Canonical Allele Identifier: CA1358557264

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551050_38551051delinsGT , CM000665.2:g.38551050_38551051delinsGT	GRCh38
NC_000003.11:g.38592541_38592542delinsGT , CM000665.1:g.38592541_38592542delinsGT	GRCh37
NC_000003.10:g.38567545_38567546delinsGT	NCBI36
NG_008934.1:g.103622_103623delinsAC , LRG_289:g.103622_103623delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.5318_5319delinsAC	ENSP00000333674.7:p.Asn1773=
ENST00000333535.9:c.5321_5322delinsAC	ENSP00000328968.4:p.Asn1774=
ENST00000413689.6:c.5321_5322delinsAC MANE Plus Clinical	ENSP00000410257.1:p.Asn1774=
ENST00000423572.7:c.5318_5319delinsAC MANE Select	ENSP00000398266.2:p.Asn1773=
ENST00000333535.8:c.5321_5322delinsAC	ENSP00000328968.4:p.Asn1774=
ENST00000413689.5:c.5321_5322delinsAC	ENSP00000410257.1:p.Asn1774=
ENST00000414099.6:c.5267_5268delinsAC	ENSP00000398962.2:p.Asn1756=
ENST00000423572.6:c.5318_5319delinsAC	ENSP00000398266.2:p.Asn1773=
ENST00000425664.5:c.5267_5268delinsAC	ENSP00000416634.1:p.Asn1756=
ENST00000449557.6:c.5159_5160delinsAC	ENSP00000413996.2:p.Asn1720=
ENST00000450102.6:c.5159_5160delinsAC	ENSP00000403355.2:p.Asn1720=
ENST00000451551.6:c.5159_5160delinsAC	ENSP00000388797.2:p.Asn1720=
ENST00000455624.6:c.5222_5223delinsAC	ENSP00000399524.2:p.Asn1741=
NM_000335.4:c.5318_5319delinsAC , LRG_289t2:c.5318_5319delinsAC	NP_000326.2:p.Asn1773=
NM_001099404.1:c.5321_5322delinsAC , LRG_289t3:c.5321_5322delinsAC	NP_001092874.1:p.Asn1774=
NM_001099405.1:c.5267_5268delinsAC	NP_001092875.1:p.Asn1756=
NM_001160160.1:c.5222_5223delinsAC	NP_001153632.1:p.Asn1741=
NM_001160161.1:c.5159_5160delinsAC	NP_001153633.1:p.Asn1720=
NM_198056.2:c.5321_5322delinsAC , LRG_289t1:c.5321_5322delinsAC	NP_932173.1:p.Asn1774=
XM_006713282.2:c.5321_5322delinsAC	XP_006713345.1:p.Asn1774=
XM_011533991.1:c.5318_5319delinsAC	XP_011532293.1:p.Asn1773=
XM_011533992.1:c.5192_5193delinsAC	XP_011532294.1:p.Asn1731=
NM_001354701.1:c.5264_5265delinsAC	NP_001341630.1:p.Asn1755=
XM_011533991.2:c.5318_5319delinsAC	XP_011532293.1:p.Asn1773=
XM_017007017.1:c.5159_5160delinsAC	XP_016862506.1:p.Asn1720=
NM_000335.5:c.5318_5319delinsAC MANE Select	NP_000326.2:p.Asn1773=
NM_001160160.2:c.5222_5223delinsAC	NP_001153632.1:p.Asn1741=
NM_001354701.2:c.5264_5265delinsAC	NP_001341630.1:p.Asn1755=
NM_001099404.2:c.5321_5322delinsAC MANE Plus Clinical	NP_001092874.1:p.Asn1774=
NM_001099405.2:c.5267_5268delinsAC	NP_001092875.1:p.Asn1756=
NM_001160161.2:c.5159_5160delinsAC	NP_001153633.1:p.Asn1720=
NM_198056.3:c.5321_5322delinsAC	NP_932173.1:p.Asn1774=