Canonical Allele Identifier: CA2614649730
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611747_67611748insAA , CM000673.2:g.67611747_67611748insAA GRCh38
NC_000011.9:g.67379218_67379219insAA , CM000673.1:g.67379218_67379219insAA GRCh37
NC_000011.8:g.67135794_67135795insAA NCBI36
NG_013353.1:g.9896_9897insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000322776.11:c.1081-150_1081-149insAA MANE Select ENSP00000322450.6:n.1081-150_1081-149insAA
ENST00000647561.1:c.1081-150_1081-149insAA ENSP00000497587.1:n.1081-150_1081-149insAA
ENST00000322776.10:c.1081-150_1081-149insAA ENSP00000322450.6:n.1081-150_1081-149insAA
ENST00000415352.6:c.1060-150_1060-149insAA ENSP00000395368.2:n.1060-150_1060-149insAA
ENST00000526169.1:n.704-150_704-149insAA
ENST00000526770.5:n.1364-150_1364-149insAA
ENST00000527355.5:c.369+178_369+179insAA ENSP00000432637.1:n.369+178_369+179insAA
ENST00000527923.1:n.423-150_423-149insAA
ENST00000529927.5:c.1054-150_1054-149insAA ENSP00000436766.1:n.1054-150_1054-149insAA
ENST00000531250.1:n.195_196insAA
ENST00000532303.5:c.778-150_778-149insAA ENSP00000432015.1:n.778-150_778-149insAA
ENST00000533919.5:c.485-150_485-149insAA ENSP00000435199.1:n.485-150_485-149insAA
ENST00000534352.1:n.29_30insAA
NM_001166102.1:c.1054-150_1054-149insAA NP_001159574.1:n.1054-150_1054-149insAA
NM_007103.3:c.1081-150_1081-149insAA NP_009034.2:n.1081-150_1081-149insAA
NM_001166102.2:c.1054-150_1054-149insAA NP_001159574.1:n.1054-150_1054-149insAA
NM_007103.4:c.1081-150_1081-149insAA MANE Select NP_009034.2:n.1081-150_1081-149insAA