Canonical Allele Identifier: CA1546660825

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646267A= , CM000667.2:g.53646267A=	GRCh38
NC_000005.9:g.52942097A= , CM000667.1:g.52942097A=	GRCh37
NC_000005.8:g.52977854A=	NCBI36
NG_008200.1:g.90633A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.212A= MANE Select	ENSP00000296684.5:p.His71=
ENST00000296684.9:c.212A=	ENSP00000296684.5:p.His71=
ENST00000502423.5:c.*79A=	ENSP00000422177.1:n.*79A=
ENST00000506765.1:c.200A=	ENSP00000424570.1:p.His67=
ENST00000506974.5:c.384A=	ENSP00000425967.1:p.Ala128=
ENST00000507026.5:c.*186A=	ENSP00000424993.1:n.*186A=
ENST00000509443.1:n.73A=
NM_002495.2:c.212A=	NP_002486.1:p.His71=
XM_005248525.3:c.212A=	XP_005248582.1:p.His71=
XM_011543415.1:c.38A=	XP_011541717.1:p.His13=
NM_001318051.1:c.212A=	NP_001304980.1:p.His71=
NM_002495.3:c.212A=	NP_002486.1:p.His71=
NR_134473.1:n.414A=
NR_134474.1:n.331A=
NR_134475.1:n.366A=
NM_002495.4:c.212A= MANE Select	NP_002486.1:p.His71=
NM_001318051.2:c.212A=	NP_001304980.1:p.His71=
NR_134473.2:n.408A=
NR_134474.2:n.325A=
NR_134475.2:n.360A=