Canonical Allele Identifier: CA1969462117
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582282C= , CM000673.2:g.47582282C= GRCh38
NC_000011.9:g.47603834C= , CM000673.1:g.47603834C= GRCh37
NC_000011.8:g.47560410C= NCBI36
NG_011946.1:g.8273C=
NG_011946.2:g.8273C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-67C= MANE Select ENSP00000263774.4:n.508-67C=
ENST00000531351.2:n.1636C=
ENST00000677462.1:n.2982-67C=
ENST00000678975.1:n.2765-67C=
ENST00000263774.8:c.508-67C= ENSP00000263774.4:n.508-67C=
ENST00000524568.1:n.611-67C=
ENST00000525212.1:n.163-67C=
ENST00000525378.5:n.446-67C=
ENST00000527178.1:n.41C=
ENST00000533507.5:n.1402-67C=
NM_004551.2:c.508-67C= NP_004542.1:n.508-67C=
NM_004551.3:c.508-67C= MANE Select NP_004542.1:n.508-67C=