Canonical Allele Identifier: CA359719255
Gene: NDUFS4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53658618A>G , CM000667.2:g.53658618A>G GRCh38
NC_000005.9:g.52954448A>G , CM000667.1:g.52954448A>G GRCh37
NC_000005.8:g.52990205A>G NCBI36
NG_008200.1:g.102984A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.418A>G MANE Select ENSP00000296684.5:p.Lys140Glu
ENST00000296684.9:c.418A>G ENSP00000296684.5:p.Lys140Glu
ENST00000502423.5:c.*285A>G ENSP00000422177.1:n.*285A>G
ENST00000506765.1:c.338+12213A>G ENSP00000424570.1:n.338+12213A>G
ENST00000506974.5:c.*194A>G ENSP00000425967.1:n.*194A>G
ENST00000507026.5:c.*392A>G ENSP00000424993.1:n.*392A>G
ENST00000509443.1:n.279A>G
NM_002495.2:c.418A>G NP_002486.1:p.Lys140Glu
XM_005248525.3:c.350+12213A>G XP_005248582.1:n.350+12213A>G
XM_011543415.1:c.244A>G XP_011541717.1:p.Lys82Glu
NM_001318051.1:c.350+12213A>G NP_001304980.1:n.350+12213A>G
NM_002495.3:c.418A>G NP_002486.1:p.Lys140Glu
NR_134473.1:n.620A>G
NR_134474.1:n.537A>G
NR_134475.1:n.572A>G
NM_002495.4:c.418A>G MANE Select NP_002486.1:p.Lys140Glu
NM_001318051.2:c.350+12213A>G NP_001304980.1:n.350+12213A>G
NR_134473.2:n.614A>G
NR_134474.2:n.531A>G
NR_134475.2:n.566A>G