Canonical Allele Identifier: CA381535210
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67609477G>T , CM000673.2:g.67609477G>T GRCh38
NC_000011.9:g.67376948G>T , CM000673.1:g.67376948G>T GRCh37
NC_000011.8:g.67133524G>T NCBI36
NG_013353.1:g.7626G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.352G>T MANE Select ENSP00000322450.6:p.Asp118Tyr
ENST00000647561.1:c.352G>T ENSP00000497587.1:p.Asp118Tyr
ENST00000322776.10:c.352G>T ENSP00000322450.6:p.Asp118Tyr
ENST00000415352.6:c.331G>T ENSP00000395368.2:p.Asp111Tyr
ENST00000524838.5:n.409G>T
ENST00000525086.5:n.425G>T
ENST00000526169.1:n.94G>T
ENST00000526770.5:n.211G>T
ENST00000528314.1:c.49G>T ENSP00000434581.1:p.Asp17Tyr
ENST00000528377.1:n.523G>T
ENST00000529867.5:c.316G>T ENSP00000434438.1:p.Asp106Tyr
ENST00000529927.5:c.325G>T ENSP00000436766.1:p.Asp109Tyr
ENST00000530014.5:n.647G>T
ENST00000530103.5:c.*246G>T ENSP00000434575.1:n.*246G>T
ENST00000530638.1:c.235G>T ENSP00000436936.1:p.Asp79Tyr
ENST00000532244.5:c.49G>T ENSP00000435202.1:p.Asp17Tyr
ENST00000532303.5:c.49G>T ENSP00000432015.1:p.Asp17Tyr
ENST00000532343.5:c.49G>T ENSP00000431751.1:p.Asp17Tyr
ENST00000533075.5:c.331G>T ENSP00000437267.1:p.Asp111Tyr
ENST00000534139.5:n.468G>T
NM_001166102.1:c.325G>T NP_001159574.1:p.Asp109Tyr
NM_007103.3:c.352G>T NP_009034.2:p.Asp118Tyr
NM_001166102.2:c.325G>T NP_001159574.1:p.Asp109Tyr
NM_007103.4:c.352G>T MANE Select NP_009034.2:p.Asp118Tyr