Canonical Allele Identifier: CA1980190311
Gene: NDUFV1 HGNC NCBI

Linked Data

dbSNP Id: rs1391487188

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67610605C>G , CM000673.2:g.67610605C>G GRCh38
NC_000011.9:g.67378076C>G , CM000673.1:g.67378076C>G GRCh37
NC_000011.8:g.67134652C>G NCBI36
NG_013353.1:g.8754C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.700+35C>G MANE Select ENSP00000322450.6:n.700+35C>G
ENST00000647561.1:c.700+35C>G ENSP00000497587.1:n.700+35C>G
ENST00000322776.10:c.700+35C>G ENSP00000322450.6:n.700+35C>G
ENST00000415352.6:c.679+35C>G ENSP00000395368.2:n.679+35C>G
ENST00000526169.1:n.442+35C>G
ENST00000526770.5:n.594C>G
ENST00000529927.5:c.673+35C>G ENSP00000436766.1:n.673+35C>G
ENST00000532303.5:c.397+35C>G ENSP00000432015.1:n.397+35C>G
ENST00000533919.5:c.178+35C>G ENSP00000435199.1:n.178+35C>G
NM_001166102.1:c.673+35C>G NP_001159574.1:n.673+35C>G
NM_007103.3:c.700+35C>G NP_009034.2:n.700+35C>G
NM_001166102.2:c.673+35C>G NP_001159574.1:n.673+35C>G
NM_007103.4:c.700+35C>G MANE Select NP_009034.2:n.700+35C>G