Canonical Allele Identifier: CA1139655765

Gene: SCN5A

Linked Data

• ClinVar Variation Id: 923735
• ClinVar RCV Id: RCV001843222 ; RCV003541285

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38603929_38603930delinsCA , CM000665.2:g.38603929_38603930delinsCA	GRCh38
NC_000003.11:g.38645420_38645421delinsCA , CM000665.1:g.38645420_38645421delinsCA	GRCh37
NC_000003.10:g.38620424_38620425delinsCA	NCBI36
NG_008934.1:g.50743_50744delinsTG , LRG_289:g.50743_50744delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.1672_1673delinsTG	ENSP00000333674.7:p.His558Cys
ENST00000333535.9:c.1672_1673delinsTG	ENSP00000328968.4:p.His558Cys
ENST00000413689.6:c.1672_1673delinsTG MANE Plus Clinical	ENSP00000410257.1:p.His558Cys
ENST00000423572.7:c.1672_1673delinsTG MANE Select	ENSP00000398266.2:p.His558Cys
ENST00000333535.8:c.1672_1673delinsTG	ENSP00000328968.4:p.His558Cys
ENST00000413689.5:c.1672_1673delinsTG	ENSP00000410257.1:p.His558Cys
ENST00000414099.6:c.1672_1673delinsTG	ENSP00000398962.2:p.His558Cys
ENST00000423572.6:c.1672_1673delinsTG	ENSP00000398266.2:p.His558Cys
ENST00000425664.5:c.1672_1673delinsTG	ENSP00000416634.1:p.His558Cys
ENST00000449557.6:c.1672_1673delinsTG	ENSP00000413996.2:p.His558Cys
ENST00000450102.6:c.1672_1673delinsTG	ENSP00000403355.2:p.His558Cys
ENST00000451551.6:c.1672_1673delinsTG	ENSP00000388797.2:p.His558Cys
ENST00000455624.6:c.1672_1673delinsTG	ENSP00000399524.2:p.His558Cys
NM_000335.4:c.1672_1673delinsTG , LRG_289t2:c.1672_1673delinsTG	NP_000326.2:p.His558Cys
NM_001099404.1:c.1672_1673delinsTG , LRG_289t3:c.1672_1673delinsTG	NP_001092874.1:p.His558Cys
NM_001099405.1:c.1672_1673delinsTG	NP_001092875.1:p.His558Cys
NM_001160160.1:c.1672_1673delinsTG	NP_001153632.1:p.His558Cys
NM_001160161.1:c.1672_1673delinsTG	NP_001153633.1:p.His558Cys
NM_198056.2:c.1672_1673delinsTG , LRG_289t1:c.1672_1673delinsTG	NP_932173.1:p.His558Cys
XM_006713282.2:c.1672_1673delinsTG	XP_006713345.1:p.His558Cys
XM_011533991.1:c.1672_1673delinsTG	XP_011532293.1:p.His558Cys
XM_011533992.1:c.1543_1544delinsTG	XP_011532294.1:p.His515Cys
NM_001354701.1:c.1672_1673delinsTG	NP_001341630.1:p.His558Cys
XM_011533991.2:c.1672_1673delinsTG	XP_011532293.1:p.His558Cys
XM_017007017.1:c.1672_1673delinsTG	XP_016862506.1:p.His558Cys
NM_000335.5:c.1672_1673delinsTG MANE Select	NP_000326.2:p.His558Cys
NM_001160160.2:c.1672_1673delinsTG	NP_001153632.1:p.His558Cys
NM_001354701.2:c.1672_1673delinsTG	NP_001341630.1:p.His558Cys
NM_001099404.2:c.1672_1673delinsTG MANE Plus Clinical	NP_001092874.1:p.His558Cys
NM_001099405.2:c.1672_1673delinsTG	NP_001092875.1:p.His558Cys
NM_001160161.2:c.1672_1673delinsTG	NP_001153633.1:p.His558Cys
NM_198056.3:c.1672_1673delinsTG	NP_932173.1:p.His558Cys