Canonical Allele Identifier: CA1980188270
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67609480G= , CM000673.2:g.67609480G= GRCh38
NC_000011.9:g.67376951G= , CM000673.1:g.67376951G= GRCh37
NC_000011.8:g.67133527G= NCBI36
NG_013353.1:g.7629G=

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.355G= MANE Select ENSP00000322450.6:p.Glu119=
ENST00000647561.1:c.355G= ENSP00000497587.1:p.Glu119=
ENST00000322776.10:c.355G= ENSP00000322450.6:p.Glu119=
ENST00000415352.6:c.334G= ENSP00000395368.2:p.Glu112=
ENST00000524838.5:n.412G=
ENST00000525086.5:n.428G=
ENST00000526169.1:n.97G=
ENST00000526770.5:n.214G=
ENST00000528314.1:c.52G= ENSP00000434581.1:p.Glu18=
ENST00000528377.1:n.526G=
ENST00000529867.5:c.319G= ENSP00000434438.1:p.Glu107=
ENST00000529927.5:c.328G= ENSP00000436766.1:p.Glu110=
ENST00000530014.5:n.650G=
ENST00000530103.5:c.*249G= ENSP00000434575.1:n.*249G=
ENST00000530638.1:c.238G= ENSP00000436936.1:p.Glu80=
ENST00000532244.5:c.52G= ENSP00000435202.1:p.Glu18=
ENST00000532303.5:c.52G= ENSP00000432015.1:p.Glu18=
ENST00000532343.5:c.52G= ENSP00000431751.1:p.Glu18=
ENST00000533075.5:c.334G= ENSP00000437267.1:p.Glu112=
ENST00000534139.5:n.471G=
NM_001166102.1:c.328G= NP_001159574.1:p.Glu110=
NM_007103.3:c.355G= NP_009034.2:p.Glu119=
NM_001166102.2:c.328G= NP_001159574.1:p.Glu110=
NM_007103.4:c.355G= MANE Select NP_009034.2:p.Glu119=