Canonical Allele Identifier: CA1546660870

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646371C= , CM000667.2:g.53646371C=	GRCh38
NC_000005.9:g.52942201C= , CM000667.1:g.52942201C=	GRCh37
NC_000005.8:g.52977958C=	NCBI36
NG_008200.1:g.90737C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296684.10:c.316C= MANE Select	ENSP00000296684.5:p.Arg106=
ENST00000296684.9:c.316C=	ENSP00000296684.5:p.Arg106=
ENST00000502423.5:c.*183C=	ENSP00000422177.1:n.*183C=
ENST00000506765.1:c.304C=	ENSP00000424570.1:p.Arg102=
ENST00000506974.5:c.*92C=	ENSP00000425967.1:n.*92C=
ENST00000507026.5:c.*290C=	ENSP00000424993.1:n.*290C=
ENST00000509443.1:n.177C=
NM_002495.2:c.316C=	NP_002486.1:p.Arg106=
XM_005248525.3:c.316C=	XP_005248582.1:p.Arg106=
XM_011543415.1:c.142C=	XP_011541717.1:p.Arg48=
NM_001318051.1:c.316C=	NP_001304980.1:p.Arg106=
NM_002495.3:c.316C=	NP_002486.1:p.Arg106=
NR_134473.1:n.518C=
NR_134474.1:n.435C=
NR_134475.1:n.470C=
NM_002495.4:c.316C= MANE Select	NP_002486.1:p.Arg106=
NM_001318051.2:c.316C=	NP_001304980.1:p.Arg106=
NR_134473.2:n.512C=
NR_134474.2:n.429C=
NR_134475.2:n.464C=