Canonical Allele Identifier: CA2586965758

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38560147del , CM000665.2:g.38560147del	GRCh38
NC_000003.11:g.38601638del , CM000665.1:g.38601638del	GRCh37
NC_000003.10:g.38576642del	NCBI36
NG_008934.1:g.94527del , LRG_289:g.94527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4242+1del
ENST00000333535.9:c.4245+1del
ENST00000413689.6:c.4245+1del
ENST00000423572.7:c.4242+1del
ENST00000333535.8:c.4245+1del
ENST00000413689.5:c.4245+1del
ENST00000414099.6:c.4245+1del
ENST00000423572.6:c.4242+1del
ENST00000425664.5:c.4245+1del
ENST00000449557.6:c.4083+1del
ENST00000450102.6:c.4083+1del
ENST00000451551.6:c.4083+1del
ENST00000455624.6:c.4242+1del
NM_000335.4:c.4242+1del , LRG_289t2:c.4242+1del
NM_001099404.1:c.4245+1del , LRG_289t3:c.4245+1del
NM_001099405.1:c.4245+1del
NM_001160160.1:c.4242+1del
NM_001160161.1:c.4083+1del
NM_198056.2:c.4245+1del , LRG_289t1:c.4245+1del
XM_006713282.2:c.4245+1del
XM_011533991.1:c.4242+1del
XM_011533992.1:c.4116+1del
NM_001354701.1:c.4242+1del
XM_011533991.2:c.4242+1del
XM_017007017.1:c.4083+1del
NM_000335.5:c.4242+1del
NM_001160160.2:c.4242+1del
NM_001354701.2:c.4242+1del
NM_001099404.2:c.4245+1del
NM_001099405.2:c.4245+1del
NM_001160161.2:c.4083+1del
NM_198056.3:c.4245+1del