Canonical Allele Identifier: CA359719614
Gene: NDUFS4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53646272A>G , CM000667.2:g.53646272A>G GRCh38
NC_000005.9:g.52942102A>G , CM000667.1:g.52942102A>G GRCh37
NC_000005.8:g.52977859A>G NCBI36
NG_008200.1:g.90638A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.217A>G MANE Select ENSP00000296684.5:p.Lys73Glu
ENST00000296684.9:c.217A>G ENSP00000296684.5:p.Lys73Glu
ENST00000502423.5:c.*84A>G ENSP00000422177.1:n.*84A>G
ENST00000506765.1:c.205A>G ENSP00000424570.1:p.Lys69Glu
ENST00000506974.5:c.389A>G ENSP00000425967.1:p.Lys130Arg
ENST00000507026.5:c.*191A>G ENSP00000424993.1:n.*191A>G
ENST00000509443.1:n.78A>G
NM_002495.2:c.217A>G NP_002486.1:p.Lys73Glu
XM_005248525.3:c.217A>G XP_005248582.1:p.Lys73Glu
XM_011543415.1:c.43A>G XP_011541717.1:p.Lys15Glu
NM_001318051.1:c.217A>G NP_001304980.1:p.Lys73Glu
NM_002495.3:c.217A>G NP_002486.1:p.Lys73Glu
NR_134473.1:n.419A>G
NR_134474.1:n.336A>G
NR_134475.1:n.371A>G
NM_002495.4:c.217A>G MANE Select NP_002486.1:p.Lys73Glu
NM_001318051.2:c.217A>G NP_001304980.1:p.Lys73Glu
NR_134473.2:n.413A>G
NR_134474.2:n.330A>G
NR_134475.2:n.365A>G