Canonical Allele Identifier: CA2739277077
Gene: NDUFAF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2808216
ClinVar RCV Id: RCV003684745

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13801676dup , CM000682.2:g.13801676dup GRCh38
NC_000020.10:g.13782322dup , CM000682.1:g.13782322dup GRCh37
NC_000020.9:g.13730322dup NCBI36
NG_015811.1:g.21651dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378106.10:c.710dup MANE Select ENSP00000367346.5:p.Thr238AspfsTer5
ENST00000378081.9:c.710dup ENSP00000437325.1:p.Thr238AspfsTer5
ENST00000378106.9:c.710dup ENSP00000367346.5:p.Thr238AspfsTer5
ENST00000463598.1:c.626dup ENSP00000420497.1:p.Thr210AspfsTer5
ENST00000464269.5:n.383dup
ENST00000475968.5:n.587dup
ENST00000476124.1:n.109dup
ENST00000476536.5:n.670dup
ENST00000477732.5:n.502+3176dup
ENST00000479716.5:n.231dup
ENST00000481249.5:n.587dup
ENST00000485738.5:n.687dup
ENST00000487478.5:n.134dup
NM_001039375.2:c.626dup NP_001034464.1:p.Thr210AspfsTer5
NM_024120.4:c.710dup NP_077025.2:p.Thr238AspfsTer5
NR_029377.1:n.753dup
XM_006723620.2:c.710dup XP_006723683.1:p.Thr238AspfsTer8
XM_006723622.2:c.239dup XP_006723685.1:p.Thr81AspfsTer5
XM_006723623.1:c.239dup XP_006723686.1:p.Thr81AspfsTer5
XM_006723624.1:c.239dup XP_006723687.1:p.Thr81AspfsTer5
XM_011529341.1:c.710dup XP_011527643.1:p.Thr238AspfsTer5
XM_011529342.1:c.710dup XP_011527644.1:p.Thr238AspfsTer13
XM_011529343.1:c.710dup XP_011527645.1:p.Thr238AspfsTer5
XM_011529344.1:c.341dup XP_011527646.1:p.Thr115AspfsTer5
XR_430269.2:n.730dup
XR_937140.1:n.730dup
NM_001352403.1:c.239dup NP_001339332.1:p.Thr81AspfsTer5
NM_001352406.1:c.149dup NP_001339335.1:p.Thr51AspfsTer5
NM_001352407.1:c.149dup NP_001339336.1:p.Thr51AspfsTer5
NM_001352408.1:c.710dup NP_001339337.1:p.Thr238AspfsTer8
NR_147978.1:n.753dup
NR_147979.1:n.773dup
NR_147980.1:n.649dup
NR_147981.1:n.887dup
NR_147982.1:n.887dup
NR_147983.1:n.803dup
XM_006723624.2:c.239dup XP_006723687.1:p.Thr81AspfsTer5
XM_011529342.2:c.710dup XP_011527644.1:p.Thr238AspfsTer13
XM_024451999.1:c.239dup XP_024307767.1:p.Thr81AspfsTer5
XR_001754396.1:n.669dup
XR_430269.3:n.730dup
XR_937140.2:n.730dup
NM_024120.5:c.710dup MANE Select NP_077025.2:p.Thr238AspfsTer5
NM_001039375.3:c.626dup NP_001034464.1:p.Thr210AspfsTer5
NM_001352403.2:c.239dup NP_001339332.1:p.Thr81AspfsTer5
NM_001352406.2:c.149dup NP_001339335.1:p.Thr51AspfsTer5
NM_001352407.2:c.149dup NP_001339336.1:p.Thr51AspfsTer5
NR_029377.2:n.751dup
NR_147978.2:n.751dup
NR_147979.2:n.771dup
NR_147980.2:n.647dup
NR_147981.2:n.885dup
NR_147982.2:n.885dup
NR_147983.2:n.801dup
NM_001352408.2:c.710dup NP_001339337.1:p.Thr238AspfsTer8