Canonical Allele Identifier: CA1546660853

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646336C= , CM000667.2:g.53646336C=	GRCh38
NC_000005.9:g.52942166C= , CM000667.1:g.52942166C=	GRCh37
NC_000005.8:g.52977923C=	NCBI36
NG_008200.1:g.90702C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.281C= MANE Select	ENSP00000296684.5:p.Thr94=
ENST00000296684.9:c.281C=	ENSP00000296684.5:p.Thr94=
ENST00000502423.5:c.*148C=	ENSP00000422177.1:n.*148C=
ENST00000506765.1:c.269C=	ENSP00000424570.1:p.Thr90=
ENST00000506974.5:c.*57C=	ENSP00000425967.1:n.*57C=
ENST00000507026.5:c.*255C=	ENSP00000424993.1:n.*255C=
ENST00000509443.1:n.142C=
NM_002495.2:c.281C=	NP_002486.1:p.Thr94=
XM_005248525.3:c.281C=	XP_005248582.1:p.Thr94=
XM_011543415.1:c.107C=	XP_011541717.1:p.Thr36=
NM_001318051.1:c.281C=	NP_001304980.1:p.Thr94=
NM_002495.3:c.281C=	NP_002486.1:p.Thr94=
NR_134473.1:n.483C=
NR_134474.1:n.400C=
NR_134475.1:n.435C=
NM_002495.4:c.281C= MANE Select	NP_002486.1:p.Thr94=
NM_001318051.2:c.281C=	NP_001304980.1:p.Thr94=
NR_134473.2:n.477C=
NR_134474.2:n.394C=
NR_134475.2:n.429C=