Canonical Allele Identifier: CA2586965777

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551005_38551007del , CM000665.2:g.38551005_38551007del	GRCh38
NC_000003.11:g.38592496_38592498del , CM000665.1:g.38592496_38592498del	GRCh37
NC_000003.10:g.38567500_38567502del	NCBI36
NG_008934.1:g.103669_103671del , LRG_289:g.103669_103671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.5365_5367del	ENSP00000333674.7:p.Asp1789del
ENST00000333535.9:c.5368_5370del	ENSP00000328968.4:p.Asp1790del
ENST00000413689.6:c.5368_5370del MANE Plus Clinical	ENSP00000410257.1:p.Asp1790del
ENST00000423572.7:c.5365_5367del MANE Select	ENSP00000398266.2:p.Asp1789del
ENST00000333535.8:c.5368_5370del	ENSP00000328968.4:p.Asp1790del
ENST00000413689.5:c.5368_5370del	ENSP00000410257.1:p.Asp1790del
ENST00000414099.6:c.5314_5316del	ENSP00000398962.2:p.Asp1772del
ENST00000423572.6:c.5365_5367del	ENSP00000398266.2:p.Asp1789del
ENST00000425664.5:c.5314_5316del	ENSP00000416634.1:p.Asp1772del
ENST00000449557.6:c.5206_5208del	ENSP00000413996.2:p.Asp1736del
ENST00000450102.6:c.5206_5208del	ENSP00000403355.2:p.Asp1736del
ENST00000451551.6:c.5206_5208del	ENSP00000388797.2:p.Asp1736del
ENST00000455624.6:c.5269_5271del	ENSP00000399524.2:p.Asp1757del
NM_000335.4:c.5365_5367del , LRG_289t2:c.5365_5367del	NP_000326.2:p.Asp1789del
NM_001099404.1:c.5368_5370del , LRG_289t3:c.5368_5370del	NP_001092874.1:p.Asp1790del
NM_001099405.1:c.5314_5316del	NP_001092875.1:p.Asp1772del
NM_001160160.1:c.5269_5271del	NP_001153632.1:p.Asp1757del
NM_001160161.1:c.5206_5208del	NP_001153633.1:p.Asp1736del
NM_198056.2:c.5368_5370del , LRG_289t1:c.5368_5370del	NP_932173.1:p.Asp1790del
XM_006713282.2:c.5368_5370del	XP_006713345.1:p.Asp1790del
XM_011533991.1:c.5365_5367del	XP_011532293.1:p.Asp1789del
XM_011533992.1:c.5239_5241del	XP_011532294.1:p.Asp1747del
NM_001354701.1:c.5311_5313del	NP_001341630.1:p.Asp1771del
XM_011533991.2:c.5365_5367del	XP_011532293.1:p.Asp1789del
XM_017007017.1:c.5206_5208del	XP_016862506.1:p.Asp1736del
NM_000335.5:c.5365_5367del MANE Select	NP_000326.2:p.Asp1789del
NM_001160160.2:c.5269_5271del	NP_001153632.1:p.Asp1757del
NM_001354701.2:c.5311_5313del	NP_001341630.1:p.Asp1771del
NM_001099404.2:c.5368_5370del MANE Plus Clinical	NP_001092874.1:p.Asp1790del
NM_001099405.2:c.5314_5316del	NP_001092875.1:p.Asp1772del
NM_001160161.2:c.5206_5208del	NP_001153633.1:p.Asp1736del
NM_198056.3:c.5368_5370del	NP_932173.1:p.Asp1790del