Canonical Allele Identifier: CA2613426625

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582324-CTGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582327_47582330del , CM000673.2:g.47582327_47582330del	GRCh38
NC_000011.9:g.47603879_47603882del , CM000673.1:g.47603879_47603882del	GRCh37
NC_000011.8:g.47560455_47560458del	NCBI36
NG_011946.1:g.8318_8321del
NG_011946.2:g.8318_8321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.508-22_508-19del MANE Select	ENSP00000263774.4:n.508-22_508-19del
ENST00000531351.2:n.1681_1684del
ENST00000677462.1:n.2982-22_2982-19del
ENST00000678975.1:n.2765-22_2765-19del
ENST00000263774.8:c.508-22_508-19del	ENSP00000263774.4:n.508-22_508-19del
ENST00000524568.1:n.611-22_611-19del
ENST00000525212.1:n.163-22_163-19del
ENST00000525378.5:n.446-22_446-19del
ENST00000527178.1:n.86_89del
ENST00000533507.5:n.1402-22_1402-19del
NM_004551.2:c.508-22_508-19del	NP_004542.1:n.508-22_508-19del
NM_004551.3:c.508-22_508-19del MANE Select	NP_004542.1:n.508-22_508-19del