Canonical Allele Identifier: CA2614647344
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610296C>G , CM000673.2:g.67610296C>G GRCh38
NC_000011.9:g.67377767C>G , CM000673.1:g.67377767C>G GRCh37
NC_000011.8:g.67134343C>G NCBI36
NG_013353.1:g.8445C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.511-85C>G MANE Select ENSP00000322450.6:n.511-85C>G
ENST00000647561.1:c.511-85C>G ENSP00000497587.1:n.511-85C>G
ENST00000322776.10:c.511-85C>G ENSP00000322450.6:n.511-85C>G
ENST00000415352.6:c.490-85C>G ENSP00000395368.2:n.490-85C>G
ENST00000526169.1:n.253-85C>G
ENST00000526770.5:n.370-85C>G
ENST00000529867.5:c.475-85C>G ENSP00000434438.1:n.475-85C>G
ENST00000529927.5:c.484-85C>G ENSP00000436766.1:n.484-85C>G
ENST00000530638.1:c.394-85C>G ENSP00000436936.1:n.394-85C>G
ENST00000532244.5:c.208-85C>G ENSP00000435202.1:n.208-85C>G
ENST00000532303.5:c.208-85C>G ENSP00000432015.1:n.208-85C>G
ENST00000532343.5:c.208-85C>G ENSP00000431751.1:n.208-85C>G
ENST00000533075.5:c.490-85C>G ENSP00000437267.1:n.490-85C>G
NM_001166102.1:c.484-85C>G NP_001159574.1:n.484-85C>G
NM_007103.3:c.511-85C>G NP_009034.2:n.511-85C>G
NM_001166102.2:c.484-85C>G NP_001159574.1:n.484-85C>G
NM_007103.4:c.511-85C>G MANE Select NP_009034.2:n.511-85C>G