Canonical Allele Identifier: CA1980190067
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610522G= , CM000673.2:g.67610522G= GRCh38
NC_000011.9:g.67377993G= , CM000673.1:g.67377993G= GRCh37
NC_000011.8:g.67134569G= NCBI36
NG_013353.1:g.8671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.652G= MANE Select ENSP00000322450.6:p.Gly218=
ENST00000647561.1:c.652G= ENSP00000497587.1:p.Gly218=
ENST00000322776.10:c.652G= ENSP00000322450.6:p.Gly218=
ENST00000415352.6:c.631G= ENSP00000395368.2:p.Gly211=
ENST00000526169.1:n.394G=
ENST00000526770.5:n.511G=
ENST00000529927.5:c.625G= ENSP00000436766.1:p.Gly209=
ENST00000532244.5:c.349G= ENSP00000435202.1:p.Gly117=
ENST00000532303.5:c.349G= ENSP00000432015.1:p.Gly117=
ENST00000533919.5:c.130G= ENSP00000435199.1:p.Gly44=
NM_001166102.1:c.625G= NP_001159574.1:p.Gly209=
NM_007103.3:c.652G= NP_009034.2:p.Gly218=
NM_001166102.2:c.625G= NP_001159574.1:p.Gly209=
NM_007103.4:c.652G= MANE Select NP_009034.2:p.Gly218=