Canonical Allele Identifier: CA1358557150

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551007_38551011delinsCCTCA , CM000665.2:g.38551007_38551011delinsCCTCA	GRCh38
NC_000003.11:g.38592498_38592502delinsCCTCA , CM000665.1:g.38592498_38592502delinsCCTCA	GRCh37
NC_000003.10:g.38567502_38567506delinsCCTCA	NCBI36
NG_008934.1:g.103662_103666delinsTGAGG , LRG_289:g.103662_103666delinsTGAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000327956.7:c.5358_5362delinsTGAGG	ENSP00000333674.7:p.Ser1786=
ENST00000333535.9:c.5361_5365delinsTGAGG	ENSP00000328968.4:p.Ser1787=
ENST00000413689.6:c.5361_5365delinsTGAGG MANE Plus Clinical	ENSP00000410257.1:p.Ser1787=
ENST00000423572.7:c.5358_5362delinsTGAGG MANE Select	ENSP00000398266.2:p.Ser1786=
ENST00000333535.8:c.5361_5365delinsTGAGG	ENSP00000328968.4:p.Ser1787=
ENST00000413689.5:c.5361_5365delinsTGAGG	ENSP00000410257.1:p.Ser1787=
ENST00000414099.6:c.5307_5311delinsTGAGG	ENSP00000398962.2:p.Ser1769=
ENST00000423572.6:c.5358_5362delinsTGAGG	ENSP00000398266.2:p.Ser1786=
ENST00000425664.5:c.5307_5311delinsTGAGG	ENSP00000416634.1:p.Ser1769=
ENST00000449557.6:c.5199_5203delinsTGAGG	ENSP00000413996.2:p.Ser1733=
ENST00000450102.6:c.5199_5203delinsTGAGG	ENSP00000403355.2:p.Ser1733=
ENST00000451551.6:c.5199_5203delinsTGAGG	ENSP00000388797.2:p.Ser1733=
ENST00000455624.6:c.5262_5266delinsTGAGG	ENSP00000399524.2:p.Ser1754=
NM_000335.4:c.5358_5362delinsTGAGG , LRG_289t2:c.5358_5362delinsTGAGG	NP_000326.2:p.Ser1786=
NM_001099404.1:c.5361_5365delinsTGAGG , LRG_289t3:c.5361_5365delinsTGAGG	NP_001092874.1:p.Ser1787=
NM_001099405.1:c.5307_5311delinsTGAGG	NP_001092875.1:p.Ser1769=
NM_001160160.1:c.5262_5266delinsTGAGG	NP_001153632.1:p.Ser1754=
NM_001160161.1:c.5199_5203delinsTGAGG	NP_001153633.1:p.Ser1733=
NM_198056.2:c.5361_5365delinsTGAGG , LRG_289t1:c.5361_5365delinsTGAGG	NP_932173.1:p.Ser1787=
XM_006713282.2:c.5361_5365delinsTGAGG	XP_006713345.1:p.Ser1787=
XM_011533991.1:c.5358_5362delinsTGAGG	XP_011532293.1:p.Ser1786=
XM_011533992.1:c.5232_5236delinsTGAGG	XP_011532294.1:p.Ser1744=
NM_001354701.1:c.5304_5308delinsTGAGG	NP_001341630.1:p.Ser1768=
XM_011533991.2:c.5358_5362delinsTGAGG	XP_011532293.1:p.Ser1786=
XM_017007017.1:c.5199_5203delinsTGAGG	XP_016862506.1:p.Ser1733=
NM_000335.5:c.5358_5362delinsTGAGG MANE Select	NP_000326.2:p.Ser1786=
NM_001160160.2:c.5262_5266delinsTGAGG	NP_001153632.1:p.Ser1754=
NM_001354701.2:c.5304_5308delinsTGAGG	NP_001341630.1:p.Ser1768=
NM_001099404.2:c.5361_5365delinsTGAGG MANE Plus Clinical	NP_001092874.1:p.Ser1787=
NM_001099405.2:c.5307_5311delinsTGAGG	NP_001092875.1:p.Ser1769=
NM_001160161.2:c.5199_5203delinsTGAGG	NP_001153633.1:p.Ser1733=
NM_198056.3:c.5361_5365delinsTGAGG	NP_932173.1:p.Ser1787=