Canonical Allele Identifier: CA1546660824

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646264A= , CM000667.2:g.53646264A=	GRCh38
NC_000005.9:g.52942094A= , CM000667.1:g.52942094A=	GRCh37
NC_000005.8:g.52977851A=	NCBI36
NG_008200.1:g.90630A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.209A= MANE Select	ENSP00000296684.5:p.Glu70=
ENST00000296684.9:c.209A=	ENSP00000296684.5:p.Glu70=
ENST00000502423.5:c.*76A=	ENSP00000422177.1:n.*76A=
ENST00000506765.1:c.197A=	ENSP00000424570.1:p.Glu66=
ENST00000506974.5:c.381A=	ENSP00000425967.1:p.Arg127=
ENST00000507026.5:c.*183A=	ENSP00000424993.1:n.*183A=
ENST00000509443.1:n.70A=
NM_002495.2:c.209A=	NP_002486.1:p.Glu70=
XM_005248525.3:c.209A=	XP_005248582.1:p.Glu70=
XM_011543415.1:c.35A=	XP_011541717.1:p.Glu12=
NM_001318051.1:c.209A=	NP_001304980.1:p.Glu70=
NM_002495.3:c.209A=	NP_002486.1:p.Glu70=
NR_134473.1:n.411A=
NR_134474.1:n.328A=
NR_134475.1:n.363A=
NM_002495.4:c.209A= MANE Select	NP_002486.1:p.Glu70=
NM_001318051.2:c.209A=	NP_001304980.1:p.Glu70=
NR_134473.2:n.405A=
NR_134474.2:n.322A=
NR_134475.2:n.357A=