Canonical Allele Identifier: CA1546660832

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646289G= , CM000667.2:g.53646289G=	GRCh38
NC_000005.9:g.52942119G= , CM000667.1:g.52942119G=	GRCh37
NC_000005.8:g.52977876G=	NCBI36
NG_008200.1:g.90655G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.234G= MANE Select	ENSP00000296684.5:p.Arg78=
ENST00000296684.9:c.234G=	ENSP00000296684.5:p.Arg78=
ENST00000502423.5:c.*101G=	ENSP00000422177.1:n.*101G=
ENST00000506765.1:c.222G=	ENSP00000424570.1:p.Arg74=
ENST00000506974.5:c.*10G=	ENSP00000425967.1:n.*10G=
ENST00000507026.5:c.*208G=	ENSP00000424993.1:n.*208G=
ENST00000509443.1:n.95G=
NM_002495.2:c.234G=	NP_002486.1:p.Arg78=
XM_005248525.3:c.234G=	XP_005248582.1:p.Arg78=
XM_011543415.1:c.60G=	XP_011541717.1:p.Arg20=
NM_001318051.1:c.234G=	NP_001304980.1:p.Arg78=
NM_002495.3:c.234G=	NP_002486.1:p.Arg78=
NR_134473.1:n.436G=
NR_134474.1:n.353G=
NR_134475.1:n.388G=
NM_002495.4:c.234G= MANE Select	NP_002486.1:p.Arg78=
NM_001318051.2:c.234G=	NP_001304980.1:p.Arg78=
NR_134473.2:n.430G=
NR_134474.2:n.347G=
NR_134475.2:n.382G=