM_198056.3:c.1338+47_1338+54delinsGTAGGTGC	NP_932173.1:n.1338+47_1338+54delinsGTAGGTGC