Canonical Allele Identifier: CA380361536

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47603902T>A (hg19) ; chr11:g.47582350T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582350T>A , CM000673.2:g.47582350T>A	GRCh38
NC_000011.9:g.47603902T>A , CM000673.1:g.47603902T>A	GRCh37
NC_000011.8:g.47560478T>A	NCBI36
NG_011946.1:g.8341T>A
NG_011946.2:g.8341T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.509T>A MANE Select	ENSP00000263774.4:p.Ile170Asn
ENST00000531351.2:n.1704T>A
ENST00000677462.1:n.2983T>A
ENST00000678975.1:n.2766T>A
ENST00000263774.8:c.509T>A	ENSP00000263774.4:p.Ile170Asn
ENST00000524568.1:n.612T>A
ENST00000525212.1:n.164T>A
ENST00000525378.5:n.447T>A
ENST00000527178.1:n.109T>A
ENST00000533507.5:n.1403T>A
NM_004551.2:c.509T>A	NP_004542.1:p.Ile170Asn
NM_004551.3:c.509T>A MANE Select	NP_004542.1:p.Ile170Asn