Canonical Allele Identifier: CA381536598

Gene: NDUFV1

Linked Data

• MyVariant Identifiers: chr11:g.67377889G>A (hg19) ; chr11:g.67610418G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610418G>A , CM000673.2:g.67610418G>A	GRCh38
NC_000011.9:g.67377889G>A , CM000673.1:g.67377889G>A	GRCh37
NC_000011.8:g.67134465G>A	NCBI36
NG_013353.1:g.8567G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.548G>A MANE Select	ENSP00000322450.6:p.Gly183Asp
ENST00000647561.1:c.548G>A	ENSP00000497587.1:p.Gly183Asp
ENST00000322776.10:c.548G>A	ENSP00000322450.6:p.Gly183Asp
ENST00000415352.6:c.527G>A	ENSP00000395368.2:p.Gly176Asp
ENST00000526169.1:n.290G>A
ENST00000526770.5:n.407G>A
ENST00000529867.5:c.512G>A	ENSP00000434438.1:p.Gly171Asp
ENST00000529927.5:c.521G>A	ENSP00000436766.1:p.Gly174Asp
ENST00000530638.1:c.431G>A	ENSP00000436936.1:p.Gly144Asp
ENST00000532244.5:c.245G>A	ENSP00000435202.1:p.Gly82Asp
ENST00000532303.5:c.245G>A	ENSP00000432015.1:p.Gly82Asp
ENST00000532343.5:c.245G>A	ENSP00000431751.1:p.Gly82Asp
ENST00000533075.5:c.527G>A	ENSP00000437267.1:p.Gly176Asp
ENST00000533919.5:c.26G>A	ENSP00000435199.1:p.Gly9Asp
NM_001166102.1:c.521G>A	NP_001159574.1:p.Gly174Asp
NM_007103.3:c.548G>A	NP_009034.2:p.Gly183Asp
NM_001166102.2:c.521G>A	NP_001159574.1:p.Gly174Asp
NM_007103.4:c.548G>A MANE Select	NP_009034.2:p.Gly183Asp