Canonical Allele Identifier: CA1046987146

Gene: SCN5A

Linked Data

• gnomAD v3: 3-38551540-A-AG
• gnomAD v4: 3-38551540-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551540_38551541insG , CM000665.2:g.38551540_38551541insG	GRCh38
NC_000003.11:g.38593031_38593032insG , CM000665.1:g.38593031_38593032insG	GRCh37
NC_000003.10:g.38568035_38568036insG	NCBI36
NG_008934.1:g.103132_103133insC , LRG_289:g.103132_103133insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4828_4829insC	ENSP00000333674.7:p.Ile1610ThrfsTer?
ENST00000333535.9:c.4831_4832insC	ENSP00000328968.4:p.Ile1611ThrfsTer?
ENST00000413689.6:c.4831_4832insC MANE Plus Clinical	ENSP00000410257.1:p.Ile1611ThrfsTer?
ENST00000423572.7:c.4828_4829insC MANE Select	ENSP00000398266.2:p.Ile1610ThrfsTer?
ENST00000333535.8:c.4831_4832insC	ENSP00000328968.4:p.Ile1611ThrfsTer?
ENST00000413689.5:c.4831_4832insC	ENSP00000410257.1:p.Ile1611ThrfsTer?
ENST00000414099.6:c.4777_4778insC	ENSP00000398962.2:p.Ile1593ThrfsTer?
ENST00000423572.6:c.4828_4829insC	ENSP00000398266.2:p.Ile1610ThrfsTer?
ENST00000425664.5:c.4777_4778insC	ENSP00000416634.1:p.Ile1593ThrfsTer?
ENST00000449557.6:c.4669_4670insC	ENSP00000413996.2:p.Ile1557ThrfsTer?
ENST00000450102.6:c.4669_4670insC	ENSP00000403355.2:p.Ile1557ThrfsTer?
ENST00000451551.6:c.4669_4670insC	ENSP00000388797.2:p.Ile1557ThrfsTer?
ENST00000455624.6:c.4732_4733insC	ENSP00000399524.2:p.Ile1578ThrfsTer?
NM_000335.4:c.4828_4829insC , LRG_289t2:c.4828_4829insC	NP_000326.2:p.Ile1610ThrfsTer?
NM_001099404.1:c.4831_4832insC , LRG_289t3:c.4831_4832insC	NP_001092874.1:p.Ile1611ThrfsTer?
NM_001099405.1:c.4777_4778insC	NP_001092875.1:p.Ile1593ThrfsTer?
NM_001160160.1:c.4732_4733insC	NP_001153632.1:p.Ile1578ThrfsTer?
NM_001160161.1:c.4669_4670insC	NP_001153633.1:p.Ile1557ThrfsTer?
NM_198056.2:c.4831_4832insC , LRG_289t1:c.4831_4832insC	NP_932173.1:p.Ile1611ThrfsTer?
XM_006713282.2:c.4831_4832insC	XP_006713345.1:p.Ile1611ThrfsTer?
XM_011533991.1:c.4828_4829insC	XP_011532293.1:p.Ile1610ThrfsTer?
XM_011533992.1:c.4702_4703insC	XP_011532294.1:p.Ile1568ThrfsTer?
NM_001354701.1:c.4774_4775insC	NP_001341630.1:p.Ile1592ThrfsTer?
XM_011533991.2:c.4828_4829insC	XP_011532293.1:p.Ile1610ThrfsTer?
XM_017007017.1:c.4669_4670insC	XP_016862506.1:p.Ile1557ThrfsTer?
NM_000335.5:c.4828_4829insC MANE Select	NP_000326.2:p.Ile1610ThrfsTer?
NM_001160160.2:c.4732_4733insC	NP_001153632.1:p.Ile1578ThrfsTer?
NM_001354701.2:c.4774_4775insC	NP_001341630.1:p.Ile1592ThrfsTer?
NM_001099404.2:c.4831_4832insC MANE Plus Clinical	NP_001092874.1:p.Ile1611ThrfsTer?
NM_001099405.2:c.4777_4778insC	NP_001092875.1:p.Ile1593ThrfsTer?
NM_001160161.2:c.4669_4670insC	NP_001153633.1:p.Ile1557ThrfsTer?
NM_198056.3:c.4831_4832insC	NP_932173.1:p.Ile1611ThrfsTer?