Canonical Allele Identifier: CA381536658

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67610426-G-A
• MyVariant Identifiers: chr11:g.67377897G>A (hg19) ; chr11:g.67610426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610426G>A , CM000673.2:g.67610426G>A	GRCh38
NC_000011.9:g.67377897G>A , CM000673.1:g.67377897G>A	GRCh37
NC_000011.8:g.67134473G>A	NCBI36
NG_013353.1:g.8575G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.556G>A MANE Select	ENSP00000322450.6:p.Ala186Thr
ENST00000647561.1:c.556G>A	ENSP00000497587.1:p.Ala186Thr
ENST00000322776.10:c.556G>A	ENSP00000322450.6:p.Ala186Thr
ENST00000415352.6:c.535G>A	ENSP00000395368.2:p.Ala179Thr
ENST00000526169.1:n.298G>A
ENST00000526770.5:n.415G>A
ENST00000529867.5:c.520G>A	ENSP00000434438.1:p.Ala174Thr
ENST00000529927.5:c.529G>A	ENSP00000436766.1:p.Ala177Thr
ENST00000532244.5:c.253G>A	ENSP00000435202.1:p.Ala85Thr
ENST00000532303.5:c.253G>A	ENSP00000432015.1:p.Ala85Thr
ENST00000532343.5:c.253G>A	ENSP00000431751.1:p.Ala85Thr
ENST00000533075.5:c.535G>A
ENST00000533919.5:c.34G>A	ENSP00000435199.1:p.Ala12Thr
NM_001166102.1:c.529G>A	NP_001159574.1:p.Ala177Thr
NM_007103.3:c.556G>A	NP_009034.2:p.Ala186Thr
NM_001166102.2:c.529G>A	NP_001159574.1:p.Ala177Thr
NM_007103.4:c.556G>A MANE Select	NP_009034.2:p.Ala186Thr