Canonical Allele Identifier: CA2673829548
Gene: NDUFS4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53658797_53658798insGA , CM000667.2:g.53658797_53658798insGA GRCh38
NC_000005.9:g.52954627_52954628insGA , CM000667.1:g.52954627_52954628insGA GRCh37
NC_000005.8:g.52990384_52990385insGA NCBI36
NG_008200.1:g.103163_103164insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.10:c.424+173_424+174insGA MANE Select ENSP00000296684.5:n.424+173_424+174insGA
ENST00000296684.9:c.424+173_424+174insGA ENSP00000296684.5:n.424+173_424+174insGA
ENST00000502423.5:c.*291+173_*291+174insGA ENSP00000422177.1:n.*291+173_*291+174insGA
ENST00000506765.1:c.338+12392_338+12393insGA ENSP00000424570.1:n.338+12392_338+12393insGA
ENST00000506974.5:c.*200+173_*200+174insGA ENSP00000425967.1:n.*200+173_*200+174insGA
ENST00000507026.5:c.*398+173_*398+174insGA ENSP00000424993.1:n.*398+173_*398+174insGA
NM_002495.2:c.424+173_424+174insGA NP_002486.1:n.424+173_424+174insGA
XM_005248525.3:c.350+12392_350+12393insGA XP_005248582.1:n.350+12392_350+12393insGA
XM_011543415.1:c.250+173_250+174insGA XP_011541717.1:n.250+173_250+174insGA
NM_001318051.1:c.350+12392_350+12393insGA NP_001304980.1:n.350+12392_350+12393insGA
NM_002495.3:c.424+173_424+174insGA NP_002486.1:n.424+173_424+174insGA
NR_134473.1:n.626+173_626+174insGA
NR_134474.1:n.543+173_543+174insGA
NR_134475.1:n.578+173_578+174insGA
NM_002495.4:c.424+173_424+174insGA MANE Select NP_002486.1:n.424+173_424+174insGA
NM_001318051.2:c.350+12392_350+12393insGA NP_001304980.1:n.350+12392_350+12393insGA
NR_134473.2:n.620+173_620+174insGA
NR_134474.2:n.537+173_537+174insGA
NR_134475.2:n.572+173_572+174insGA