Canonical Allele Identifier: CA2724176158

Gene: NDUFS3

Linked Data

• dbSNP Id: rs2153795407

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582473_47582474insGTGGTGGC , CM000673.2:g.47582473_47582474insGTGGTGGC	GRCh38
NC_000011.9:g.47604025_47604026insGTGGTGGC , CM000673.1:g.47604025_47604026insGTGGTGGC	GRCh37
NC_000011.8:g.47560601_47560602insGTGGTGGC	NCBI36
NG_011946.1:g.8464_8465insGTGGTGGC
NG_011946.2:g.8464_8465insGTGGTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+5_627+6insGTGGTGGC MANE Select	ENSP00000263774.4:n.627+5_627+6insGTGGTGGC
ENST00000531351.2:n.1822+5_1822+6insGTGGTGGC
ENST00000677462.1:n.3101+5_3101+6insGTGGTGGC
ENST00000678975.1:n.2884+5_2884+6insGTGGTGGC
ENST00000263774.8:c.627+5_627+6insGTGGTGGC	ENSP00000263774.4:n.627+5_627+6insGTGGTGGC
ENST00000525212.1:n.282+5_282+6insGTGGTGGC
ENST00000525378.5:n.565+5_565+6insGTGGTGGC
ENST00000527178.1:n.227+5_227+6insGTGGTGGC
ENST00000533507.5:n.1521+5_1521+6insGTGGTGGC
NM_004551.2:c.627+5_627+6insGTGGTGGC	NP_004542.1:n.627+5_627+6insGTGGTGGC
NM_004551.3:c.627+5_627+6insGTGGTGGC MANE Select	NP_004542.1:n.627+5_627+6insGTGGTGGC