Canonical Allele Identifier: CA2673829523
Gene: NDUFS4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53658783_53658784insAAAAA , CM000667.2:g.53658783_53658784insAAAAA GRCh38
NC_000005.9:g.52954613_52954614insAAAAA , CM000667.1:g.52954613_52954614insAAAAA GRCh37
NC_000005.8:g.52990370_52990371insAAAAA NCBI36
NG_008200.1:g.103149_103150insAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.424+159_424+160insAAAAA MANE Select ENSP00000296684.5:n.424+159_424+160insAAAAA
ENST00000296684.9:c.424+159_424+160insAAAAA ENSP00000296684.5:n.424+159_424+160insAAAAA
ENST00000502423.5:c.*291+159_*291+160insAAAAA ENSP00000422177.1:n.*291+159_*291+160insAAAAA
ENST00000506765.1:c.338+12378_338+12379insAAAAA ENSP00000424570.1:n.338+12378_338+12379insAAAAA
ENST00000506974.5:c.*200+159_*200+160insAAAAA ENSP00000425967.1:n.*200+159_*200+160insAAAAA
ENST00000507026.5:c.*398+159_*398+160insAAAAA ENSP00000424993.1:n.*398+159_*398+160insAAAAA
ENST00000509443.1:n.444_445insAAAAA
NM_002495.2:c.424+159_424+160insAAAAA NP_002486.1:n.424+159_424+160insAAAAA
XM_005248525.3:c.350+12378_350+12379insAAAAA XP_005248582.1:n.350+12378_350+12379insAAAAA
XM_011543415.1:c.250+159_250+160insAAAAA XP_011541717.1:n.250+159_250+160insAAAAA
NM_001318051.1:c.350+12378_350+12379insAAAAA NP_001304980.1:n.350+12378_350+12379insAAAAA
NM_002495.3:c.424+159_424+160insAAAAA NP_002486.1:n.424+159_424+160insAAAAA
NR_134473.1:n.626+159_626+160insAAAAA
NR_134474.1:n.543+159_543+160insAAAAA
NR_134475.1:n.578+159_578+160insAAAAA
NM_002495.4:c.424+159_424+160insAAAAA MANE Select NP_002486.1:n.424+159_424+160insAAAAA
NM_001318051.2:c.350+12378_350+12379insAAAAA NP_001304980.1:n.350+12378_350+12379insAAAAA
NR_134473.2:n.620+159_620+160insAAAAA
NR_134474.2:n.537+159_537+160insAAAAA
NR_134475.2:n.572+159_572+160insAAAAA