Canonical Allele Identifier: CA381535218

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67376949A>G (hg19) ; chr11:g.67609478A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67609478A>G , CM000673.2:g.67609478A>G	GRCh38
NC_000011.9:g.67376949A>G , CM000673.1:g.67376949A>G	GRCh37
NC_000011.8:g.67133525A>G	NCBI36
NG_013353.1:g.7627A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.353A>G MANE Select	ENSP00000322450.6:p.Asp118Gly
ENST00000647561.1:c.353A>G	ENSP00000497587.1:p.Asp118Gly
ENST00000322776.10:c.353A>G	ENSP00000322450.6:p.Asp118Gly
ENST00000415352.6:c.332A>G	ENSP00000395368.2:p.Asp111Gly
ENST00000524838.5:n.410A>G
ENST00000525086.5:n.426A>G
ENST00000526169.1:n.95A>G
ENST00000526770.5:n.212A>G
ENST00000528314.1:c.50A>G	ENSP00000434581.1:p.Asp17Gly
ENST00000528377.1:n.524A>G
ENST00000529867.5:c.317A>G	ENSP00000434438.1:p.Asp106Gly
ENST00000529927.5:c.326A>G	ENSP00000436766.1:p.Asp109Gly
ENST00000530014.5:n.648A>G
ENST00000530103.5:c.*247A>G	ENSP00000434575.1:n.*247A>G
ENST00000530638.1:c.236A>G	ENSP00000436936.1:p.Asp79Gly
ENST00000532244.5:c.50A>G	ENSP00000435202.1:p.Asp17Gly
ENST00000532303.5:c.50A>G	ENSP00000432015.1:p.Asp17Gly
ENST00000532343.5:c.50A>G	ENSP00000431751.1:p.Asp17Gly
ENST00000533075.5:c.332A>G	ENSP00000437267.1:p.Asp111Gly
ENST00000534139.5:n.469A>G
NM_001166102.1:c.326A>G	NP_001159574.1:p.Asp109Gly
NM_007103.3:c.353A>G	NP_009034.2:p.Asp118Gly
NM_001166102.2:c.326A>G	NP_001159574.1:p.Asp109Gly
NM_007103.4:c.353A>G MANE Select	NP_009034.2:p.Asp118Gly