Canonical Allele Identifier: CA381536966

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377954A>G (hg19) ; chr11:g.67610483A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610483A>G , CM000673.2:g.67610483A>G	GRCh38
NC_000011.9:g.67377954A>G , CM000673.1:g.67377954A>G	GRCh37
NC_000011.8:g.67134530A>G	NCBI36
NG_013353.1:g.8632A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.613A>G MANE Select	ENSP00000322450.6:p.Ile205Val
ENST00000647561.1:c.613A>G	ENSP00000497587.1:p.Ile205Val
ENST00000322776.10:c.613A>G	ENSP00000322450.6:p.Ile205Val
ENST00000415352.6:c.592A>G	ENSP00000395368.2:p.Ile198Val
ENST00000526169.1:n.355A>G
ENST00000526770.5:n.472A>G
ENST00000529927.5:c.586A>G	ENSP00000436766.1:p.Ile196Val
ENST00000532244.5:c.310A>G	ENSP00000435202.1:p.Ile104Val
ENST00000532303.5:c.310A>G	ENSP00000432015.1:p.Ile104Val
ENST00000533919.5:c.91A>G	ENSP00000435199.1:p.Ile31Val
NM_001166102.1:c.586A>G	NP_001159574.1:p.Ile196Val
NM_007103.3:c.613A>G	NP_009034.2:p.Ile205Val
NM_001166102.2:c.586A>G	NP_001159574.1:p.Ile196Val
NM_007103.4:c.613A>G MANE Select	NP_009034.2:p.Ile205Val