Canonical Allele Identifier: CA1980190348
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610617G= , CM000673.2:g.67610617G= GRCh38
NC_000011.9:g.67378088G= , CM000673.1:g.67378088G= GRCh37
NC_000011.8:g.67134664G= NCBI36
NG_013353.1:g.8766G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.700+47G= MANE Select ENSP00000322450.6:n.700+47G=
ENST00000647561.1:c.700+47G= ENSP00000497587.1:n.700+47G=
ENST00000322776.10:c.700+47G= ENSP00000322450.6:n.700+47G=
ENST00000415352.6:c.679+47G= ENSP00000395368.2:n.679+47G=
ENST00000526169.1:n.442+47G=
ENST00000526770.5:n.606G=
ENST00000529927.5:c.673+47G= ENSP00000436766.1:n.673+47G=
ENST00000532303.5:c.397+47G= ENSP00000432015.1:n.397+47G=
ENST00000533919.5:c.178+47G= ENSP00000435199.1:n.178+47G=
NM_001166102.1:c.673+47G= NP_001159574.1:n.673+47G=
NM_007103.3:c.700+47G= NP_009034.2:n.700+47G=
NM_001166102.2:c.673+47G= NP_001159574.1:n.673+47G=
NM_007103.4:c.700+47G= MANE Select NP_009034.2:n.700+47G=