Canonical Allele Identifier: CA2613426872

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582529-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582531_47582532del , CM000673.2:g.47582531_47582532del	GRCh38
NC_000011.9:g.47604083_47604084del , CM000673.1:g.47604083_47604084del	GRCh37
NC_000011.8:g.47560659_47560660del	NCBI36
NG_011946.1:g.8522_8523del
NG_011946.2:g.8522_8523del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+63_627+64del MANE Select	ENSP00000263774.4:n.627+63_627+64del
ENST00000531351.2:n.1822+63_1822+64del
ENST00000677462.1:n.3101+63_3101+64del
ENST00000678975.1:n.2884+63_2884+64del
ENST00000263774.8:c.627+63_627+64del	ENSP00000263774.4:n.627+63_627+64del
ENST00000525212.1:n.282+63_282+64del
ENST00000525378.5:n.565+63_565+64del
ENST00000527178.1:n.227+63_227+64del
ENST00000533507.5:n.1521+63_1521+64del
NM_004551.2:c.627+63_627+64del	NP_004542.1:n.627+63_627+64del
NM_004551.3:c.627+63_627+64del MANE Select	NP_004542.1:n.627+63_627+64del