Canonical Allele Identifier: CA2665111236
Gene: SCN5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38557207_38557208insCCAAGCAGCCAGGAGCCTCAGGTGCCTGACTTGGTGG , CM000665.2:g.38557207_38557208insCCAAGCAGCCAGGAGCCTCAGGTGCCTGACTTGGTGG GRCh38
NC_000003.11:g.38598698_38598699insCCAAGCAGCCAGGAGCCTCAGGTGCCTGACTTGGTGG , CM000665.1:g.38598698_38598699insCCAAGCAGCCAGGAGCCTCAGGTGCCTGACTTGGTGG GRCh37
NC_000003.10:g.38573702_38573703insCCAAGCAGCCAGGAGCCTCAGGTGCCTGACTTGGTGG NCBI36
NG_008934.1:g.97494_97495insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG , LRG_289:g.97494_97495insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000327956.7:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000333674.7:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000333535.9:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000328968.4:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000413689.6:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG MANE Plus Clinical ENSP00000410257.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000423572.7:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG MANE Select ENSP00000398266.2:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000333535.8:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000328968.4:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000413689.5:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000410257.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000414099.6:c.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000398962.2:n.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGG...
ENST00000423572.6:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000398266.2:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000425664.5:c.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000416634.1:n.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGG...
ENST00000449557.6:c.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000413996.2:n.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000450102.6:c.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000403355.2:n.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000451551.6:c.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000388797.2:n.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCA...
ENST00000455624.6:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG ENSP00000399524.2:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCA...
NM_000335.4:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG , LRG_289t2:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_000326.2:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAG...
NM_001099404.1:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG , LRG_289t3:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001092874.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_001099405.1:c.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001092875.1:n.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGGCAC...
NM_001160160.1:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001153632.1:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_001160161.1:c.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001153633.1:n.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_198056.2:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG , LRG_289t1:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_932173.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAG...
XM_006713282.2:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG XP_006713345.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCT...
XM_011533991.1:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG XP_011532293.1:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCT...
XM_011533992.1:c.4170+52_4170+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG XP_011532294.1:n.4170+52_4170+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_001354701.1:c.4243-601_4243-600insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001341630.1:n.4243-601_4243-600insCTGCTTGGCCACCAAGTCAGGCAC...
XM_011533991.2:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG XP_011532293.1:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCT...
XM_017007017.1:c.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG XP_016862506.1:n.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_000335.5:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG MANE Select NP_000326.2:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAG...
NM_001160160.2:c.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001153632.1:n.4296+52_4296+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_001354701.2:c.4243-601_4243-600insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001341630.1:n.4243-601_4243-600insCTGCTTGGCCACCAAGTCAGGCAC...
NM_001099404.2:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG MANE Plus Clinical NP_001092874.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_001099405.2:c.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001092875.1:n.4246-601_4246-600insCTGCTTGGCCACCAAGTCAGGCAC...
NM_001160161.2:c.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_001153633.1:n.4137+52_4137+53insCTGCTTGGCCACCAAGTCAGGCACCT...
NM_198056.3:c.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAGGCTCCTGG NP_932173.1:n.4299+52_4299+53insCTGCTTGGCCACCAAGTCAGGCACCTGAG...