Canonical Allele Identifier: CA381536412

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377858A>G (hg19) ; chr11:g.67610387A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610387A>G , CM000673.2:g.67610387A>G	GRCh38
NC_000011.9:g.67377858A>G , CM000673.1:g.67377858A>G	GRCh37
NC_000011.8:g.67134434A>G	NCBI36
NG_013353.1:g.8536A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.517A>G MANE Select	ENSP00000322450.6:p.Ile173Val
ENST00000647561.1:c.517A>G	ENSP00000497587.1:p.Ile173Val
ENST00000322776.10:c.517A>G	ENSP00000322450.6:p.Ile173Val
ENST00000415352.6:c.496A>G	ENSP00000395368.2:p.Ile166Val
ENST00000526169.1:n.259A>G
ENST00000526770.5:n.376A>G
ENST00000529867.5:c.481A>G	ENSP00000434438.1:p.Ile161Val
ENST00000529927.5:c.490A>G	ENSP00000436766.1:p.Ile164Val
ENST00000530638.1:c.400A>G	ENSP00000436936.1:p.Ile134Val
ENST00000532244.5:c.214A>G	ENSP00000435202.1:p.Ile72Val
ENST00000532303.5:c.214A>G	ENSP00000432015.1:p.Ile72Val
ENST00000532343.5:c.214A>G	ENSP00000431751.1:p.Ile72Val
ENST00000533075.5:c.496A>G	ENSP00000437267.1:p.Ile166Val
NM_001166102.1:c.490A>G	NP_001159574.1:p.Ile164Val
NM_007103.3:c.517A>G	NP_009034.2:p.Ile173Val
NM_001166102.2:c.490A>G	NP_001159574.1:p.Ile164Val
NM_007103.4:c.517A>G MANE Select	NP_009034.2:p.Ile173Val