Canonical Allele Identifier: CA1546666210
Gene: NDUFS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53658426C= , CM000667.2:g.53658426C= GRCh38
NC_000005.9:g.52954256C= , CM000667.1:g.52954256C= GRCh37
NC_000005.8:g.52990013C= NCBI36
NG_008200.1:g.102792C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.351-125C= MANE Select ENSP00000296684.5:n.351-125C=
ENST00000296684.9:c.351-125C= ENSP00000296684.5:n.351-125C=
ENST00000502423.5:c.*218-125C= ENSP00000422177.1:n.*218-125C=
ENST00000506765.1:c.338+12021C= ENSP00000424570.1:n.338+12021C=
ENST00000506974.5:c.*127-125C= ENSP00000425967.1:n.*127-125C=
ENST00000507026.5:c.*325-125C= ENSP00000424993.1:n.*325-125C=
ENST00000509443.1:n.212-125C=
NM_002495.2:c.351-125C= NP_002486.1:n.351-125C=
XM_005248525.3:c.350+12021C= XP_005248582.1:n.350+12021C=
XM_011543415.1:c.177-125C= XP_011541717.1:n.177-125C=
NM_001318051.1:c.350+12021C= NP_001304980.1:n.350+12021C=
NM_002495.3:c.351-125C= NP_002486.1:n.351-125C=
NR_134473.1:n.553-125C=
NR_134474.1:n.470-125C=
NR_134475.1:n.505-125C=
NM_002495.4:c.351-125C= MANE Select NP_002486.1:n.351-125C=
NM_001318051.2:c.350+12021C= NP_001304980.1:n.350+12021C=
NR_134473.2:n.547-125C=
NR_134474.2:n.464-125C=
NR_134475.2:n.499-125C=