Canonical Allele Identifier: CA1980189908
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610457T= , CM000673.2:g.67610457T= GRCh38
NC_000011.9:g.67377928T= , CM000673.1:g.67377928T= GRCh37
NC_000011.8:g.67134504T= NCBI36
NG_013353.1:g.8606T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.587T= MANE Select ENSP00000322450.6:p.Phe196=
ENST00000647561.1:c.587T= ENSP00000497587.1:p.Phe196=
ENST00000322776.10:c.587T= ENSP00000322450.6:p.Phe196=
ENST00000415352.6:c.566T= ENSP00000395368.2:p.Phe189=
ENST00000526169.1:n.329T=
ENST00000526770.5:n.446T=
ENST00000529927.5:c.560T= ENSP00000436766.1:p.Phe187=
ENST00000532244.5:c.284T= ENSP00000435202.1:p.Phe95=
ENST00000532303.5:c.284T= ENSP00000432015.1:p.Phe95=
ENST00000532343.5:c.284T= ENSP00000431751.1:p.Phe95=
ENST00000533919.5:c.65T= ENSP00000435199.1:p.Phe22=
NM_001166102.1:c.560T= NP_001159574.1:p.Phe187=
NM_007103.3:c.587T= NP_009034.2:p.Phe196=
NM_001166102.2:c.560T= NP_001159574.1:p.Phe187=
NM_007103.4:c.587T= MANE Select NP_009034.2:p.Phe196=