Canonical Allele Identifier: CA380362026

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47603999T>A (hg19) ; chr11:g.47582447T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582447T>A , CM000673.2:g.47582447T>A	GRCh38
NC_000011.9:g.47603999T>A , CM000673.1:g.47603999T>A	GRCh37
NC_000011.8:g.47560575T>A	NCBI36
NG_011946.1:g.8438T>A
NG_011946.2:g.8438T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.606T>A MANE Select	ENSP00000263774.4:p.Phe202Leu
ENST00000531351.2:n.1801T>A
ENST00000677462.1:n.3080T>A
ENST00000678975.1:n.2863T>A
ENST00000263774.8:c.606T>A	ENSP00000263774.4:p.Phe202Leu
ENST00000524568.1:n.709T>A
ENST00000525212.1:n.261T>A
ENST00000525378.5:n.544T>A
ENST00000527178.1:n.206T>A
ENST00000533507.5:n.1500T>A
NM_004551.2:c.606T>A	NP_004542.1:p.Phe202Leu
NM_004551.3:c.606T>A MANE Select	NP_004542.1:p.Phe202Leu