Canonical Allele Identifier: CA1980192857
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611977G= , CM000673.2:g.67611977G= GRCh38
NC_000011.9:g.67379448G= , CM000673.1:g.67379448G= GRCh37
NC_000011.8:g.67136024G= NCBI36
NG_013353.1:g.10126G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1161G= MANE Select ENSP00000322450.6:p.Glu387=
ENST00000647561.1:c.1161G= ENSP00000497587.1:p.Glu387=
ENST00000322776.10:c.1161G= ENSP00000322450.6:p.Glu387=
ENST00000415352.6:c.1140G= ENSP00000395368.2:p.Glu380=
ENST00000526770.5:n.1444G=
ENST00000527355.5:c.370-143G= ENSP00000432637.1:n.370-143G=
ENST00000527923.1:n.503G=
ENST00000529927.5:c.1134G= ENSP00000436766.1:p.Glu378=
ENST00000531250.1:n.425G=
ENST00000532303.5:c.858G= ENSP00000432015.1:p.Glu286=
ENST00000533919.5:c.565G= ENSP00000435199.1:n.565G=
ENST00000534352.1:n.259G=
NM_001166102.1:c.1134G= NP_001159574.1:p.Glu378=
NM_007103.3:c.1161G= NP_009034.2:p.Glu387=
NM_001166102.2:c.1134G= NP_001159574.1:p.Glu378=
NM_007103.4:c.1161G= MANE Select NP_009034.2:p.Glu387=