Canonical Allele Identifier: CA1969462262
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582625_47582627delinsCAA , CM000673.2:g.47582625_47582627delinsCAA GRCh38
NC_000011.9:g.47604177_47604179delinsCAA , CM000673.1:g.47604177_47604179delinsCAA GRCh37
NC_000011.8:g.47560753_47560755delinsCAA NCBI36
NG_011946.1:g.8616_8618delinsCAA
NG_011946.2:g.8616_8618delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+157_627+159delinsCAA MANE Select ENSP00000263774.4:n.627+157_627+159delinsCAA
ENST00000531351.2:n.1822+157_1822+159delinsCAA
ENST00000677462.1:n.3101+157_3101+159delinsCAA
ENST00000678975.1:n.2884+157_2884+159delinsCAA
ENST00000263774.8:c.627+157_627+159delinsCAA ENSP00000263774.4:n.627+157_627+159delinsCAA
ENST00000525212.1:n.282+157_282+159delinsCAA
ENST00000525378.5:n.565+157_565+159delinsCAA
ENST00000527178.1:n.227+157_227+159delinsCAA
ENST00000533507.5:n.1521+157_1521+159delinsCAA
NM_004551.2:c.627+157_627+159delinsCAA NP_004542.1:n.627+157_627+159delinsCAA
NM_004551.3:c.627+157_627+159delinsCAA MANE Select NP_004542.1:n.627+157_627+159delinsCAA