Canonical Allele Identifier: CA1980192020
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611511C= , CM000673.2:g.67611511C= GRCh38
NC_000011.9:g.67378982C= , CM000673.1:g.67378982C= GRCh37
NC_000011.8:g.67135558C= NCBI36
NG_013353.1:g.9660C=

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1022C= MANE Select ENSP00000322450.6:p.Ala341=
ENST00000647561.1:c.1022C= ENSP00000497587.1:p.Ala341=
ENST00000322776.10:c.1022C= ENSP00000322450.6:p.Ala341=
ENST00000415352.6:c.1001C= ENSP00000395368.2:p.Ala334=
ENST00000526169.1:n.656-11C=
ENST00000526770.5:n.1305C=
ENST00000527355.5:c.311C= ENSP00000432637.1:p.Ala104=
ENST00000527923.1:n.364C=
ENST00000529927.5:c.995C= ENSP00000436766.1:p.Ala332=
ENST00000532303.5:c.719C= ENSP00000432015.1:p.Ala240=
ENST00000533919.5:c.426C= ENSP00000435199.1:n.426C=
NM_001166102.1:c.995C= NP_001159574.1:p.Ala332=
NM_007103.3:c.1022C= NP_009034.2:p.Ala341=
NM_001166102.2:c.995C= NP_001159574.1:p.Ala332=
NM_007103.4:c.1022C= MANE Select NP_009034.2:p.Ala341=