Canonical Allele Identifier: CA408270914

Gene: NDUFAF5

Linked Data

• MyVariant Identifiers: chr20:g.13782246T>G (hg19) ; chr20:g.13801600T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801600T>G , CM000682.2:g.13801600T>G	GRCh38
NC_000020.10:g.13782246T>G , CM000682.1:g.13782246T>G	GRCh37
NC_000020.9:g.13730246T>G	NCBI36
NG_015811.1:g.21575T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.634T>G MANE Select	ENSP00000367346.5:p.Phe212Val
ENST00000378081.9:c.634T>G	ENSP00000437325.1:p.Phe212Val
ENST00000378106.9:c.634T>G	ENSP00000367346.5:p.Phe212Val
ENST00000463598.1:c.550T>G	ENSP00000420497.1:p.Phe184Val
ENST00000464269.5:n.307T>G
ENST00000475968.5:n.511T>G
ENST00000476124.1:n.33T>G
ENST00000476536.5:n.594T>G
ENST00000477732.5:n.502+3100T>G
ENST00000479716.5:n.155T>G
ENST00000481249.5:n.511T>G
ENST00000485738.5:n.611T>G
ENST00000487478.5:n.58T>G
NM_001039375.2:c.550T>G	NP_001034464.1:p.Phe184Val
NM_024120.4:c.634T>G	NP_077025.2:p.Phe212Val
NR_029377.1:n.677T>G
XM_006723620.2:c.634T>G	XP_006723683.1:p.Phe212Val
XM_006723622.2:c.163T>G	XP_006723685.1:p.Phe55Val
XM_006723623.1:c.163T>G	XP_006723686.1:p.Phe55Val
XM_006723624.1:c.163T>G	XP_006723687.1:p.Phe55Val
XM_011529341.1:c.634T>G	XP_011527643.1:p.Phe212Val
XM_011529342.1:c.634T>G	XP_011527644.1:p.Phe212Val
XM_011529343.1:c.634T>G	XP_011527645.1:p.Phe212Val
XM_011529344.1:c.265T>G	XP_011527646.1:p.Phe89Val
XR_430269.2:n.654T>G
XR_937140.1:n.654T>G
NM_001352403.1:c.163T>G	NP_001339332.1:p.Phe55Val
NM_001352406.1:c.73T>G	NP_001339335.1:p.Phe25Val
NM_001352407.1:c.73T>G	NP_001339336.1:p.Phe25Val
NM_001352408.1:c.634T>G	NP_001339337.1:p.Phe212Val
NR_147978.1:n.677T>G
NR_147979.1:n.697T>G
NR_147980.1:n.573T>G
NR_147981.1:n.811T>G
NR_147982.1:n.811T>G
NR_147983.1:n.727T>G
XM_006723624.2:c.163T>G	XP_006723687.1:p.Phe55Val
XM_011529342.2:c.634T>G	XP_011527644.1:p.Phe212Val
XM_024451999.1:c.163T>G	XP_024307767.1:p.Phe55Val
XR_001754396.1:n.593T>G
XR_430269.3:n.654T>G
XR_937140.2:n.654T>G
NM_024120.5:c.634T>G MANE Select	NP_077025.2:p.Phe212Val
NM_001039375.3:c.550T>G	NP_001034464.1:p.Phe184Val
NM_001352403.2:c.163T>G	NP_001339332.1:p.Phe55Val
NM_001352406.2:c.73T>G	NP_001339335.1:p.Phe25Val
NM_001352407.2:c.73T>G	NP_001339336.1:p.Phe25Val
NR_029377.2:n.675T>G
NR_147978.2:n.675T>G
NR_147979.2:n.695T>G
NR_147980.2:n.571T>G
NR_147981.2:n.809T>G
NR_147982.2:n.809T>G
NR_147983.2:n.725T>G
NM_001352408.2:c.634T>G	NP_001339337.1:p.Phe212Val