Canonical Allele Identifier: CA381540868

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67611493-T-A
• MyVariant Identifiers: chr11:g.67378964T>A (hg19) ; chr11:g.67611493T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67611493T>A , CM000673.2:g.67611493T>A	GRCh38
NC_000011.9:g.67378964T>A , CM000673.1:g.67378964T>A	GRCh37
NC_000011.8:g.67135540T>A	NCBI36
NG_013353.1:g.9642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.1004T>A MANE Select	ENSP00000322450.6:p.Val335Glu
ENST00000647561.1:c.1004T>A	ENSP00000497587.1:p.Val335Glu
ENST00000322776.10:c.1004T>A	ENSP00000322450.6:p.Val335Glu
ENST00000415352.6:c.983T>A	ENSP00000395368.2:p.Val328Glu
ENST00000526169.1:n.656-29T>A
ENST00000526770.5:n.1287T>A
ENST00000527355.5:c.293T>A	ENSP00000432637.1:p.Val98Glu
ENST00000527923.1:n.346T>A
ENST00000529927.5:c.977T>A	ENSP00000436766.1:p.Val326Glu
ENST00000532303.5:c.701T>A	ENSP00000432015.1:p.Val234Glu
ENST00000533919.5:c.408T>A	ENSP00000435199.1:n.408T>A
NM_001166102.1:c.977T>A	NP_001159574.1:p.Val326Glu
NM_007103.3:c.1004T>A	NP_009034.2:p.Val335Glu
NM_001166102.2:c.977T>A	NP_001159574.1:p.Val326Glu
NM_007103.4:c.1004T>A MANE Select	NP_009034.2:p.Val335Glu