Canonical Allele Identifier: CA1546620665

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560647G= , CM000667.2:g.53560647G=	GRCh38
NC_000005.9:g.52856477G= , CM000667.1:g.52856477G=	GRCh37
NC_000005.8:g.52892234G=	NCBI36
NG_008200.1:g.5013G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.-16G= MANE Select	ENSP00000296684.5:n.-16G=
ENST00000296684.9:c.-16G=	ENSP00000296684.5:n.-16G=
ENST00000502423.5:c.-16G=	ENSP00000422177.1:n.-16G=
ENST00000506974.5:c.-16G=	ENSP00000425967.1:n.-16G=
ENST00000507026.5:c.-16G=	ENSP00000424993.1:n.-16G=
NM_002495.2:c.-16G=	NP_002486.1:n.-16G=
XM_005248525.3:c.-16G=	XP_005248582.1:n.-16G=
XM_011543414.1:c.-16G=	XP_011541716.1:n.-16G=
NM_001318051.1:c.-16G=	NP_001304980.1:n.-16G=
NM_002495.3:c.-16G=	NP_002486.1:n.-16G=
NR_134473.1:n.15G=
NR_134474.1:n.15G=
NR_134475.1:n.15G=
XM_017009491.1:c.-16G=	XP_016864980.1:n.-16G=
NM_002495.4:c.-16G= MANE Select	NP_002486.1:n.-16G=
NM_001318051.2:c.-16G=	NP_001304980.1:n.-16G=
NR_134473.2:n.9G=
NR_134474.2:n.9G=
NR_134475.2:n.9G=