Canonical Allele Identifier: CA2614647327
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610278G>T , CM000673.2:g.67610278G>T GRCh38
NC_000011.9:g.67377749G>T , CM000673.1:g.67377749G>T GRCh37
NC_000011.8:g.67134325G>T NCBI36
NG_013353.1:g.8427G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.511-103G>T MANE Select ENSP00000322450.6:n.511-103G>T
ENST00000647561.1:c.511-103G>T ENSP00000497587.1:n.511-103G>T
ENST00000322776.10:c.511-103G>T ENSP00000322450.6:n.511-103G>T
ENST00000415352.6:c.490-103G>T ENSP00000395368.2:n.490-103G>T
ENST00000526169.1:n.253-103G>T
ENST00000526770.5:n.370-103G>T
ENST00000529867.5:c.475-103G>T ENSP00000434438.1:n.475-103G>T
ENST00000529927.5:c.484-103G>T ENSP00000436766.1:n.484-103G>T
ENST00000530638.1:c.394-103G>T ENSP00000436936.1:n.394-103G>T
ENST00000532244.5:c.208-103G>T ENSP00000435202.1:n.208-103G>T
ENST00000532303.5:c.208-103G>T ENSP00000432015.1:n.208-103G>T
ENST00000532343.5:c.208-103G>T ENSP00000431751.1:n.208-103G>T
ENST00000533075.5:c.490-103G>T ENSP00000437267.1:n.490-103G>T
NM_001166102.1:c.484-103G>T NP_001159574.1:n.484-103G>T
NM_007103.3:c.511-103G>T NP_009034.2:n.511-103G>T
NM_001166102.2:c.484-103G>T NP_001159574.1:n.484-103G>T
NM_007103.4:c.511-103G>T MANE Select NP_009034.2:n.511-103G>T