Canonical Allele Identifier: CA1546660842

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646317C= , CM000667.2:g.53646317C=	GRCh38
NC_000005.9:g.52942147C= , CM000667.1:g.52942147C=	GRCh37
NC_000005.8:g.52977904C=	NCBI36
NG_008200.1:g.90683C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.262C= MANE Select	ENSP00000296684.5:p.Gln88=
ENST00000296684.9:c.262C=	ENSP00000296684.5:p.Gln88=
ENST00000502423.5:c.*129C=	ENSP00000422177.1:n.*129C=
ENST00000506765.1:c.250C=	ENSP00000424570.1:p.Gln84=
ENST00000506974.5:c.*38C=	ENSP00000425967.1:n.*38C=
ENST00000507026.5:c.*236C=	ENSP00000424993.1:n.*236C=
ENST00000509443.1:n.123C=
NM_002495.2:c.262C=	NP_002486.1:p.Gln88=
XM_005248525.3:c.262C=	XP_005248582.1:p.Gln88=
XM_011543415.1:c.88C=	XP_011541717.1:p.Gln30=
NM_001318051.1:c.262C=	NP_001304980.1:p.Gln88=
NM_002495.3:c.262C=	NP_002486.1:p.Gln88=
NR_134473.1:n.464C=
NR_134474.1:n.381C=
NR_134475.1:n.416C=
NM_002495.4:c.262C= MANE Select	NP_002486.1:p.Gln88=
NM_001318051.2:c.262C=	NP_001304980.1:p.Gln88=
NR_134473.2:n.458C=
NR_134474.2:n.375C=
NR_134475.2:n.410C=