Canonical Allele Identifier: CA2573332691

Gene: SCN5A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38551330_38551332del , CM000665.2:g.38551330_38551332del	GRCh38
NC_000003.11:g.38592821_38592823del , CM000665.1:g.38592821_38592823del	GRCh37
NC_000003.10:g.38567825_38567827del	NCBI36
NG_008934.1:g.103342_103344del , LRG_289:g.103342_103344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327956.7:c.5038_5040del	ENSP00000333674.7:p.Tyr1680del
ENST00000333535.9:c.5041_5043del	ENSP00000328968.4:p.Tyr1681del
ENST00000413689.6:c.5041_5043del MANE Plus Clinical	ENSP00000410257.1:p.Tyr1681del
ENST00000423572.7:c.5038_5040del MANE Select	ENSP00000398266.2:p.Tyr1680del
ENST00000333535.8:c.5041_5043del	ENSP00000328968.4:p.Tyr1681del
ENST00000413689.5:c.5041_5043del	ENSP00000410257.1:p.Tyr1681del
ENST00000414099.6:c.4987_4989del	ENSP00000398962.2:p.Tyr1663del
ENST00000423572.6:c.5038_5040del	ENSP00000398266.2:p.Tyr1680del
ENST00000425664.5:c.4987_4989del	ENSP00000416634.1:p.Tyr1663del
ENST00000449557.6:c.4879_4881del	ENSP00000413996.2:p.Tyr1627del
ENST00000450102.6:c.4879_4881del	ENSP00000403355.2:p.Tyr1627del
ENST00000451551.6:c.4879_4881del	ENSP00000388797.2:p.Tyr1627del
ENST00000455624.6:c.4942_4944del	ENSP00000399524.2:p.Tyr1648del
NM_000335.4:c.5038_5040del , LRG_289t2:c.5038_5040del	NP_000326.2:p.Tyr1680del
NM_001099404.1:c.5041_5043del , LRG_289t3:c.5041_5043del	NP_001092874.1:p.Tyr1681del
NM_001099405.1:c.4987_4989del	NP_001092875.1:p.Tyr1663del
NM_001160160.1:c.4942_4944del	NP_001153632.1:p.Tyr1648del
NM_001160161.1:c.4879_4881del	NP_001153633.1:p.Tyr1627del
NM_198056.2:c.5041_5043del , LRG_289t1:c.5041_5043del	NP_932173.1:p.Tyr1681del
XM_006713282.2:c.5041_5043del	XP_006713345.1:p.Tyr1681del
XM_011533991.1:c.5038_5040del	XP_011532293.1:p.Tyr1680del
XM_011533992.1:c.4912_4914del	XP_011532294.1:p.Tyr1638del
NM_001354701.1:c.4984_4986del	NP_001341630.1:p.Tyr1662del
XM_011533991.2:c.5038_5040del	XP_011532293.1:p.Tyr1680del
XM_017007017.1:c.4879_4881del	XP_016862506.1:p.Tyr1627del
NM_000335.5:c.5038_5040del MANE Select	NP_000326.2:p.Tyr1680del
NM_001160160.2:c.4942_4944del	NP_001153632.1:p.Tyr1648del
NM_001354701.2:c.4984_4986del	NP_001341630.1:p.Tyr1662del
NM_001099404.2:c.5041_5043del MANE Plus Clinical	NP_001092874.1:p.Tyr1681del
NM_001099405.2:c.4987_4989del	NP_001092875.1:p.Tyr1663del
NM_001160161.2:c.4879_4881del	NP_001153633.1:p.Tyr1627del
NM_198056.3:c.5041_5043del	NP_932173.1:p.Tyr1681del