Canonical Allele Identifier: CA1358557109
Gene: SCN5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38550997T= , CM000665.2:g.38550997T= GRCh38
NC_000003.11:g.38592488T= , CM000665.1:g.38592488T= GRCh37
NC_000003.10:g.38567492T= NCBI36
NG_008934.1:g.103676A= , LRG_289:g.103676A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327956.7:c.5372A= ENSP00000333674.7:p.Asp1791=
ENST00000333535.9:c.5375A= ENSP00000328968.4:p.Asp1792=
ENST00000413689.6:c.5375A= MANE Plus Clinical ENSP00000410257.1:p.Asp1792=
ENST00000423572.7:c.5372A= MANE Select ENSP00000398266.2:p.Asp1791=
ENST00000333535.8:c.5375A= ENSP00000328968.4:p.Asp1792=
ENST00000413689.5:c.5375A= ENSP00000410257.1:p.Asp1792=
ENST00000414099.6:c.5321A= ENSP00000398962.2:p.Asp1774=
ENST00000423572.6:c.5372A= ENSP00000398266.2:p.Asp1791=
ENST00000425664.5:c.5321A= ENSP00000416634.1:p.Asp1774=
ENST00000449557.6:c.5213A= ENSP00000413996.2:p.Asp1738=
ENST00000450102.6:c.5213A= ENSP00000403355.2:p.Asp1738=
ENST00000451551.6:c.5213A= ENSP00000388797.2:p.Asp1738=
ENST00000455624.6:c.5276A= ENSP00000399524.2:p.Asp1759=
NM_000335.4:c.5372A= , LRG_289t2:c.5372A= NP_000326.2:p.Asp1791=
NM_001099404.1:c.5375A= , LRG_289t3:c.5375A= NP_001092874.1:p.Asp1792=
NM_001099405.1:c.5321A= NP_001092875.1:p.Asp1774=
NM_001160160.1:c.5276A= NP_001153632.1:p.Asp1759=
NM_001160161.1:c.5213A= NP_001153633.1:p.Asp1738=
NM_198056.2:c.5375A= , LRG_289t1:c.5375A= NP_932173.1:p.Asp1792=
XM_006713282.2:c.5375A= XP_006713345.1:p.Asp1792=
XM_011533991.1:c.5372A= XP_011532293.1:p.Asp1791=
XM_011533992.1:c.5246A= XP_011532294.1:p.Asp1749=
NM_001354701.1:c.5318A= NP_001341630.1:p.Asp1773=
XM_011533991.2:c.5372A= XP_011532293.1:p.Asp1791=
XM_017007017.1:c.5213A= XP_016862506.1:p.Asp1738=
NM_000335.5:c.5372A= MANE Select NP_000326.2:p.Asp1791=
NM_001160160.2:c.5276A= NP_001153632.1:p.Asp1759=
NM_001354701.2:c.5318A= NP_001341630.1:p.Asp1773=
NM_001099404.2:c.5375A= MANE Plus Clinical NP_001092874.1:p.Asp1792=
NM_001099405.2:c.5321A= NP_001092875.1:p.Asp1774=
NM_001160161.2:c.5213A= NP_001153633.1:p.Asp1738=
NM_198056.3:c.5375A= NP_932173.1:p.Asp1792=