Canonical Allele Identifier: CA019849

Gene: SCN5A

Linked Data

• ClinVar Variation Id: 68048
• ClinVar RCV Id: RCV000058851 ; RCV000144028 ; RCV001552667 ; RCV003591675 ; RCV002444522
• dbSNP Id: rs199473083
• ExAC: 3:38651314 C / T
• gnomAD v2: 3-38651314-C-T
• gnomAD v4: 3-38609823-C-T
• COSMIC: COSM4117371 ; COSM4117372 ; COSM4117373
• MyVariant Identifiers: chr3:g.38651314C>T (hg19) ; chr3:g.38609823C>T (hg38)
• PubMed: PMID:11901046 ; PMID:15828879 ; PMID:20301690 ; PMID:21840964 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38609823C>T , CM000665.2:g.38609823C>T	GRCh38
NC_000003.11:g.38651314C>T , CM000665.1:g.38651314C>T	GRCh37
NC_000003.10:g.38626318C>T	NCBI36
NG_008934.1:g.44850G>A , LRG_289:g.44850G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.845G>A	ENSP00000333674.7:p.Arg282His
ENST00000333535.9:c.845G>A	ENSP00000328968.4:p.Arg282His
ENST00000413689.6:c.845G>A MANE Plus Clinical	ENSP00000410257.1:p.Arg282His
ENST00000423572.7:c.845G>A MANE Select	ENSP00000398266.2:p.Arg282His
ENST00000333535.8:c.845G>A	ENSP00000328968.4:p.Arg282His
ENST00000413689.5:c.845G>A	ENSP00000410257.1:p.Arg282His
ENST00000414099.6:c.845G>A	ENSP00000398962.2:p.Arg282His
ENST00000423572.6:c.845G>A	ENSP00000398266.2:p.Arg282His
ENST00000425664.5:c.845G>A	ENSP00000416634.1:p.Arg282His
ENST00000449557.6:c.845G>A	ENSP00000413996.2:p.Arg282His
ENST00000450102.6:c.845G>A	ENSP00000403355.2:p.Arg282His
ENST00000451551.6:c.845G>A	ENSP00000388797.2:p.Arg282His
ENST00000455624.6:c.845G>A	ENSP00000399524.2:p.Arg282His
NM_000335.4:c.845G>A , LRG_289t2:c.845G>A	NP_000326.2:p.Arg282His
NM_001099404.1:c.845G>A , LRG_289t3:c.845G>A	NP_001092874.1:p.Arg282His
NM_001099405.1:c.845G>A	NP_001092875.1:p.Arg282His
NM_001160160.1:c.845G>A	NP_001153632.1:p.Arg282His
NM_001160161.1:c.845G>A	NP_001153633.1:p.Arg282His
NM_198056.2:c.845G>A , LRG_289t1:c.845G>A	NP_932173.1:p.Arg282His
XM_006713282.2:c.845G>A	XP_006713345.1:p.Arg282His
XM_011533991.1:c.845G>A	XP_011532293.1:p.Arg282His
XM_011533992.1:c.716G>A	XP_011532294.1:p.Arg239His
NM_001354701.1:c.845G>A	NP_001341630.1:p.Arg282His
XM_011533991.2:c.845G>A	XP_011532293.1:p.Arg282His
XM_017007017.1:c.845G>A	XP_016862506.1:p.Arg282His
NM_000335.5:c.845G>A MANE Select	NP_000326.2:p.Arg282His
NM_001160160.2:c.845G>A	NP_001153632.1:p.Arg282His
NM_001354701.2:c.845G>A	NP_001341630.1:p.Arg282His
NM_001099404.2:c.845G>A MANE Plus Clinical	NP_001092874.1:p.Arg282His
NM_001099405.2:c.845G>A	NP_001092875.1:p.Arg282His
NM_001160161.2:c.845G>A	NP_001153633.1:p.Arg282His
NM_198056.3:c.845G>A	NP_932173.1:p.Arg282His