Canonical Allele Identifier: CA2586965736

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38550696del , CM000665.2:g.38550696del	GRCh38
NC_000003.11:g.38592187del , CM000665.1:g.38592187del	GRCh37
NC_000003.10:g.38567191del	NCBI36
NG_008934.1:g.103977del , LRG_289:g.103977del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.5673del	ENSP00000333674.7:p.Thr1892ProfsTer29
ENST00000333535.9:c.5676del	ENSP00000328968.4:p.Thr1893ProfsTer29
ENST00000413689.6:c.5676del MANE Plus Clinical	ENSP00000410257.1:p.Thr1893ProfsTer29
ENST00000423572.7:c.5673del MANE Select	ENSP00000398266.2:p.Thr1892ProfsTer29
ENST00000333535.8:c.5676del	ENSP00000328968.4:p.Thr1893ProfsTer29
ENST00000413689.5:c.5676del	ENSP00000410257.1:p.Thr1893ProfsTer29
ENST00000414099.6:c.5622del	ENSP00000398962.2:p.Thr1875ProfsTer29
ENST00000423572.6:c.5673del	ENSP00000398266.2:p.Thr1892ProfsTer29
ENST00000425664.5:c.5622del	ENSP00000416634.1:p.Thr1875ProfsTer29
ENST00000449557.6:c.5514del	ENSP00000413996.2:p.Thr1839ProfsTer29
ENST00000450102.6:c.5514del	ENSP00000403355.2:p.Thr1839ProfsTer29
ENST00000451551.6:c.5514del	ENSP00000388797.2:p.Thr1839ProfsTer29
ENST00000455624.6:c.5577del	ENSP00000399524.2:p.Thr1860ProfsTer29
NM_000335.4:c.5673del , LRG_289t2:c.5673del	NP_000326.2:p.Thr1892ProfsTer29
NM_001099404.1:c.5676del , LRG_289t3:c.5676del	NP_001092874.1:p.Thr1893ProfsTer29
NM_001099405.1:c.5622del	NP_001092875.1:p.Thr1875ProfsTer29
NM_001160160.1:c.5577del	NP_001153632.1:p.Thr1860ProfsTer29
NM_001160161.1:c.5514del	NP_001153633.1:p.Thr1839ProfsTer29
NM_198056.2:c.5676del , LRG_289t1:c.5676del	NP_932173.1:p.Thr1893ProfsTer29
XM_006713282.2:c.5676del	XP_006713345.1:p.Thr1893ProfsTer29
XM_011533991.1:c.5673del	XP_011532293.1:p.Thr1892ProfsTer29
XM_011533992.1:c.5547del	XP_011532294.1:p.Thr1850ProfsTer29
NM_001354701.1:c.5619del	NP_001341630.1:p.Thr1874ProfsTer29
XM_011533991.2:c.5673del	XP_011532293.1:p.Thr1892ProfsTer29
XM_017007017.1:c.5514del	XP_016862506.1:p.Thr1839ProfsTer29
NM_000335.5:c.5673del MANE Select	NP_000326.2:p.Thr1892ProfsTer29
NM_001160160.2:c.5577del	NP_001153632.1:p.Thr1860ProfsTer29
NM_001354701.2:c.5619del	NP_001341630.1:p.Thr1874ProfsTer29
NM_001099404.2:c.5676del MANE Plus Clinical	NP_001092874.1:p.Thr1893ProfsTer29
NM_001099405.2:c.5622del	NP_001092875.1:p.Thr1875ProfsTer29
NM_001160161.2:c.5514del	NP_001153633.1:p.Thr1839ProfsTer29
NM_198056.3:c.5676del	NP_932173.1:p.Thr1893ProfsTer29