Canonical Allele Identifier: CA1546666296

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658609T= , CM000667.2:g.53658609T=	GRCh38
NC_000005.9:g.52954439T= , CM000667.1:g.52954439T=	GRCh37
NC_000005.8:g.52990196T=	NCBI36
NG_008200.1:g.102975T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.409T= MANE Select	ENSP00000296684.5:p.Phe137=
ENST00000296684.9:c.409T=	ENSP00000296684.5:p.Phe137=
ENST00000502423.5:c.*276T=	ENSP00000422177.1:n.*276T=
ENST00000506765.1:c.338+12204T=	ENSP00000424570.1:n.338+12204T=
ENST00000506974.5:c.*185T=	ENSP00000425967.1:n.*185T=
ENST00000507026.5:c.*383T=	ENSP00000424993.1:n.*383T=
ENST00000509443.1:n.270T=
NM_002495.2:c.409T=	NP_002486.1:p.Phe137=
XM_005248525.3:c.350+12204T=	XP_005248582.1:n.350+12204T=
XM_011543415.1:c.235T=	XP_011541717.1:p.Phe79=
NM_001318051.1:c.350+12204T=	NP_001304980.1:n.350+12204T=
NM_002495.3:c.409T=	NP_002486.1:p.Phe137=
NR_134473.1:n.611T=
NR_134474.1:n.528T=
NR_134475.1:n.563T=
NM_002495.4:c.409T= MANE Select	NP_002486.1:p.Phe137=
NM_001318051.2:c.350+12204T=	NP_001304980.1:n.350+12204T=
NR_134473.2:n.605T=
NR_134474.2:n.522T=
NR_134475.2:n.557T=