Canonical Allele Identifier: CA475412839

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67610539-C-G
• MyVariant Identifiers: chr11:g.67378010C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610539C>G , CM000673.2:g.67610539C>G	GRCh38
NC_000011.9:g.67378010C>G , CM000673.1:g.67378010C>G	GRCh37
NC_000011.8:g.67134586C>G	NCBI36
NG_013353.1:g.8688C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.669C>G MANE Select	ENSP00000322450.6:p.Pro223=
ENST00000647561.1:c.669C>G	ENSP00000497587.1:p.Pro223=
ENST00000322776.10:c.669C>G	ENSP00000322450.6:p.Pro223=
ENST00000415352.6:c.648C>G	ENSP00000395368.2:p.Pro216=
ENST00000526169.1:n.411C>G
ENST00000526770.5:n.528C>G
ENST00000529927.5:c.642C>G	ENSP00000436766.1:p.Pro214=
ENST00000532244.5:c.366C>G	ENSP00000435202.1:p.Pro122=
ENST00000532303.5:c.366C>G	ENSP00000432015.1:p.Pro122=
ENST00000533919.5:c.147C>G	ENSP00000435199.1:p.Pro49=
NM_001166102.1:c.642C>G	NP_001159574.1:p.Pro214=
NM_007103.3:c.669C>G	NP_009034.2:p.Pro223=
NM_001166102.2:c.642C>G	NP_001159574.1:p.Pro214=
NM_007103.4:c.669C>G MANE Select	NP_009034.2:p.Pro223=