Canonical Allele Identifier: CA1358584394

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38603444_38603445delinsAG , CM000665.2:g.38603444_38603445delinsAG	GRCh38
NC_000003.11:g.38644935_38644936delinsAG , CM000665.1:g.38644935_38644936delinsAG	GRCh37
NC_000003.10:g.38619939_38619940delinsAG	NCBI36
NG_008934.1:g.51228_51229delinsCT , LRG_289:g.51228_51229delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.1890+267_1890+268delinsCT	ENSP00000333674.7:n.1890+267_1890+268delinsCT
ENST00000333535.9:c.1890+267_1890+268delinsCT	ENSP00000328968.4:n.1890+267_1890+268delinsCT
ENST00000413689.6:c.1890+267_1890+268delinsCT MANE Plus Clinical	ENSP00000410257.1:n.1890+267_1890+268delinsCT
ENST00000423572.7:c.1890+267_1890+268delinsCT MANE Select	ENSP00000398266.2:n.1890+267_1890+268delinsCT
ENST00000333535.8:c.1890+267_1890+268delinsCT	ENSP00000328968.4:n.1890+267_1890+268delinsCT
ENST00000413689.5:c.1890+267_1890+268delinsCT	ENSP00000410257.1:n.1890+267_1890+268delinsCT
ENST00000414099.6:c.1890+267_1890+268delinsCT	ENSP00000398962.2:n.1890+267_1890+268delinsCT
ENST00000423572.6:c.1890+267_1890+268delinsCT	ENSP00000398266.2:n.1890+267_1890+268delinsCT
ENST00000425664.5:c.1890+267_1890+268delinsCT	ENSP00000416634.1:n.1890+267_1890+268delinsCT
ENST00000449557.6:c.1890+267_1890+268delinsCT	ENSP00000413996.2:n.1890+267_1890+268delinsCT
ENST00000450102.6:c.1890+267_1890+268delinsCT	ENSP00000403355.2:n.1890+267_1890+268delinsCT
ENST00000451551.6:c.1890+267_1890+268delinsCT	ENSP00000388797.2:n.1890+267_1890+268delinsCT
ENST00000455624.6:c.1890+267_1890+268delinsCT	ENSP00000399524.2:n.1890+267_1890+268delinsCT
NM_000335.4:c.1890+267_1890+268delinsCT , LRG_289t2:c.1890+267_1890+268delinsCT	NP_000326.2:n.1890+267_1890+268delinsCT
NM_001099404.1:c.1890+267_1890+268delinsCT , LRG_289t3:c.1890+267_1890+268delinsCT	NP_001092874.1:n.1890+267_1890+268delinsCT
NM_001099405.1:c.1890+267_1890+268delinsCT	NP_001092875.1:n.1890+267_1890+268delinsCT
NM_001160160.1:c.1890+267_1890+268delinsCT	NP_001153632.1:n.1890+267_1890+268delinsCT
NM_001160161.1:c.1890+267_1890+268delinsCT	NP_001153633.1:n.1890+267_1890+268delinsCT
NM_198056.2:c.1890+267_1890+268delinsCT , LRG_289t1:c.1890+267_1890+268delinsCT	NP_932173.1:n.1890+267_1890+268delinsCT
XM_006713282.2:c.1890+267_1890+268delinsCT	XP_006713345.1:n.1890+267_1890+268delinsCT
XM_011533991.1:c.1890+267_1890+268delinsCT	XP_011532293.1:n.1890+267_1890+268delinsCT
XM_011533992.1:c.1761+267_1761+268delinsCT	XP_011532294.1:n.1761+267_1761+268delinsCT
NM_001354701.1:c.1890+267_1890+268delinsCT	NP_001341630.1:n.1890+267_1890+268delinsCT
XM_011533991.2:c.1890+267_1890+268delinsCT	XP_011532293.1:n.1890+267_1890+268delinsCT
XM_017007017.1:c.1890+267_1890+268delinsCT	XP_016862506.1:n.1890+267_1890+268delinsCT
NM_000335.5:c.1890+267_1890+268delinsCT MANE Select	NP_000326.2:n.1890+267_1890+268delinsCT
NM_001160160.2:c.1890+267_1890+268delinsCT	NP_001153632.1:n.1890+267_1890+268delinsCT
NM_001354701.2:c.1890+267_1890+268delinsCT	NP_001341630.1:n.1890+267_1890+268delinsCT
NM_001099404.2:c.1890+267_1890+268delinsCT MANE Plus Clinical	NP_001092874.1:n.1890+267_1890+268delinsCT
NM_001099405.2:c.1890+267_1890+268delinsCT	NP_001092875.1:n.1890+267_1890+268delinsCT
NM_001160161.2:c.1890+267_1890+268delinsCT	NP_001153633.1:n.1890+267_1890+268delinsCT
NM_198056.3:c.1890+267_1890+268delinsCT	NP_932173.1:n.1890+267_1890+268delinsCT