Canonical Allele Identifier: CA019280
Gene: SCN5A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9389
dbSNP Id: rs137854610

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38550895C>T , CM000665.2:g.38550895C>T GRCh38
NC_000003.11:g.38592386C>T , CM000665.1:g.38592386C>T GRCh37
NC_000003.10:g.38567390C>T NCBI36
NG_008934.1:g.103778G>A , LRG_289:g.103778G>A

Transcript Alleles

HGVS Amino-acid change
NM_000335.4:c.5474G>A , LRG_289t2:c.5474G>A NP_000326.2:p.Arg1825His
NM_001099404.1:c.5477G>A , LRG_289t3:c.5477G>A NP_001092874.1:p.Arg1826His
NM_001099405.1:c.5423G>A VV NP_001092875.1:p.Arg1808His
NM_001160160.1:c.5378G>A VV NP_001153632.1:p.Arg1793His
NM_001160161.1:c.5315G>A VV NP_001153633.1:p.Arg1772His
NM_198056.2:c.5477G>A , LRG_289t1:c.5477G>A NP_932173.1:p.Arg1826His
XM_006713282.2:c.5477G>A XP_006713345.1:p.Arg1826His
XM_011533991.1:c.5474G>A XP_011532293.1:p.Arg1825His
XM_011533992.1:c.5348G>A XP_011532294.1:p.Arg1783His
NM_001354701.1:c.5420G>A VV NP_001341630.1:p.Arg1807His
XM_011533991.2:c.5474G>A XP_011532293.1:p.Arg1825His
XM_017007017.1:c.5315G>A XP_016862506.1:p.Arg1772His
ENST00000333535.8:c.5477G>A ENSP00000328968.4:p.Arg1826His
ENST00000413689.5:c.5477G>A ENSP00000410257.1:p.Arg1826His
ENST00000414099.6:c.5423G>A ENSP00000398962.2:p.Arg1808His
ENST00000423572.6:c.5474G>A ENSP00000398266.2:p.Arg1825His
ENST00000425664.5:c.5423G>A ENSP00000416634.1:p.Arg1808His
ENST00000449557.6:c.5315G>A ENSP00000413996.2:p.Arg1772His
ENST00000450102.6:c.5315G>A ENSP00000403355.2:p.Arg1772His
ENST00000451551.6:c.5315G>A ENSP00000388797.2:p.Arg1772His
ENST00000455624.6:c.5378G>A ENSP00000399524.2:p.Arg1793His