Canonical Allele Identifier: CA1046987041

Gene: SCN5A

Linked Data

• dbSNP Id: rs2061040793
• gnomAD v3: 3-38551530-CTTCTGG-C
• gnomAD v4: 3-38551530-CTTCTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551531_38551536del , CM000665.2:g.38551531_38551536del	GRCh38
NC_000003.11:g.38593022_38593027del , CM000665.1:g.38593022_38593027del	GRCh37
NC_000003.10:g.38568026_38568031del	NCBI36
NG_008934.1:g.103137_103142del , LRG_289:g.103137_103142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4833_4838del	ENSP00000333674.7:p.Ile1611_Lys1613delinsMet
ENST00000333535.9:c.4836_4841del	ENSP00000328968.4:p.Ile1612_Lys1614delinsMet
ENST00000413689.6:c.4836_4841del MANE Plus Clinical	ENSP00000410257.1:p.Ile1612_Lys1614delinsMet
ENST00000423572.7:c.4833_4838del MANE Select	ENSP00000398266.2:p.Ile1611_Lys1613delinsMet
ENST00000333535.8:c.4836_4841del	ENSP00000328968.4:p.Ile1612_Lys1614delinsMet
ENST00000413689.5:c.4836_4841del	ENSP00000410257.1:p.Ile1612_Lys1614delinsMet
ENST00000414099.6:c.4782_4787del	ENSP00000398962.2:p.Ile1594_Lys1596delinsMet
ENST00000423572.6:c.4833_4838del	ENSP00000398266.2:p.Ile1611_Lys1613delinsMet
ENST00000425664.5:c.4782_4787del	ENSP00000416634.1:p.Ile1594_Lys1596delinsMet
ENST00000449557.6:c.4674_4679del	ENSP00000413996.2:p.Ile1558_Lys1560delinsMet
ENST00000450102.6:c.4674_4679del	ENSP00000403355.2:p.Ile1558_Lys1560delinsMet
ENST00000451551.6:c.4674_4679del	ENSP00000388797.2:p.Ile1558_Lys1560delinsMet
ENST00000455624.6:c.4737_4742del	ENSP00000399524.2:p.Ile1579_Lys1581delinsMet
NM_000335.4:c.4833_4838del , LRG_289t2:c.4833_4838del	NP_000326.2:p.Ile1611_Lys1613delinsMet
NM_001099404.1:c.4836_4841del , LRG_289t3:c.4836_4841del	NP_001092874.1:p.Ile1612_Lys1614delinsMet
NM_001099405.1:c.4782_4787del	NP_001092875.1:p.Ile1594_Lys1596delinsMet
NM_001160160.1:c.4737_4742del	NP_001153632.1:p.Ile1579_Lys1581delinsMet
NM_001160161.1:c.4674_4679del	NP_001153633.1:p.Ile1558_Lys1560delinsMet
NM_198056.2:c.4836_4841del , LRG_289t1:c.4836_4841del	NP_932173.1:p.Ile1612_Lys1614delinsMet
XM_006713282.2:c.4836_4841del	XP_006713345.1:p.Ile1612_Lys1614delinsMet
XM_011533991.1:c.4833_4838del	XP_011532293.1:p.Ile1611_Lys1613delinsMet
XM_011533992.1:c.4707_4712del	XP_011532294.1:p.Ile1569_Lys1571delinsMet
NM_001354701.1:c.4779_4784del	NP_001341630.1:p.Ile1593_Lys1595delinsMet
XM_011533991.2:c.4833_4838del	XP_011532293.1:p.Ile1611_Lys1613delinsMet
XM_017007017.1:c.4674_4679del	XP_016862506.1:p.Ile1558_Lys1560delinsMet
NM_000335.5:c.4833_4838del MANE Select	NP_000326.2:p.Ile1611_Lys1613delinsMet
NM_001160160.2:c.4737_4742del	NP_001153632.1:p.Ile1579_Lys1581delinsMet
NM_001354701.2:c.4779_4784del	NP_001341630.1:p.Ile1593_Lys1595delinsMet
NM_001099404.2:c.4836_4841del MANE Plus Clinical	NP_001092874.1:p.Ile1612_Lys1614delinsMet
NM_001099405.2:c.4782_4787del	NP_001092875.1:p.Ile1594_Lys1596delinsMet
NM_001160161.2:c.4674_4679del	NP_001153633.1:p.Ile1558_Lys1560delinsMet
NM_198056.3:c.4836_4841del	NP_932173.1:p.Ile1612_Lys1614delinsMet