Canonical Allele Identifier: CA939066121
Gene: NDUFV1 HGNC NCBI

Linked Data

dbSNP Id: rs758095599

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611862C>A , CM000673.2:g.67611862C>A GRCh38
NC_000011.9:g.67379333C>A , CM000673.1:g.67379333C>A GRCh37
NC_000011.8:g.67135909C>A NCBI36
NG_013353.1:g.10011C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1081-35C>A MANE Select ENSP00000322450.6:n.1081-35C>A
ENST00000647561.1:c.1081-35C>A ENSP00000497587.1:n.1081-35C>A
ENST00000322776.10:c.1081-35C>A ENSP00000322450.6:n.1081-35C>A
ENST00000415352.6:c.1060-35C>A ENSP00000395368.2:n.1060-35C>A
ENST00000526169.1:n.704-35C>A
ENST00000526770.5:n.1364-35C>A
ENST00000527355.5:c.370-258C>A ENSP00000432637.1:n.370-258C>A
ENST00000527923.1:n.423-35C>A
ENST00000529927.5:c.1054-35C>A ENSP00000436766.1:n.1054-35C>A
ENST00000531250.1:n.310C>A
ENST00000532303.5:c.778-35C>A ENSP00000432015.1:n.778-35C>A
ENST00000533919.5:c.485-35C>A ENSP00000435199.1:n.485-35C>A
ENST00000534352.1:n.144C>A
NM_001166102.1:c.1054-35C>A NP_001159574.1:n.1054-35C>A
NM_007103.3:c.1081-35C>A NP_009034.2:n.1081-35C>A
NM_001166102.2:c.1054-35C>A NP_001159574.1:n.1054-35C>A
NM_007103.4:c.1081-35C>A MANE Select NP_009034.2:n.1081-35C>A