Canonical Allele Identifier: CA1546666432

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658823T= , CM000667.2:g.53658823T=	GRCh38
NC_000005.9:g.52954653T= , CM000667.1:g.52954653T=	GRCh37
NC_000005.8:g.52990410T=	NCBI36
NG_008200.1:g.103189T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.424+199T= MANE Select	ENSP00000296684.5:n.424+199T=
ENST00000296684.9:c.424+199T=	ENSP00000296684.5:n.424+199T=
ENST00000502423.5:c.*291+199T=	ENSP00000422177.1:n.*291+199T=
ENST00000506765.1:c.338+12418T=	ENSP00000424570.1:n.338+12418T=
ENST00000506974.5:c.*200+199T=	ENSP00000425967.1:n.*200+199T=
ENST00000507026.5:c.*398+199T=	ENSP00000424993.1:n.*398+199T=
NM_002495.2:c.424+199T=	NP_002486.1:n.424+199T=
XM_005248525.3:c.350+12418T=	XP_005248582.1:n.350+12418T=
XM_011543415.1:c.250+199T=	XP_011541717.1:n.250+199T=
NM_001318051.1:c.350+12418T=	NP_001304980.1:n.350+12418T=
NM_002495.3:c.424+199T=	NP_002486.1:n.424+199T=
NR_134473.1:n.626+199T=
NR_134474.1:n.543+199T=
NR_134475.1:n.578+199T=
NM_002495.4:c.424+199T= MANE Select	NP_002486.1:n.424+199T=
NM_001318051.2:c.350+12418T=	NP_001304980.1:n.350+12418T=
NR_134473.2:n.620+199T=
NR_134474.2:n.537+199T=
NR_134475.2:n.572+199T=