Canonical Allele Identifier: CA475417459

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67611515-G-A
• MyVariant Identifiers: chr11:g.67378986G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611515G>A , CM000673.2:g.67611515G>A	GRCh38
NC_000011.9:g.67378986G>A , CM000673.1:g.67378986G>A	GRCh37
NC_000011.8:g.67135562G>A	NCBI36
NG_013353.1:g.9664G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000322776.11:c.1026G>A MANE Select	ENSP00000322450.6:p.Leu342=
ENST00000647561.1:c.1026G>A	ENSP00000497587.1:p.Leu342=
ENST00000322776.10:c.1026G>A	ENSP00000322450.6:p.Leu342=
ENST00000415352.6:c.1005G>A	ENSP00000395368.2:p.Leu335=
ENST00000526169.1:n.656-7G>A
ENST00000526770.5:n.1309G>A
ENST00000527355.5:c.315G>A	ENSP00000432637.1:p.Leu105=
ENST00000527923.1:n.368G>A
ENST00000529927.5:c.999G>A	ENSP00000436766.1:p.Leu333=
ENST00000532303.5:c.723G>A	ENSP00000432015.1:p.Leu241=
ENST00000533919.5:c.430G>A	ENSP00000435199.1:n.430G>A
NM_001166102.1:c.999G>A	NP_001159574.1:p.Leu333=
NM_007103.3:c.1026G>A	NP_009034.2:p.Leu342=
NM_001166102.2:c.999G>A	NP_001159574.1:p.Leu333=
NM_007103.4:c.1026G>A MANE Select	NP_009034.2:p.Leu342=