Canonical Allele Identifier: CA381536557

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67610411-C-A
• MyVariant Identifiers: chr11:g.67377882C>A (hg19) ; chr11:g.67610411C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67610411C>A , CM000673.2:g.67610411C>A	GRCh38
NC_000011.9:g.67377882C>A , CM000673.1:g.67377882C>A	GRCh37
NC_000011.8:g.67134458C>A	NCBI36
NG_013353.1:g.8560C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.541C>A MANE Select	ENSP00000322450.6:p.Leu181Met
ENST00000647561.1:c.541C>A	ENSP00000497587.1:p.Leu181Met
ENST00000322776.10:c.541C>A	ENSP00000322450.6:p.Leu181Met
ENST00000415352.6:c.520C>A	ENSP00000395368.2:p.Leu174Met
ENST00000526169.1:n.283C>A
ENST00000526770.5:n.400C>A
ENST00000529867.5:c.505C>A	ENSP00000434438.1:p.Leu169Met
ENST00000529927.5:c.514C>A	ENSP00000436766.1:p.Leu172Met
ENST00000530638.1:c.424C>A	ENSP00000436936.1:p.Leu142Met
ENST00000532244.5:c.238C>A	ENSP00000435202.1:p.Leu80Met
ENST00000532303.5:c.238C>A	ENSP00000432015.1:p.Leu80Met
ENST00000532343.5:c.238C>A	ENSP00000431751.1:p.Leu80Met
ENST00000533075.5:c.520C>A	ENSP00000437267.1:p.Leu174Met
ENST00000533919.5:c.19C>A	ENSP00000435199.1:p.Leu7Met
NM_001166102.1:c.514C>A	NP_001159574.1:p.Leu172Met
NM_007103.3:c.541C>A	NP_009034.2:p.Leu181Met
NM_001166102.2:c.514C>A	NP_001159574.1:p.Leu172Met
NM_007103.4:c.541C>A MANE Select	NP_009034.2:p.Leu181Met