Canonical Allele Identifier: CA1358558284

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551515_38551516delinsCG , CM000665.2:g.38551515_38551516delinsCG	GRCh38
NC_000003.11:g.38593006_38593007delinsCG , CM000665.1:g.38593006_38593007delinsCG	GRCh37
NC_000003.10:g.38568010_38568011delinsCG	NCBI36
NG_008934.1:g.103157_103158delinsCG , LRG_289:g.103157_103158delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.4853_4854delinsCG	ENSP00000333674.7:p.Pro1618=
ENST00000333535.9:c.4856_4857delinsCG	ENSP00000328968.4:p.Pro1619=
ENST00000413689.6:c.4856_4857delinsCG MANE Plus Clinical	ENSP00000410257.1:p.Pro1619=
ENST00000423572.7:c.4853_4854delinsCG MANE Select	ENSP00000398266.2:p.Pro1618=
ENST00000333535.8:c.4856_4857delinsCG	ENSP00000328968.4:p.Pro1619=
ENST00000413689.5:c.4856_4857delinsCG	ENSP00000410257.1:p.Pro1619=
ENST00000414099.6:c.4802_4803delinsCG	ENSP00000398962.2:p.Pro1601=
ENST00000423572.6:c.4853_4854delinsCG	ENSP00000398266.2:p.Pro1618=
ENST00000425664.5:c.4802_4803delinsCG	ENSP00000416634.1:p.Pro1601=
ENST00000449557.6:c.4694_4695delinsCG	ENSP00000413996.2:p.Pro1565=
ENST00000450102.6:c.4694_4695delinsCG	ENSP00000403355.2:p.Pro1565=
ENST00000451551.6:c.4694_4695delinsCG	ENSP00000388797.2:p.Pro1565=
ENST00000455624.6:c.4757_4758delinsCG	ENSP00000399524.2:p.Pro1586=
NM_000335.4:c.4853_4854delinsCG , LRG_289t2:c.4853_4854delinsCG	NP_000326.2:p.Pro1618=
NM_001099404.1:c.4856_4857delinsCG , LRG_289t3:c.4856_4857delinsCG	NP_001092874.1:p.Pro1619=
NM_001099405.1:c.4802_4803delinsCG	NP_001092875.1:p.Pro1601=
NM_001160160.1:c.4757_4758delinsCG	NP_001153632.1:p.Pro1586=
NM_001160161.1:c.4694_4695delinsCG	NP_001153633.1:p.Pro1565=
NM_198056.2:c.4856_4857delinsCG , LRG_289t1:c.4856_4857delinsCG	NP_932173.1:p.Pro1619=
XM_006713282.2:c.4856_4857delinsCG	XP_006713345.1:p.Pro1619=
XM_011533991.1:c.4853_4854delinsCG	XP_011532293.1:p.Pro1618=
XM_011533992.1:c.4727_4728delinsCG	XP_011532294.1:p.Pro1576=
NM_001354701.1:c.4799_4800delinsCG	NP_001341630.1:p.Pro1600=
XM_011533991.2:c.4853_4854delinsCG	XP_011532293.1:p.Pro1618=
XM_017007017.1:c.4694_4695delinsCG	XP_016862506.1:p.Pro1565=
NM_000335.5:c.4853_4854delinsCG MANE Select	NP_000326.2:p.Pro1618=
NM_001160160.2:c.4757_4758delinsCG	NP_001153632.1:p.Pro1586=
NM_001354701.2:c.4799_4800delinsCG	NP_001341630.1:p.Pro1600=
NM_001099404.2:c.4856_4857delinsCG MANE Plus Clinical	NP_001092874.1:p.Pro1619=
NM_001099405.2:c.4802_4803delinsCG	NP_001092875.1:p.Pro1601=
NM_001160161.2:c.4694_4695delinsCG	NP_001153633.1:p.Pro1565=
NM_198056.3:c.4856_4857delinsCG	NP_932173.1:p.Pro1619=