Canonical Allele Identifier: CA1546666349

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658731A= , CM000667.2:g.53658731A=	GRCh38
NC_000005.9:g.52954561A= , CM000667.1:g.52954561A=	GRCh37
NC_000005.8:g.52990318A=	NCBI36
NG_008200.1:g.103097A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.424+107A= MANE Select	ENSP00000296684.5:n.424+107A=
ENST00000296684.9:c.424+107A=	ENSP00000296684.5:n.424+107A=
ENST00000502423.5:c.*291+107A=	ENSP00000422177.1:n.*291+107A=
ENST00000506765.1:c.338+12326A=	ENSP00000424570.1:n.338+12326A=
ENST00000506974.5:c.*200+107A=	ENSP00000425967.1:n.*200+107A=
ENST00000507026.5:c.*398+107A=	ENSP00000424993.1:n.*398+107A=
ENST00000509443.1:n.392A=
NM_002495.2:c.424+107A=	NP_002486.1:n.424+107A=
XM_005248525.3:c.350+12326A=	XP_005248582.1:n.350+12326A=
XM_011543415.1:c.250+107A=	XP_011541717.1:n.250+107A=
NM_001318051.1:c.350+12326A=	NP_001304980.1:n.350+12326A=
NM_002495.3:c.424+107A=	NP_002486.1:n.424+107A=
NR_134473.1:n.626+107A=
NR_134474.1:n.543+107A=
NR_134475.1:n.578+107A=
NM_002495.4:c.424+107A= MANE Select	NP_002486.1:n.424+107A=
NM_001318051.2:c.350+12326A=	NP_001304980.1:n.350+12326A=
NR_134473.2:n.620+107A=
NR_134474.2:n.537+107A=
NR_134475.2:n.572+107A=