Canonical Allele Identifier: CA1546620655
Gene: NDUFS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560636T= , CM000667.2:g.53560636T= GRCh38
NC_000005.9:g.52856466T= , CM000667.1:g.52856466T= GRCh37
NC_000005.8:g.52892223T= NCBI36
NG_008200.1:g.5002T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296684.9:c.-27T= ENSP00000296684.5:n.-27T=
ENST00000502423.5:c.-27T= ENSP00000422177.1:n.-27T=
ENST00000507026.5:c.-27T= ENSP00000424993.1:n.-27T=
NM_002495.2:c.-27T= NP_002486.1:n.-27T=
XM_005248525.3:c.-27T= XP_005248582.1:n.-27T=
XM_011543414.1:c.-27T= XP_011541716.1:n.-27T=
NM_001318051.1:c.-27T= NP_001304980.1:n.-27T=
NM_002495.3:c.-27T= NP_002486.1:n.-27T=
NR_134473.1:n.4T=
NR_134474.1:n.4T=
NR_134475.1:n.4T=
XM_017009491.1:c.-27T= XP_016864980.1:n.-27T=