Canonical Allele Identifier: CA381540898

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67611500-G-A
• MyVariant Identifiers: chr11:g.67378971G>A (hg19) ; chr11:g.67611500G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611500G>A , CM000673.2:g.67611500G>A	GRCh38
NC_000011.9:g.67378971G>A , CM000673.1:g.67378971G>A	GRCh37
NC_000011.8:g.67135547G>A	NCBI36
NG_013353.1:g.9649G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1011G>A MANE Select	ENSP00000322450.6:p.Met337Ile
ENST00000647561.1:c.1011G>A	ENSP00000497587.1:p.Met337Ile
ENST00000322776.10:c.1011G>A	ENSP00000322450.6:p.Met337Ile
ENST00000415352.6:c.990G>A	ENSP00000395368.2:p.Met330Ile
ENST00000526169.1:n.656-22G>A
ENST00000526770.5:n.1294G>A
ENST00000527355.5:c.300G>A	ENSP00000432637.1:p.Met100Ile
ENST00000527923.1:n.353G>A
ENST00000529927.5:c.984G>A	ENSP00000436766.1:p.Met328Ile
ENST00000532303.5:c.708G>A	ENSP00000432015.1:p.Met236Ile
ENST00000533919.5:c.415G>A	ENSP00000435199.1:n.415G>A
NM_001166102.1:c.984G>A	NP_001159574.1:p.Met328Ile
NM_007103.3:c.1011G>A	NP_009034.2:p.Met337Ile
NM_001166102.2:c.984G>A	NP_001159574.1:p.Met328Ile
NM_007103.4:c.1011G>A MANE Select	NP_009034.2:p.Met337Ile