Canonical Allele Identifier: CA2577553273

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38554421_38554425dup , CM000665.2:g.38554421_38554425dup	GRCh38
NC_000003.11:g.38595912_38595916dup , CM000665.1:g.38595912_38595916dup	GRCh37
NC_000003.10:g.38570916_38570920dup	NCBI36
NG_008934.1:g.100250_100254dup , LRG_289:g.100250_100254dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000327956.7:c.4666_4670dup	ENSP00000333674.7:p.Asn1557LysfsTer?
ENST00000333535.9:c.4669_4673dup	ENSP00000328968.4:p.Asn1558LysfsTer?
ENST00000413689.6:c.4669_4673dup MANE Plus Clinical	ENSP00000410257.1:p.Asn1558LysfsTer?
ENST00000423572.7:c.4666_4670dup MANE Select	ENSP00000398266.2:p.Asn1557LysfsTer?
ENST00000333535.8:c.4669_4673dup	ENSP00000328968.4:p.Asn1558LysfsTer?
ENST00000413689.5:c.4669_4673dup	ENSP00000410257.1:p.Asn1558LysfsTer?
ENST00000414099.6:c.4615_4619dup	ENSP00000398962.2:p.Asn1540LysfsTer?
ENST00000423572.6:c.4666_4670dup	ENSP00000398266.2:p.Asn1557LysfsTer?
ENST00000425664.5:c.4615_4619dup	ENSP00000416634.1:p.Asn1540LysfsTer?
ENST00000449557.6:c.4507_4511dup	ENSP00000413996.2:p.Asn1504LysfsTer?
ENST00000450102.6:c.4507_4511dup	ENSP00000403355.2:p.Asn1504LysfsTer?
ENST00000451551.6:c.4507_4511dup	ENSP00000388797.2:p.Asn1504LysfsTer?
ENST00000455624.6:c.4666_4670dup	ENSP00000399524.2:p.Asn1557LysfsTer?
ENST00000464652.1:n.127_131dup
NM_000335.4:c.4666_4670dup , LRG_289t2:c.4666_4670dup	NP_000326.2:p.Asn1557LysfsTer?
NM_001099404.1:c.4669_4673dup , LRG_289t3:c.4669_4673dup	NP_001092874.1:p.Asn1558LysfsTer?
NM_001099405.1:c.4615_4619dup	NP_001092875.1:p.Asn1540LysfsTer?
NM_001160160.1:c.4666_4670dup	NP_001153632.1:p.Asn1557LysfsTer?
NM_001160161.1:c.4507_4511dup	NP_001153633.1:p.Asn1504LysfsTer?
NM_198056.2:c.4669_4673dup , LRG_289t1:c.4669_4673dup	NP_932173.1:p.Asn1558LysfsTer?
XM_006713282.2:c.4669_4673dup	XP_006713345.1:p.Asn1558LysfsTer?
XM_011533991.1:c.4666_4670dup	XP_011532293.1:p.Asn1557LysfsTer?
XM_011533992.1:c.4540_4544dup	XP_011532294.1:p.Asn1515LysfsTer?
NM_001354701.1:c.4612_4616dup	NP_001341630.1:p.Asn1539LysfsTer?
XM_011533991.2:c.4666_4670dup	XP_011532293.1:p.Asn1557LysfsTer?
XM_017007017.1:c.4507_4511dup	XP_016862506.1:p.Asn1504LysfsTer?
NM_000335.5:c.4666_4670dup MANE Select	NP_000326.2:p.Asn1557LysfsTer?
NM_001160160.2:c.4666_4670dup	NP_001153632.1:p.Asn1557LysfsTer?
NM_001354701.2:c.4612_4616dup	NP_001341630.1:p.Asn1539LysfsTer?
NM_001099404.2:c.4669_4673dup MANE Plus Clinical	NP_001092874.1:p.Asn1558LysfsTer?
NM_001099405.2:c.4615_4619dup	NP_001092875.1:p.Asn1540LysfsTer?
NM_001160161.2:c.4507_4511dup	NP_001153633.1:p.Asn1504LysfsTer?
NM_198056.3:c.4669_4673dup	NP_932173.1:p.Asn1558LysfsTer?