Canonical Allele Identifier: CA1546666291

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658593A= , CM000667.2:g.53658593A=	GRCh38
NC_000005.9:g.52954423A= , CM000667.1:g.52954423A=	GRCh37
NC_000005.8:g.52990180A=	NCBI36
NG_008200.1:g.102959A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.393A= MANE Select	ENSP00000296684.5:p.Lys131=
ENST00000296684.9:c.393A=	ENSP00000296684.5:p.Lys131=
ENST00000502423.5:c.*260A=	ENSP00000422177.1:n.*260A=
ENST00000506765.1:c.338+12188A=	ENSP00000424570.1:n.338+12188A=
ENST00000506974.5:c.*169A=	ENSP00000425967.1:n.*169A=
ENST00000507026.5:c.*367A=	ENSP00000424993.1:n.*367A=
ENST00000509443.1:n.254A=
NM_002495.2:c.393A=	NP_002486.1:p.Lys131=
XM_005248525.3:c.350+12188A=	XP_005248582.1:n.350+12188A=
XM_011543415.1:c.219A=	XP_011541717.1:p.Lys73=
NM_001318051.1:c.350+12188A=	NP_001304980.1:n.350+12188A=
NM_002495.3:c.393A=	NP_002486.1:p.Lys131=
NR_134473.1:n.595A=
NR_134474.1:n.512A=
NR_134475.1:n.547A=
NM_002495.4:c.393A= MANE Select	NP_002486.1:p.Lys131=
NM_001318051.2:c.350+12188A=	NP_001304980.1:n.350+12188A=
NR_134473.2:n.589A=
NR_134474.2:n.506A=
NR_134475.2:n.541A=