Canonical Allele Identifier: CA381535271

Gene: NDUFV1

Linked Data

• gnomAD v4: 11-67609484-G-A
• MyVariant Identifiers: chr11:g.67376955G>A (hg19) ; chr11:g.67609484G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67609484G>A , CM000673.2:g.67609484G>A	GRCh38
NC_000011.9:g.67376955G>A , CM000673.1:g.67376955G>A	GRCh37
NC_000011.8:g.67133531G>A	NCBI36
NG_013353.1:g.7633G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322776.11:c.359G>A MANE Select	ENSP00000322450.6:p.Gly120Glu
ENST00000647561.1:c.359G>A	ENSP00000497587.1:p.Gly120Glu
ENST00000322776.10:c.359G>A	ENSP00000322450.6:p.Gly120Glu
ENST00000415352.6:c.338G>A	ENSP00000395368.2:p.Gly113Glu
ENST00000524838.5:n.416G>A
ENST00000525086.5:n.432G>A
ENST00000526169.1:n.101G>A
ENST00000526770.5:n.218G>A
ENST00000528314.1:c.56G>A	ENSP00000434581.1:p.Gly19Glu
ENST00000528377.1:n.530G>A
ENST00000529867.5:c.323G>A	ENSP00000434438.1:p.Gly108Glu
ENST00000529927.5:c.332G>A	ENSP00000436766.1:p.Gly111Glu
ENST00000530014.5:n.654G>A
ENST00000530103.5:c.*253G>A	ENSP00000434575.1:n.*253G>A
ENST00000530638.1:c.242G>A	ENSP00000436936.1:p.Gly81Glu
ENST00000532244.5:c.56G>A	ENSP00000435202.1:p.Gly19Glu
ENST00000532303.5:c.56G>A	ENSP00000432015.1:p.Gly19Glu
ENST00000532343.5:c.56G>A	ENSP00000431751.1:p.Gly19Glu
ENST00000533075.5:c.338G>A	ENSP00000437267.1:p.Gly113Glu
ENST00000534139.5:n.475G>A
NM_001166102.1:c.332G>A	NP_001159574.1:p.Gly111Glu
NM_007103.3:c.359G>A	NP_009034.2:p.Gly120Glu
NM_001166102.2:c.332G>A	NP_001159574.1:p.Gly111Glu
NM_007103.4:c.359G>A MANE Select	NP_009034.2:p.Gly120Glu