Canonical Allele Identifier: CA1546660823

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646260G= , CM000667.2:g.53646260G=	GRCh38
NC_000005.9:g.52942090G= , CM000667.1:g.52942090G=	GRCh37
NC_000005.8:g.52977847G=	NCBI36
NG_008200.1:g.90626G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.205G= MANE Select	ENSP00000296684.5:p.Glu69=
ENST00000296684.9:c.205G=	ENSP00000296684.5:p.Glu69=
ENST00000502423.5:c.*72G=	ENSP00000422177.1:n.*72G=
ENST00000506765.1:c.193G=	ENSP00000424570.1:p.Glu65=
ENST00000506974.5:c.377G=	ENSP00000425967.1:p.Arg126=
ENST00000507026.5:c.*179G=	ENSP00000424993.1:n.*179G=
ENST00000509443.1:n.66G=
NM_002495.2:c.205G=	NP_002486.1:p.Glu69=
XM_005248525.3:c.205G=	XP_005248582.1:p.Glu69=
XM_011543415.1:c.31G=	XP_011541717.1:p.Glu11=
NM_001318051.1:c.205G=	NP_001304980.1:p.Glu69=
NM_002495.3:c.205G=	NP_002486.1:p.Glu69=
NR_134473.1:n.407G=
NR_134474.1:n.324G=
NR_134475.1:n.359G=
NM_002495.4:c.205G= MANE Select	NP_002486.1:p.Glu69=
NM_001318051.2:c.205G=	NP_001304980.1:p.Glu69=
NR_134473.2:n.401G=
NR_134474.2:n.318G=
NR_134475.2:n.353G=