Canonical Allele Identifier: CA906903359

Gene: SCN5A

Linked Data

• dbSNP Id: rs1350078004
• gnomAD v3: 3-38566207-TCTC-T
• gnomAD v4: 3-38566207-TCTC-T
• MyVariant Identifiers: chr3:g.38607699_38607701del (hg19) ; chr3:g.38566208_38566210del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38566208_38566210del , CM000665.2:g.38566208_38566210del	GRCh38
NC_000003.11:g.38607699_38607701del , CM000665.1:g.38607699_38607701del	GRCh37
NC_000003.10:g.38582703_38582705del	NCBI36
NG_008934.1:g.88463_88465del , LRG_289:g.88463_88465del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.3837+199_3837+201del	ENSP00000333674.7:n.3837+199_3837+201del
ENST00000333535.9:c.3840+199_3840+201del	ENSP00000328968.4:n.3840+199_3840+201del
ENST00000413689.6:c.3840+199_3840+201del MANE Plus Clinical	ENSP00000410257.1:n.3840+199_3840+201del
ENST00000423572.7:c.3837+199_3837+201del MANE Select	ENSP00000398266.2:n.3837+199_3837+201del
ENST00000333535.8:c.3840+199_3840+201del	ENSP00000328968.4:n.3840+199_3840+201del
ENST00000413689.5:c.3840+199_3840+201del	ENSP00000410257.1:n.3840+199_3840+201del
ENST00000414099.6:c.3840+199_3840+201del	ENSP00000398962.2:n.3840+199_3840+201del
ENST00000423572.6:c.3837+199_3837+201del	ENSP00000398266.2:n.3837+199_3837+201del
ENST00000425664.5:c.3840+199_3840+201del	ENSP00000416634.1:n.3840+199_3840+201del
ENST00000449557.6:c.3678+199_3678+201del	ENSP00000413996.2:n.3678+199_3678+201del
ENST00000450102.6:c.3678+199_3678+201del	ENSP00000403355.2:n.3678+199_3678+201del
ENST00000451551.6:c.3678+199_3678+201del	ENSP00000388797.2:n.3678+199_3678+201del
ENST00000455624.6:c.3837+199_3837+201del	ENSP00000399524.2:n.3837+199_3837+201del
NM_000335.4:c.3837+199_3837+201del , LRG_289t2:c.3837+199_3837+201del	NP_000326.2:n.3837+199_3837+201del
NM_001099404.1:c.3840+199_3840+201del , LRG_289t3:c.3840+199_3840+201del	NP_001092874.1:n.3840+199_3840+201del
NM_001099405.1:c.3840+199_3840+201del	NP_001092875.1:n.3840+199_3840+201del
NM_001160160.1:c.3837+199_3837+201del	NP_001153632.1:n.3837+199_3837+201del
NM_001160161.1:c.3678+199_3678+201del	NP_001153633.1:n.3678+199_3678+201del
NM_198056.2:c.3840+199_3840+201del , LRG_289t1:c.3840+199_3840+201del	NP_932173.1:n.3840+199_3840+201del
XM_006713282.2:c.3840+199_3840+201del	XP_006713345.1:n.3840+199_3840+201del
XM_011533991.1:c.3837+199_3837+201del	XP_011532293.1:n.3837+199_3837+201del
XM_011533992.1:c.3711+199_3711+201del	XP_011532294.1:n.3711+199_3711+201del
NM_001354701.1:c.3837+199_3837+201del	NP_001341630.1:n.3837+199_3837+201del
XM_011533991.2:c.3837+199_3837+201del	XP_011532293.1:n.3837+199_3837+201del
XM_017007017.1:c.3678+199_3678+201del	XP_016862506.1:n.3678+199_3678+201del
NM_000335.5:c.3837+199_3837+201del MANE Select	NP_000326.2:n.3837+199_3837+201del
NM_001160160.2:c.3837+199_3837+201del	NP_001153632.1:n.3837+199_3837+201del
NM_001354701.2:c.3837+199_3837+201del	NP_001341630.1:n.3837+199_3837+201del
NM_001099404.2:c.3840+199_3840+201del MANE Plus Clinical	NP_001092874.1:n.3840+199_3840+201del
NM_001099405.2:c.3840+199_3840+201del	NP_001092875.1:n.3840+199_3840+201del
NM_001160161.2:c.3678+199_3678+201del	NP_001153633.1:n.3678+199_3678+201del
NM_198056.3:c.3840+199_3840+201del	NP_932173.1:n.3840+199_3840+201del