Canonical Allele Identifier: CA2665110380

Gene: SCN5A

Linked Data

• gnomAD v4: 3-38554422-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38554426dup , CM000665.2:g.38554426dup	GRCh38
NC_000003.11:g.38595917dup , CM000665.1:g.38595917dup	GRCh37
NC_000003.10:g.38570921dup	NCBI36
NG_008934.1:g.100250dup , LRG_289:g.100250dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000327956.7:c.4666dup	ENSP00000333674.7:p.Ile1556AsnfsTer?
ENST00000333535.9:c.4669dup	ENSP00000328968.4:p.Ile1557AsnfsTer?
ENST00000413689.6:c.4669dup MANE Plus Clinical	ENSP00000410257.1:p.Ile1557AsnfsTer?
ENST00000423572.7:c.4666dup MANE Select	ENSP00000398266.2:p.Ile1556AsnfsTer?
ENST00000333535.8:c.4669dup	ENSP00000328968.4:p.Ile1557AsnfsTer?
ENST00000413689.5:c.4669dup	ENSP00000410257.1:p.Ile1557AsnfsTer?
ENST00000414099.6:c.4615dup	ENSP00000398962.2:p.Ile1539AsnfsTer?
ENST00000423572.6:c.4666dup	ENSP00000398266.2:p.Ile1556AsnfsTer?
ENST00000425664.5:c.4615dup	ENSP00000416634.1:p.Ile1539AsnfsTer?
ENST00000449557.6:c.4507dup	ENSP00000413996.2:p.Ile1503AsnfsTer?
ENST00000450102.6:c.4507dup	ENSP00000403355.2:p.Ile1503AsnfsTer?
ENST00000451551.6:c.4507dup	ENSP00000388797.2:p.Ile1503AsnfsTer?
ENST00000455624.6:c.4666dup	ENSP00000399524.2:p.Ile1556AsnfsTer?
ENST00000464652.1:n.127dup
NM_000335.4:c.4666dup , LRG_289t2:c.4666dup	NP_000326.2:p.Ile1556AsnfsTer?
NM_001099404.1:c.4669dup , LRG_289t3:c.4669dup	NP_001092874.1:p.Ile1557AsnfsTer?
NM_001099405.1:c.4615dup	NP_001092875.1:p.Ile1539AsnfsTer?
NM_001160160.1:c.4666dup	NP_001153632.1:p.Ile1556AsnfsTer?
NM_001160161.1:c.4507dup	NP_001153633.1:p.Ile1503AsnfsTer?
NM_198056.2:c.4669dup , LRG_289t1:c.4669dup	NP_932173.1:p.Ile1557AsnfsTer?
XM_006713282.2:c.4669dup	XP_006713345.1:p.Ile1557AsnfsTer?
XM_011533991.1:c.4666dup	XP_011532293.1:p.Ile1556AsnfsTer?
XM_011533992.1:c.4540dup	XP_011532294.1:p.Ile1514AsnfsTer?
NM_001354701.1:c.4612dup	NP_001341630.1:p.Ile1538AsnfsTer?
XM_011533991.2:c.4666dup	XP_011532293.1:p.Ile1556AsnfsTer?
XM_017007017.1:c.4507dup	XP_016862506.1:p.Ile1503AsnfsTer?
NM_000335.5:c.4666dup MANE Select	NP_000326.2:p.Ile1556AsnfsTer?
NM_001160160.2:c.4666dup	NP_001153632.1:p.Ile1556AsnfsTer?
NM_001354701.2:c.4612dup	NP_001341630.1:p.Ile1538AsnfsTer?
NM_001099404.2:c.4669dup MANE Plus Clinical	NP_001092874.1:p.Ile1557AsnfsTer?
NM_001099405.2:c.4615dup	NP_001092875.1:p.Ile1539AsnfsTer?
NM_001160161.2:c.4507dup	NP_001153633.1:p.Ile1503AsnfsTer?
NM_198056.3:c.4669dup	NP_932173.1:p.Ile1557AsnfsTer?