Canonical Allele Identifier: CA352139966
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 999632
ClinVar RCV Id: RCV003656785
dbSNP Id: rs1224724151
gnomAD v2: 3-38592081-A-C
gnomAD v3: 3-38550590-A-C
gnomAD v4: 3-38550590-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38550590A>C , CM000665.2:g.38550590A>C GRCh38
NC_000003.11:g.38592081A>C , CM000665.1:g.38592081A>C GRCh37
NC_000003.10:g.38567085A>C NCBI36
NG_008934.1:g.104083T>G , LRG_289:g.104083T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327956.7:c.5779T>G ENSP00000333674.7:p.Phe1927Val
ENST00000333535.9:c.5782T>G ENSP00000328968.4:p.Phe1928Val
ENST00000413689.6:c.5782T>G MANE Plus Clinical ENSP00000410257.1:p.Phe1928Val
ENST00000423572.7:c.5779T>G MANE Select ENSP00000398266.2:p.Phe1927Val
ENST00000333535.8:c.5782T>G ENSP00000328968.4:p.Phe1928Val
ENST00000413689.5:c.5782T>G ENSP00000410257.1:p.Phe1928Val
ENST00000414099.6:c.5728T>G ENSP00000398962.2:p.Phe1910Val
ENST00000423572.6:c.5779T>G ENSP00000398266.2:p.Phe1927Val
ENST00000425664.5:c.5728T>G ENSP00000416634.1:p.Phe1910Val
ENST00000449557.6:c.5620T>G ENSP00000413996.2:p.Phe1874Val
ENST00000450102.6:c.5620T>G ENSP00000403355.2:p.Phe1874Val
ENST00000451551.6:c.5620T>G ENSP00000388797.2:p.Phe1874Val
ENST00000455624.6:c.5683T>G ENSP00000399524.2:p.Phe1895Val
NM_000335.4:c.5779T>G , LRG_289t2:c.5779T>G NP_000326.2:p.Phe1927Val
NM_001099404.1:c.5782T>G , LRG_289t3:c.5782T>G NP_001092874.1:p.Phe1928Val
NM_001099405.1:c.5728T>G NP_001092875.1:p.Phe1910Val
NM_001160160.1:c.5683T>G NP_001153632.1:p.Phe1895Val
NM_001160161.1:c.5620T>G NP_001153633.1:p.Phe1874Val
NM_198056.2:c.5782T>G , LRG_289t1:c.5782T>G NP_932173.1:p.Phe1928Val
XM_006713282.2:c.5782T>G XP_006713345.1:p.Phe1928Val
XM_011533991.1:c.5779T>G XP_011532293.1:p.Phe1927Val
XM_011533992.1:c.5653T>G XP_011532294.1:p.Phe1885Val
NM_001354701.1:c.5725T>G NP_001341630.1:p.Phe1909Val
XM_011533991.2:c.5779T>G XP_011532293.1:p.Phe1927Val
XM_017007017.1:c.5620T>G XP_016862506.1:p.Phe1874Val
NM_000335.5:c.5779T>G MANE Select NP_000326.2:p.Phe1927Val
NM_001160160.2:c.5683T>G NP_001153632.1:p.Phe1895Val
NM_001354701.2:c.5725T>G NP_001341630.1:p.Phe1909Val
NM_001099404.2:c.5782T>G MANE Plus Clinical NP_001092874.1:p.Phe1928Val
NM_001099405.2:c.5728T>G NP_001092875.1:p.Phe1910Val
NM_001160161.2:c.5620T>G NP_001153633.1:p.Phe1874Val
NM_198056.3:c.5782T>G NP_932173.1:p.Phe1928Val