Canonical Allele Identifier: CA381536674

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67610427-C-G
• MyVariant Identifiers: chr11:g.67377898C>G (hg19) ; chr11:g.67610427C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610427C>G , CM000673.2:g.67610427C>G	GRCh38
NC_000011.9:g.67377898C>G , CM000673.1:g.67377898C>G	GRCh37
NC_000011.8:g.67134474C>G	NCBI36
NG_013353.1:g.8576C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.557C>G MANE Select	ENSP00000322450.6:p.Ala186Gly
ENST00000647561.1:c.557C>G	ENSP00000497587.1:p.Ala186Gly
ENST00000322776.10:c.557C>G	ENSP00000322450.6:p.Ala186Gly
ENST00000415352.6:c.536C>G	ENSP00000395368.2:p.Ala179Gly
ENST00000526169.1:n.299C>G
ENST00000526770.5:n.416C>G
ENST00000529867.5:c.521C>G	ENSP00000434438.1:p.Ala174Gly
ENST00000529927.5:c.530C>G	ENSP00000436766.1:p.Ala177Gly
ENST00000532244.5:c.254C>G	ENSP00000435202.1:p.Ala85Gly
ENST00000532303.5:c.254C>G	ENSP00000432015.1:p.Ala85Gly
ENST00000532343.5:c.254C>G	ENSP00000431751.1:p.Ala85Gly
ENST00000533919.5:c.35C>G	ENSP00000435199.1:p.Ala12Gly
NM_001166102.1:c.530C>G	NP_001159574.1:p.Ala177Gly
NM_007103.3:c.557C>G	NP_009034.2:p.Ala186Gly
NM_001166102.2:c.530C>G	NP_001159574.1:p.Ala177Gly
NM_007103.4:c.557C>G MANE Select	NP_009034.2:p.Ala186Gly