Canonical Allele Identifier: CA2577565985

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38633395del , CM000665.2:g.38633395del	GRCh38
NC_000003.11:g.38674886del , CM000665.1:g.38674886del	GRCh37
NC_000003.10:g.38649890del	NCBI36
NG_008934.1:g.21280del , LRG_289:g.21280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.-52-34del	ENSP00000333674.7:n.-52-34del
ENST00000333535.9:c.-52-34del	ENSP00000328968.4:n.-52-34del
ENST00000413689.6:c.-52-34del MANE Plus Clinical	ENSP00000410257.1:n.-52-34del
ENST00000423572.7:c.-52-34del MANE Select	ENSP00000398266.2:n.-52-34del
ENST00000327956.6:c.-52-34del	ENSP00000333674.6:n.-52-34del
ENST00000333535.8:c.-52-34del	ENSP00000328968.4:n.-52-34del
ENST00000413689.5:c.-52-34del	ENSP00000410257.1:n.-52-34del
ENST00000425664.5:c.-52-34del	ENSP00000416634.1:n.-52-34del
ENST00000451551.6:c.-52-34del	ENSP00000388797.2:n.-52-34del
ENST00000491944.1:n.144-34del
NM_000335.4:c.-52-34del , LRG_289t2:c.-52-34del	NP_000326.2:n.-52-34del
NM_001099404.1:c.-52-34del , LRG_289t3:c.-52-34del	NP_001092874.1:n.-52-34del
NM_001099405.1:c.-52-34del	NP_001092875.1:n.-52-34del
NM_001160160.1:c.-52-34del	NP_001153632.1:n.-52-34del
NM_001160161.1:c.-52-34del	NP_001153633.1:n.-52-34del
NM_198056.2:c.-52-34del , LRG_289t1:c.-52-34del	NP_932173.1:n.-52-34del
XM_006713282.2:c.-52-34del	XP_006713345.1:n.-52-34del
XM_011533991.1:c.-52-34del	XP_011532293.1:n.-52-34del
XM_011533992.1:c.-52-34del	XP_011532294.1:n.-52-34del
NM_001354701.1:c.-52-34del	NP_001341630.1:n.-52-34del
XM_011533991.2:c.-52-34del	XP_011532293.1:n.-52-34del
XM_017007017.1:c.-52-34del	XP_016862506.1:n.-52-34del
NM_000335.5:c.-52-34del MANE Select	NP_000326.2:n.-52-34del
NM_001160160.2:c.-52-34del	NP_001153632.1:n.-52-34del
NM_001354701.2:c.-52-34del	NP_001341630.1:n.-52-34del
NM_001099404.2:c.-52-34del MANE Plus Clinical	NP_001092874.1:n.-52-34del
NM_001099405.2:c.-52-34del	NP_001092875.1:n.-52-34del
NM_001160161.2:c.-52-34del	NP_001153633.1:n.-52-34del
NM_198056.3:c.-52-34del	NP_932173.1:n.-52-34del