Canonical Allele Identifier: CA381541302
Gene: NDUFV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67611898C>A , CM000673.2:g.67611898C>A GRCh38
NC_000011.9:g.67379369C>A , CM000673.1:g.67379369C>A GRCh37
NC_000011.8:g.67135945C>A NCBI36
NG_013353.1:g.10047C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322776.11:c.1082C>A MANE Select ENSP00000322450.6:p.Thr361Lys
ENST00000647561.1:c.1082C>A ENSP00000497587.1:p.Thr361Lys
ENST00000322776.10:c.1082C>A ENSP00000322450.6:p.Thr361Lys
ENST00000415352.6:c.1061C>A ENSP00000395368.2:p.Thr354Lys
ENST00000526169.1:n.705C>A
ENST00000526770.5:n.1365C>A
ENST00000527355.5:c.370-222C>A ENSP00000432637.1:n.370-222C>A
ENST00000527923.1:n.424C>A
ENST00000529927.5:c.1055C>A ENSP00000436766.1:p.Thr352Lys
ENST00000531250.1:n.346C>A
ENST00000532303.5:c.779C>A ENSP00000432015.1:p.Thr260Lys
ENST00000533919.5:c.486C>A ENSP00000435199.1:n.486C>A
ENST00000534352.1:n.180C>A
NM_001166102.1:c.1055C>A NP_001159574.1:p.Thr352Lys
NM_007103.3:c.1082C>A NP_009034.2:p.Thr361Lys
NM_001166102.2:c.1055C>A NP_001159574.1:p.Thr352Lys
NM_007103.4:c.1082C>A MANE Select NP_009034.2:p.Thr361Lys