Canonical Allele Identifier: CA2527766089
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610234dup , CM000673.2:g.67610234dup GRCh38
NC_000011.9:g.67377705dup , CM000673.1:g.67377705dup GRCh37
NC_000011.8:g.67134281dup NCBI36
NG_013353.1:g.8383dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.511-147dup MANE Select ENSP00000322450.6:n.511-147dup
ENST00000647561.1:c.511-147dup ENSP00000497587.1:n.511-147dup
ENST00000322776.10:c.511-147dup ENSP00000322450.6:n.511-147dup
ENST00000415352.6:c.490-147dup ENSP00000395368.2:n.490-147dup
ENST00000524838.5:n.1166dup
ENST00000526169.1:n.253-147dup
ENST00000526770.5:n.370-147dup
ENST00000529867.5:c.475-147dup ENSP00000434438.1:n.475-147dup
ENST00000529927.5:c.484-147dup ENSP00000436766.1:n.484-147dup
ENST00000530638.1:c.394-147dup ENSP00000436936.1:n.394-147dup
ENST00000532244.5:c.208-147dup ENSP00000435202.1:n.208-147dup
ENST00000532303.5:c.208-147dup ENSP00000432015.1:n.208-147dup
ENST00000532343.5:c.208-147dup ENSP00000431751.1:n.208-147dup
ENST00000533075.5:c.490-147dup ENSP00000437267.1:n.490-147dup
NM_001166102.1:c.484-147dup NP_001159574.1:n.484-147dup
NM_007103.3:c.511-147dup NP_009034.2:n.511-147dup
NM_001166102.2:c.484-147dup NP_001159574.1:n.484-147dup
NM_007103.4:c.511-147dup MANE Select NP_009034.2:n.511-147dup