Canonical Allele Identifier: CA1358555934
Community Standard Title: NM_000335.5(SCN5A):c.5848G= (p.Val1950=)
Gene: SCN5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38550521C= , CM000665.2:g.38550521C= GRCh38
NC_000003.11:g.38592012C= , CM000665.1:g.38592012C= GRCh37
NC_000003.10:g.38567016C= NCBI36
NG_008934.1:g.104152G= , LRG_289:g.104152G=

Transcript Alleles

HGVS Amino-acid Change
NM_000335.5:c.5848G= MANE Select NP_000326.2:p.Val1950=
ENST00000423572.7:c.5848G= MANE Select ENSP00000398266.2:p.Val1950=
NM_001099404.2:c.5851G= MANE Plus Clinical NP_001092874.1:p.Val1951=
ENST00000413689.6:c.5851G= MANE Plus Clinical ENSP00000410257.1:p.Val1951=
NM_000335.4:c.5848G= , LRG_289t2:c.5848G= NP_000326.2:p.Val1950=
NM_001099404.1:c.5851G= , LRG_289t3:c.5851G= NP_001092874.1:p.Val1951=
NM_001099405.1:c.5797G= NP_001092875.1:p.Val1933=
NM_001099405.2:c.5797G= NP_001092875.1:p.Val1933=
NM_001160160.1:c.5752G= NP_001153632.1:p.Val1918=
NM_001160160.2:c.5752G= NP_001153632.1:p.Val1918=
NM_001160161.1:c.5689G= NP_001153633.1:p.Val1897=
NM_001160161.2:c.5689G= NP_001153633.1:p.Val1897=
NM_001354701.1:c.5794G= NP_001341630.1:p.Val1932=
NM_001354701.2:c.5794G= NP_001341630.1:p.Val1932=
NM_198056.2:c.5851G= , LRG_289t1:c.5851G= NP_932173.1:p.Val1951=
NM_198056.3:c.5851G= NP_932173.1:p.Val1951=
ENST00000327956.7:c.5848G= ENSP00000333674.7:p.Val1950=
ENST00000333535.8:c.5851G= ENSP00000328968.4:p.Val1951=
ENST00000333535.9:c.5851G= ENSP00000328968.4:p.Val1951=
ENST00000413689.5:c.5851G= ENSP00000410257.1:p.Val1951=
ENST00000414099.6:c.5797G= ENSP00000398962.2:p.Val1933=
ENST00000423572.6:c.5848G= ENSP00000398266.2:p.Val1950=
ENST00000425664.5:c.5797G= ENSP00000416634.1:p.Val1933=
ENST00000449557.6:c.5689G= ENSP00000413996.2:p.Val1897=
ENST00000450102.6:c.5689G= ENSP00000403355.2:p.Val1897=
ENST00000451551.6:c.5689G= ENSP00000388797.2:p.Val1897=
ENST00000455624.6:c.5752G= ENSP00000399524.2:p.Val1918=
XM_006713282.2:c.5851G= XP_006713345.1:p.Val1951=
XM_011533991.1:c.5848G= XP_011532293.1:p.Val1950=
XM_011533991.2:c.5848G= XP_011532293.1:p.Val1950=
XM_011533992.1:c.5722G= XP_011532294.1:p.Val1908=
XM_017007017.1:c.5689G= XP_016862506.1:p.Val1897=