Canonical Allele Identifier: CA1969462144
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582327T= , CM000673.2:g.47582327T= GRCh38
NC_000011.9:g.47603879T= , CM000673.1:g.47603879T= GRCh37
NC_000011.8:g.47560455T= NCBI36
NG_011946.1:g.8318T=
NG_011946.2:g.8318T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.508-22T= MANE Select ENSP00000263774.4:n.508-22T=
ENST00000531351.2:n.1681T=
ENST00000677462.1:n.2982-22T=
ENST00000678975.1:n.2765-22T=
ENST00000263774.8:c.508-22T= ENSP00000263774.4:n.508-22T=
ENST00000524568.1:n.611-22T=
ENST00000525212.1:n.163-22T=
ENST00000525378.5:n.446-22T=
ENST00000527178.1:n.86T=
ENST00000533507.5:n.1402-22T=
NM_004551.2:c.508-22T= NP_004542.1:n.508-22T=
NM_004551.3:c.508-22T= MANE Select NP_004542.1:n.508-22T=