Canonical Allele Identifier: CA019134
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67985
dbSNP Id: rs199473634
gnomAD v2: 3-38592527-G-A
gnomAD v3: 3-38551036-G-A
gnomAD v4: 3-38551036-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38551036G>A , CM000665.2:g.38551036G>A GRCh38
NC_000003.11:g.38592527G>A , CM000665.1:g.38592527G>A GRCh37
NC_000003.10:g.38567531G>A NCBI36
NG_008934.1:g.103637C>T , LRG_289:g.103637C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327956.7:c.5333C>T ENSP00000333674.7:p.Thr1778Met
ENST00000333535.9:c.5336C>T ENSP00000328968.4:p.Thr1779Met
ENST00000413689.6:c.5336C>T MANE Plus Clinical ENSP00000410257.1:p.Thr1779Met
ENST00000423572.7:c.5333C>T MANE Select ENSP00000398266.2:p.Thr1778Met
ENST00000333535.8:c.5336C>T ENSP00000328968.4:p.Thr1779Met
ENST00000413689.5:c.5336C>T ENSP00000410257.1:p.Thr1779Met
ENST00000414099.6:c.5282C>T ENSP00000398962.2:p.Thr1761Met
ENST00000423572.6:c.5333C>T ENSP00000398266.2:p.Thr1778Met
ENST00000425664.5:c.5282C>T ENSP00000416634.1:p.Thr1761Met
ENST00000449557.6:c.5174C>T ENSP00000413996.2:p.Thr1725Met
ENST00000450102.6:c.5174C>T ENSP00000403355.2:p.Thr1725Met
ENST00000451551.6:c.5174C>T ENSP00000388797.2:p.Thr1725Met
ENST00000455624.6:c.5237C>T ENSP00000399524.2:p.Thr1746Met
NM_000335.4:c.5333C>T , LRG_289t2:c.5333C>T NP_000326.2:p.Thr1778Met
NM_001099404.1:c.5336C>T , LRG_289t3:c.5336C>T NP_001092874.1:p.Thr1779Met
NM_001099405.1:c.5282C>T NP_001092875.1:p.Thr1761Met
NM_001160160.1:c.5237C>T NP_001153632.1:p.Thr1746Met
NM_001160161.1:c.5174C>T NP_001153633.1:p.Thr1725Met
NM_198056.2:c.5336C>T , LRG_289t1:c.5336C>T NP_932173.1:p.Thr1779Met
XM_006713282.2:c.5336C>T XP_006713345.1:p.Thr1779Met
XM_011533991.1:c.5333C>T XP_011532293.1:p.Thr1778Met
XM_011533992.1:c.5207C>T XP_011532294.1:p.Thr1736Met
NM_001354701.1:c.5279C>T NP_001341630.1:p.Thr1760Met
XM_011533991.2:c.5333C>T XP_011532293.1:p.Thr1778Met
XM_017007017.1:c.5174C>T XP_016862506.1:p.Thr1725Met
NM_000335.5:c.5333C>T MANE Select NP_000326.2:p.Thr1778Met
NM_001160160.2:c.5237C>T NP_001153632.1:p.Thr1746Met
NM_001354701.2:c.5279C>T NP_001341630.1:p.Thr1760Met
NM_001099404.2:c.5336C>T MANE Plus Clinical NP_001092874.1:p.Thr1779Met
NM_001099405.2:c.5282C>T NP_001092875.1:p.Thr1761Met
NM_001160161.2:c.5174C>T NP_001153633.1:p.Thr1725Met
NM_198056.3:c.5336C>T NP_932173.1:p.Thr1779Met