Canonical Allele Identifier: CA381536658
Gene: NDUFV1 HGNC NCBI

Linked Data

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