Canonical Allele Identifier: CA1980191651
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611394G= , CM000673.2:g.67611394G= GRCh38
NC_000011.9:g.67378865G= , CM000673.1:g.67378865G= GRCh37
NC_000011.8:g.67135441G= NCBI36
NG_013353.1:g.9543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.914-9G= MANE Select ENSP00000322450.6:n.914-9G=
ENST00000647561.1:c.914-9G= ENSP00000497587.1:n.914-9G=
ENST00000322776.10:c.914-9G= ENSP00000322450.6:n.914-9G=
ENST00000415352.6:c.893-9G= ENSP00000395368.2:n.893-9G=
ENST00000526169.1:n.656-128G=
ENST00000526770.5:n.1197-9G=
ENST00000527355.5:c.203-9G= ENSP00000432637.1:n.203-9G=
ENST00000527923.1:n.247G=
ENST00000529927.5:c.887-9G= ENSP00000436766.1:n.887-9G=
ENST00000532303.5:c.611-9G= ENSP00000432015.1:n.611-9G=
ENST00000533919.5:c.392-83G= ENSP00000435199.1:n.392-83G=
NM_001166102.1:c.887-9G= NP_001159574.1:n.887-9G=
NM_007103.3:c.914-9G= NP_009034.2:n.914-9G=
NM_001166102.2:c.887-9G= NP_001159574.1:n.887-9G=
NM_007103.4:c.914-9G= MANE Select NP_009034.2:n.914-9G=