Canonical Allele Identifier: CA1358560907
Gene: SCN5A HGNC NCBI

Linked Data

dbSNP Id: rs2060973939

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38548633_38548636dup , CM000665.2:g.38548633_38548636dup GRCh38
NC_000003.11:g.38590124_38590127dup , CM000665.1:g.38590124_38590127dup GRCh37
NC_000003.10:g.38565128_38565131dup NCBI36
NG_008934.1:g.106037_106040dup , LRG_289:g.106037_106040dup

Transcript Alleles

HGVS Amino-acid change
ENST00000327956.7:c.*1685_*1688dup ENSP00000333674.7:n.*1685_*1688dup
ENST00000333535.9:c.*1685_*1688dup ENSP00000328968.4:n.*1685_*1688dup
ENST00000413689.6:c.*1685_*1688dup MANE Plus Clinical ENSP00000410257.1:n.*1685_*1688dup
ENST00000423572.7:c.*1685_*1688dup MANE Select ENSP00000398266.2:n.*1685_*1688dup
ENST00000333535.8:c.*1685_*1688dup ENSP00000328968.4:n.*1685_*1688dup
ENST00000413689.5:c.*1685_*1688dup ENSP00000410257.1:n.*1685_*1688dup
ENST00000414099.6:c.*1685_*1688dup ENSP00000398962.2:n.*1685_*1688dup
ENST00000423572.6:c.*1685_*1688dup ENSP00000398266.2:n.*1685_*1688dup
ENST00000425664.5:c.*1685_*1688dup ENSP00000416634.1:n.*1685_*1688dup
ENST00000451551.6:c.*1685_*1688dup ENSP00000388797.2:n.*1685_*1688dup
NM_000335.4:c.*1685_*1688dup , LRG_289t2:c.*1685_*1688dup NP_000326.2:n.*1685_*1688dup
NM_001099404.1:c.*1685_*1688dup , LRG_289t3:c.*1685_*1688dup NP_001092874.1:n.*1685_*1688dup
NM_001099405.1:c.*1685_*1688dup NP_001092875.1:n.*1685_*1688dup
NM_001160160.1:c.*1685_*1688dup NP_001153632.1:n.*1685_*1688dup
NM_001160161.1:c.*1685_*1688dup NP_001153633.1:n.*1685_*1688dup
NM_198056.2:c.*1685_*1688dup , LRG_289t1:c.*1685_*1688dup NP_932173.1:n.*1685_*1688dup
XM_006713282.2:c.*1685_*1688dup XP_006713345.1:n.*1685_*1688dup
XM_011533991.1:c.*1685_*1688dup XP_011532293.1:n.*1685_*1688dup
XM_011533992.1:c.*1685_*1688dup XP_011532294.1:n.*1685_*1688dup
NM_001354701.1:c.*1685_*1688dup NP_001341630.1:n.*1685_*1688dup
XM_011533991.2:c.*1685_*1688dup XP_011532293.1:n.*1685_*1688dup
XM_017007017.1:c.*1685_*1688dup XP_016862506.1:n.*1685_*1688dup
NM_000335.5:c.*1685_*1688dup MANE Select NP_000326.2:n.*1685_*1688dup
NM_001160160.2:c.*1685_*1688dup NP_001153632.1:n.*1685_*1688dup
NM_001354701.2:c.*1685_*1688dup NP_001341630.1:n.*1685_*1688dup
NM_001099404.2:c.*1685_*1688dup MANE Plus Clinical NP_001092874.1:n.*1685_*1688dup
NM_001099405.2:c.*1685_*1688dup NP_001092875.1:n.*1685_*1688dup
NM_001160161.2:c.*1685_*1688dup NP_001153633.1:n.*1685_*1688dup
NM_198056.3:c.*1685_*1688dup NP_932173.1:n.*1685_*1688dup