Canonical Allele Identifier: CA1980191832
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611463C= , CM000673.2:g.67611463C= GRCh38
NC_000011.9:g.67378934C= , CM000673.1:g.67378934C= GRCh37
NC_000011.8:g.67135510C= NCBI36
NG_013353.1:g.9612C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.974C= MANE Select ENSP00000322450.6:p.Pro325=
ENST00000647561.1:c.974C= ENSP00000497587.1:p.Pro325=
ENST00000322776.10:c.974C= ENSP00000322450.6:p.Pro325=
ENST00000415352.6:c.953C= ENSP00000395368.2:p.Pro318=
ENST00000526169.1:n.656-59C=
ENST00000526770.5:n.1257C=
ENST00000527355.5:c.263C= ENSP00000432637.1:p.Pro88=
ENST00000527923.1:n.316C=
ENST00000529927.5:c.947C= ENSP00000436766.1:p.Pro316=
ENST00000532303.5:c.671C= ENSP00000432015.1:p.Pro224=
ENST00000533919.5:c.392-14C= ENSP00000435199.1:n.392-14C=
NM_001166102.1:c.947C= NP_001159574.1:p.Pro316=
NM_007103.3:c.974C= NP_009034.2:p.Pro325=
NM_001166102.2:c.947C= NP_001159574.1:p.Pro316=
NM_007103.4:c.974C= MANE Select NP_009034.2:p.Pro325=