Canonical Allele Identifier: CA1046986960

Gene: SCN5A

Linked Data

• gnomAD v3: 3-38551525-A-AG
• gnomAD v4: 3-38551525-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551525_38551526insG , CM000665.2:g.38551525_38551526insG	GRCh38
NC_000003.11:g.38593016_38593017insG , CM000665.1:g.38593016_38593017insG	GRCh37
NC_000003.10:g.38568020_38568021insG	NCBI36
NG_008934.1:g.103147_103148insC , LRG_289:g.103147_103148insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4843_4844insC	ENSP00000333674.7:p.Phe1615SerfsTer?
ENST00000333535.9:c.4846_4847insC	ENSP00000328968.4:p.Phe1616SerfsTer?
ENST00000413689.6:c.4846_4847insC MANE Plus Clinical	ENSP00000410257.1:p.Phe1616SerfsTer?
ENST00000423572.7:c.4843_4844insC MANE Select	ENSP00000398266.2:p.Phe1615SerfsTer?
ENST00000333535.8:c.4846_4847insC	ENSP00000328968.4:p.Phe1616SerfsTer?
ENST00000413689.5:c.4846_4847insC	ENSP00000410257.1:p.Phe1616SerfsTer?
ENST00000414099.6:c.4792_4793insC	ENSP00000398962.2:p.Phe1598SerfsTer?
ENST00000423572.6:c.4843_4844insC	ENSP00000398266.2:p.Phe1615SerfsTer?
ENST00000425664.5:c.4792_4793insC	ENSP00000416634.1:p.Phe1598SerfsTer?
ENST00000449557.6:c.4684_4685insC	ENSP00000413996.2:p.Phe1562SerfsTer?
ENST00000450102.6:c.4684_4685insC	ENSP00000403355.2:p.Phe1562SerfsTer?
ENST00000451551.6:c.4684_4685insC	ENSP00000388797.2:p.Phe1562SerfsTer?
ENST00000455624.6:c.4747_4748insC	ENSP00000399524.2:p.Phe1583SerfsTer?
NM_000335.4:c.4843_4844insC , LRG_289t2:c.4843_4844insC	NP_000326.2:p.Phe1615SerfsTer?
NM_001099404.1:c.4846_4847insC , LRG_289t3:c.4846_4847insC	NP_001092874.1:p.Phe1616SerfsTer?
NM_001099405.1:c.4792_4793insC	NP_001092875.1:p.Phe1598SerfsTer?
NM_001160160.1:c.4747_4748insC	NP_001153632.1:p.Phe1583SerfsTer?
NM_001160161.1:c.4684_4685insC	NP_001153633.1:p.Phe1562SerfsTer?
NM_198056.2:c.4846_4847insC , LRG_289t1:c.4846_4847insC	NP_932173.1:p.Phe1616SerfsTer?
XM_006713282.2:c.4846_4847insC	XP_006713345.1:p.Phe1616SerfsTer?
XM_011533991.1:c.4843_4844insC	XP_011532293.1:p.Phe1615SerfsTer?
XM_011533992.1:c.4717_4718insC	XP_011532294.1:p.Phe1573SerfsTer?
NM_001354701.1:c.4789_4790insC	NP_001341630.1:p.Phe1597SerfsTer?
XM_011533991.2:c.4843_4844insC	XP_011532293.1:p.Phe1615SerfsTer?
XM_017007017.1:c.4684_4685insC	XP_016862506.1:p.Phe1562SerfsTer?
NM_000335.5:c.4843_4844insC MANE Select	NP_000326.2:p.Phe1615SerfsTer?
NM_001160160.2:c.4747_4748insC	NP_001153632.1:p.Phe1583SerfsTer?
NM_001354701.2:c.4789_4790insC	NP_001341630.1:p.Phe1597SerfsTer?
NM_001099404.2:c.4846_4847insC MANE Plus Clinical	NP_001092874.1:p.Phe1616SerfsTer?
NM_001099405.2:c.4792_4793insC	NP_001092875.1:p.Phe1598SerfsTer?
NM_001160161.2:c.4684_4685insC	NP_001153633.1:p.Phe1562SerfsTer?
NM_198056.3:c.4846_4847insC	NP_932173.1:p.Phe1616SerfsTer?