Canonical Allele Identifier: CA509675896

Gene: NDUFAF5

Linked Data

• MyVariant Identifiers: chr20:g.13782251T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801605T>A , CM000682.2:g.13801605T>A	GRCh38
NC_000020.10:g.13782251T>A , CM000682.1:g.13782251T>A	GRCh37
NC_000020.9:g.13730251T>A	NCBI36
NG_015811.1:g.21580T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.639T>A MANE Select	ENSP00000367346.5:p.Ser213=
ENST00000378081.9:c.639T>A	ENSP00000437325.1:p.Ser213=
ENST00000378106.9:c.639T>A	ENSP00000367346.5:p.Ser213=
ENST00000463598.1:c.555T>A	ENSP00000420497.1:p.Ser185=
ENST00000464269.5:n.312T>A
ENST00000475968.5:n.516T>A
ENST00000476124.1:n.38T>A
ENST00000476536.5:n.599T>A
ENST00000477732.5:n.502+3105T>A
ENST00000479716.5:n.160T>A
ENST00000481249.5:n.516T>A
ENST00000485738.5:n.616T>A
ENST00000487478.5:n.63T>A
NM_001039375.2:c.555T>A	NP_001034464.1:p.Ser185=
NM_024120.4:c.639T>A	NP_077025.2:p.Ser213=
NR_029377.1:n.682T>A
XM_006723620.2:c.639T>A	XP_006723683.1:p.Ser213=
XM_006723622.2:c.168T>A	XP_006723685.1:p.Ser56=
XM_006723623.1:c.168T>A	XP_006723686.1:p.Ser56=
XM_006723624.1:c.168T>A	XP_006723687.1:p.Ser56=
XM_011529341.1:c.639T>A	XP_011527643.1:p.Ser213=
XM_011529342.1:c.639T>A	XP_011527644.1:p.Ser213=
XM_011529343.1:c.639T>A	XP_011527645.1:p.Ser213=
XM_011529344.1:c.270T>A	XP_011527646.1:p.Ser90=
XR_430269.2:n.659T>A
XR_937140.1:n.659T>A
NM_001352403.1:c.168T>A	NP_001339332.1:p.Ser56=
NM_001352406.1:c.78T>A	NP_001339335.1:p.Ser26=
NM_001352407.1:c.78T>A	NP_001339336.1:p.Ser26=
NM_001352408.1:c.639T>A	NP_001339337.1:p.Ser213=
NR_147978.1:n.682T>A
NR_147979.1:n.702T>A
NR_147980.1:n.578T>A
NR_147981.1:n.816T>A
NR_147982.1:n.816T>A
NR_147983.1:n.732T>A
XM_006723624.2:c.168T>A	XP_006723687.1:p.Ser56=
XM_011529342.2:c.639T>A	XP_011527644.1:p.Ser213=
XM_024451999.1:c.168T>A	XP_024307767.1:p.Ser56=
XR_001754396.1:n.598T>A
XR_430269.3:n.659T>A
XR_937140.2:n.659T>A
NM_024120.5:c.639T>A MANE Select	NP_077025.2:p.Ser213=
NM_001039375.3:c.555T>A	NP_001034464.1:p.Ser185=
NM_001352403.2:c.168T>A	NP_001339332.1:p.Ser56=
NM_001352406.2:c.78T>A	NP_001339335.1:p.Ser26=
NM_001352407.2:c.78T>A	NP_001339336.1:p.Ser26=
NR_029377.2:n.680T>A
NR_147978.2:n.680T>A
NR_147979.2:n.700T>A
NR_147980.2:n.576T>A
NR_147981.2:n.814T>A
NR_147982.2:n.814T>A
NR_147983.2:n.730T>A
NM_001352408.2:c.639T>A	NP_001339337.1:p.Ser213=