Canonical Allele Identifier: CA1546620702

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560689A= , CM000667.2:g.53560689A=	GRCh38
NC_000005.9:g.52856519A= , CM000667.1:g.52856519A=	GRCh37
NC_000005.8:g.52892276A=	NCBI36
NG_008200.1:g.5055A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.27A= MANE Select	ENSP00000296684.5:p.Val9=
ENST00000296684.9:c.27A=	ENSP00000296684.5:p.Val9=
ENST00000502423.5:c.27A=	ENSP00000422177.1:p.Val9=
ENST00000506765.1:c.15A=	ENSP00000424570.1:p.Val5=
ENST00000506974.5:c.27A=	ENSP00000425967.1:p.Val9=
ENST00000507026.5:c.27A=	ENSP00000424993.1:p.Val9=
NM_002495.2:c.27A=	NP_002486.1:p.Val9=
XM_005248525.3:c.27A=	XP_005248582.1:p.Val9=
XM_011543414.1:c.27A=	XP_011541716.1:p.Val9=
NM_001318051.1:c.27A=	NP_001304980.1:p.Val9=
NM_002495.3:c.27A=	NP_002486.1:p.Val9=
NR_134473.1:n.57A=
NR_134474.1:n.57A=
NR_134475.1:n.57A=
XM_017009491.1:c.27A=	XP_016864980.1:p.Val9=
NM_002495.4:c.27A= MANE Select	NP_002486.1:p.Val9=
NM_001318051.2:c.27A=	NP_001304980.1:p.Val9=
NR_134473.2:n.51A=
NR_134474.2:n.51A=
NR_134475.2:n.51A=