Canonical Allele Identifier: CA352143725

Gene: SCN5A

Linked Data

• ClinVar Variation Id: 1411956
• ClinVar RCV Id: RCV001923003
• dbSNP Id: rs2125830627
• MyVariant Identifiers: chr3:g.38595845C>A (hg19) ; chr3:g.38554354C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38554354C>A , CM000665.2:g.38554354C>A	GRCh38
NC_000003.11:g.38595845C>A , CM000665.1:g.38595845C>A	GRCh37
NC_000003.10:g.38570849C>A	NCBI36
NG_008934.1:g.100319G>T , LRG_289:g.100319G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4735G>T	ENSP00000333674.7:p.Ala1579Ser
ENST00000333535.9:c.4738G>T	ENSP00000328968.4:p.Ala1580Ser
ENST00000413689.6:c.4738G>T MANE Plus Clinical	ENSP00000410257.1:p.Ala1580Ser
ENST00000423572.7:c.4735G>T MANE Select	ENSP00000398266.2:p.Ala1579Ser
ENST00000333535.8:c.4738G>T	ENSP00000328968.4:p.Ala1580Ser
ENST00000413689.5:c.4738G>T	ENSP00000410257.1:p.Ala1580Ser
ENST00000414099.6:c.4684G>T	ENSP00000398962.2:p.Ala1562Ser
ENST00000423572.6:c.4735G>T	ENSP00000398266.2:p.Ala1579Ser
ENST00000425664.5:c.4684G>T	ENSP00000416634.1:p.Ala1562Ser
ENST00000449557.6:c.4576G>T	ENSP00000413996.2:p.Ala1526Ser
ENST00000450102.6:c.4576G>T	ENSP00000403355.2:p.Ala1526Ser
ENST00000451551.6:c.4576G>T	ENSP00000388797.2:p.Ala1526Ser
ENST00000455624.6:c.4714+21G>T	ENSP00000399524.2:n.4714+21G>T
ENST00000464652.1:n.196G>T
NM_000335.4:c.4735G>T , LRG_289t2:c.4735G>T	NP_000326.2:p.Ala1579Ser
NM_001099404.1:c.4738G>T , LRG_289t3:c.4738G>T	NP_001092874.1:p.Ala1580Ser
NM_001099405.1:c.4684G>T	NP_001092875.1:p.Ala1562Ser
NM_001160160.1:c.4714+21G>T	NP_001153632.1:n.4714+21G>T
NM_001160161.1:c.4576G>T	NP_001153633.1:p.Ala1526Ser
NM_198056.2:c.4738G>T , LRG_289t1:c.4738G>T	NP_932173.1:p.Ala1580Ser
XM_006713282.2:c.4738G>T	XP_006713345.1:p.Ala1580Ser
XM_011533991.1:c.4735G>T	XP_011532293.1:p.Ala1579Ser
XM_011533992.1:c.4609G>T	XP_011532294.1:p.Ala1537Ser
NM_001354701.1:c.4681G>T	NP_001341630.1:p.Ala1561Ser
XM_011533991.2:c.4735G>T	XP_011532293.1:p.Ala1579Ser
XM_017007017.1:c.4576G>T	XP_016862506.1:p.Ala1526Ser
NM_000335.5:c.4735G>T MANE Select	NP_000326.2:p.Ala1579Ser
NM_001160160.2:c.4714+21G>T	NP_001153632.1:n.4714+21G>T
NM_001354701.2:c.4681G>T	NP_001341630.1:p.Ala1561Ser
NM_001099404.2:c.4738G>T MANE Plus Clinical	NP_001092874.1:p.Ala1580Ser
NM_001099405.2:c.4684G>T	NP_001092875.1:p.Ala1562Ser
NM_001160161.2:c.4576G>T	NP_001153633.1:p.Ala1526Ser
NM_198056.3:c.4738G>T	NP_932173.1:p.Ala1580Ser