Canonical Allele Identifier: CA1046987038

Gene: SCN5A

Linked Data

• gnomAD v3: 3-38551530-CTTCT-C
• gnomAD v4: 3-38551530-CTTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551531_38551534del , CM000665.2:g.38551531_38551534del	GRCh38
NC_000003.11:g.38593022_38593025del , CM000665.1:g.38593022_38593025del	GRCh37
NC_000003.10:g.38568026_38568029del	NCBI36
NG_008934.1:g.103139_103142del , LRG_289:g.103139_103142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4835_4838del	ENSP00000333674.7:p.Gln1612ArgfsTer17
ENST00000333535.9:c.4838_4841del	ENSP00000328968.4:p.Gln1613ArgfsTer17
ENST00000413689.6:c.4838_4841del MANE Plus Clinical	ENSP00000410257.1:p.Gln1613ArgfsTer17
ENST00000423572.7:c.4835_4838del MANE Select	ENSP00000398266.2:p.Gln1612ArgfsTer17
ENST00000333535.8:c.4838_4841del	ENSP00000328968.4:p.Gln1613ArgfsTer17
ENST00000413689.5:c.4838_4841del	ENSP00000410257.1:p.Gln1613ArgfsTer17
ENST00000414099.6:c.4784_4787del	ENSP00000398962.2:p.Gln1595ArgfsTer17
ENST00000423572.6:c.4835_4838del	ENSP00000398266.2:p.Gln1612ArgfsTer17
ENST00000425664.5:c.4784_4787del	ENSP00000416634.1:p.Gln1595ArgfsTer17
ENST00000449557.6:c.4676_4679del	ENSP00000413996.2:p.Gln1559ArgfsTer17
ENST00000450102.6:c.4676_4679del	ENSP00000403355.2:p.Gln1559ArgfsTer17
ENST00000451551.6:c.4676_4679del	ENSP00000388797.2:p.Gln1559ArgfsTer17
ENST00000455624.6:c.4739_4742del	ENSP00000399524.2:p.Gln1580ArgfsTer17
NM_000335.4:c.4835_4838del , LRG_289t2:c.4835_4838del	NP_000326.2:p.Gln1612ArgfsTer17
NM_001099404.1:c.4838_4841del , LRG_289t3:c.4838_4841del	NP_001092874.1:p.Gln1613ArgfsTer17
NM_001099405.1:c.4784_4787del	NP_001092875.1:p.Gln1595ArgfsTer17
NM_001160160.1:c.4739_4742del	NP_001153632.1:p.Gln1580ArgfsTer17
NM_001160161.1:c.4676_4679del	NP_001153633.1:p.Gln1559ArgfsTer17
NM_198056.2:c.4838_4841del , LRG_289t1:c.4838_4841del	NP_932173.1:p.Gln1613ArgfsTer17
XM_006713282.2:c.4838_4841del	XP_006713345.1:p.Gln1613ArgfsTer17
XM_011533991.1:c.4835_4838del	XP_011532293.1:p.Gln1612ArgfsTer17
XM_011533992.1:c.4709_4712del	XP_011532294.1:p.Gln1570ArgfsTer17
NM_001354701.1:c.4781_4784del	NP_001341630.1:p.Gln1594ArgfsTer17
XM_011533991.2:c.4835_4838del	XP_011532293.1:p.Gln1612ArgfsTer17
XM_017007017.1:c.4676_4679del	XP_016862506.1:p.Gln1559ArgfsTer17
NM_000335.5:c.4835_4838del MANE Select	NP_000326.2:p.Gln1612ArgfsTer17
NM_001160160.2:c.4739_4742del	NP_001153632.1:p.Gln1580ArgfsTer17
NM_001354701.2:c.4781_4784del	NP_001341630.1:p.Gln1594ArgfsTer17
NM_001099404.2:c.4838_4841del MANE Plus Clinical	NP_001092874.1:p.Gln1613ArgfsTer17
NM_001099405.2:c.4784_4787del	NP_001092875.1:p.Gln1595ArgfsTer17
NM_001160161.2:c.4676_4679del	NP_001153633.1:p.Gln1559ArgfsTer17
NM_198056.3:c.4838_4841del	NP_932173.1:p.Gln1613ArgfsTer17