Canonical Allele Identifier: CA2695214864
Gene: NDUFV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2907412
ClinVar RCV Id: RCV003727120

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611395_67611436del , CM000673.2:g.67611395_67611436del GRCh38
NC_000011.9:g.67378866_67378907del , CM000673.1:g.67378866_67378907del GRCh37
NC_000011.8:g.67135442_67135483del NCBI36
NG_013353.1:g.9544_9585del

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.914-8_947del
ENST00000647561.1:c.914-8_947del
ENST00000322776.10:c.914-8_947del
ENST00000415352.6:c.893-8_926del
ENST00000526169.1:n.656-127_656-86del
ENST00000526770.5:n.1197-8_1230del
ENST00000527355.5:c.203-8_236del
ENST00000527923.1:n.248_289del
ENST00000529927.5:c.887-8_920del
ENST00000532303.5:c.611-8_644del
ENST00000533919.5:c.392-82_392-41del ENSP00000435199.1:n.392-82_392-41del
NM_001166102.1:c.887-8_920del
NM_007103.3:c.914-8_947del
NM_001166102.2:c.887-8_920del
NM_007103.4:c.914-8_947del