Canonical Allele Identifier: CA2839651943
Gene: NDUFV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611589C>A , CM000673.2:g.67611589C>A GRCh38
NC_000011.9:g.67379060C>A , CM000673.1:g.67379060C>A GRCh37
NC_000011.8:g.67135636C>A NCBI36
NG_013353.1:g.9738C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1080+20C>A MANE Select ENSP00000322450.6:n.1080+20C>A
ENST00000647561.1:c.1080+20C>A ENSP00000497587.1:n.1080+20C>A
ENST00000322776.10:c.1080+20C>A ENSP00000322450.6:n.1080+20C>A
ENST00000415352.6:c.1059+20C>A ENSP00000395368.2:n.1059+20C>A
ENST00000526169.1:n.703+20C>A
ENST00000526770.5:n.1363+20C>A
ENST00000527355.5:c.369+20C>A ENSP00000432637.1:n.369+20C>A
ENST00000527923.1:n.422+20C>A
ENST00000529927.5:c.1053+20C>A ENSP00000436766.1:n.1053+20C>A
ENST00000531250.1:n.37C>A
ENST00000532303.5:c.777+20C>A ENSP00000432015.1:n.777+20C>A
ENST00000533919.5:c.484+20C>A ENSP00000435199.1:n.484+20C>A
NM_001166102.1:c.1053+20C>A NP_001159574.1:n.1053+20C>A
NM_007103.3:c.1080+20C>A NP_009034.2:n.1080+20C>A
NM_001166102.2:c.1053+20C>A NP_001159574.1:n.1053+20C>A
NM_007103.4:c.1080+20C>A MANE Select NP_009034.2:n.1080+20C>A