Canonical Allele Identifier: CA2351374418

Gene: NDUFAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801704_13801705delinsAC , CM000682.2:g.13801704_13801705delinsAC	GRCh38
NC_000020.10:g.13782350_13782351delinsAC , CM000682.1:g.13782350_13782351delinsAC	GRCh37
NC_000020.9:g.13730350_13730351delinsAC	NCBI36
NG_015811.1:g.21679_21680delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.717+21_717+22delinsAC MANE Select	ENSP00000367346.5:n.717+21_717+22delinsAC
ENST00000378081.9:c.717+21_717+22delinsAC	ENSP00000437325.1:n.717+21_717+22delinsAC
ENST00000378106.9:c.717+21_717+22delinsAC	ENSP00000367346.5:n.717+21_717+22delinsAC
ENST00000463598.1:c.633+21_633+22delinsAC	ENSP00000420497.1:n.633+21_633+22delinsAC
ENST00000464269.5:n.390+21_390+22delinsAC
ENST00000475968.5:n.594+21_594+22delinsAC
ENST00000476124.1:n.116+21_116+22delinsAC
ENST00000476536.5:n.677+21_677+22delinsAC
ENST00000477732.5:n.502+3204_502+3205delinsAC
ENST00000479716.5:n.238+21_238+22delinsAC
ENST00000481249.5:n.594+21_594+22delinsAC
ENST00000485738.5:n.694+21_694+22delinsAC
ENST00000487478.5:n.141+21_141+22delinsAC
NM_001039375.2:c.633+21_633+22delinsAC	NP_001034464.1:n.633+21_633+22delinsAC
NM_024120.4:c.717+21_717+22delinsAC	NP_077025.2:n.717+21_717+22delinsAC
NR_029377.1:n.760+21_760+22delinsAC
XM_006723620.2:c.717+21_717+22delinsAC	XP_006723683.1:n.717+21_717+22delinsAC
XM_006723622.2:c.246+21_246+22delinsAC	XP_006723685.1:n.246+21_246+22delinsAC
XM_006723623.1:c.246+21_246+22delinsAC	XP_006723686.1:n.246+21_246+22delinsAC
XM_006723624.1:c.246+21_246+22delinsAC	XP_006723687.1:n.246+21_246+22delinsAC
XM_011529341.1:c.717+21_717+22delinsAC	XP_011527643.1:n.717+21_717+22delinsAC
XM_011529342.1:c.717+21_717+22delinsAC	XP_011527644.1:n.717+21_717+22delinsAC
XM_011529343.1:c.717+21_717+22delinsAC	XP_011527645.1:n.717+21_717+22delinsAC
XM_011529344.1:c.348+21_348+22delinsAC	XP_011527646.1:n.348+21_348+22delinsAC
XR_430269.2:n.737+21_737+22delinsAC
XR_937140.1:n.737+21_737+22delinsAC
NM_001352403.1:c.246+21_246+22delinsAC	NP_001339332.1:n.246+21_246+22delinsAC
NM_001352406.1:c.156+21_156+22delinsAC	NP_001339335.1:n.156+21_156+22delinsAC
NM_001352407.1:c.156+21_156+22delinsAC	NP_001339336.1:n.156+21_156+22delinsAC
NM_001352408.1:c.717+21_717+22delinsAC	NP_001339337.1:n.717+21_717+22delinsAC
NR_147978.1:n.760+21_760+22delinsAC
NR_147979.1:n.780+21_780+22delinsAC
NR_147980.1:n.656+21_656+22delinsAC
NR_147981.1:n.894+21_894+22delinsAC
NR_147982.1:n.894+21_894+22delinsAC
NR_147983.1:n.810+21_810+22delinsAC
XM_006723624.2:c.246+21_246+22delinsAC	XP_006723687.1:n.246+21_246+22delinsAC
XM_011529342.2:c.717+21_717+22delinsAC	XP_011527644.1:n.717+21_717+22delinsAC
XM_024451999.1:c.246+21_246+22delinsAC	XP_024307767.1:n.246+21_246+22delinsAC
XR_001754396.1:n.676+21_676+22delinsAC
XR_430269.3:n.737+21_737+22delinsAC
XR_937140.2:n.737+21_737+22delinsAC
NM_024120.5:c.717+21_717+22delinsAC MANE Select	NP_077025.2:n.717+21_717+22delinsAC
NM_001039375.3:c.633+21_633+22delinsAC	NP_001034464.1:n.633+21_633+22delinsAC
NM_001352403.2:c.246+21_246+22delinsAC	NP_001339332.1:n.246+21_246+22delinsAC
NM_001352406.2:c.156+21_156+22delinsAC	NP_001339335.1:n.156+21_156+22delinsAC
NM_001352407.2:c.156+21_156+22delinsAC	NP_001339336.1:n.156+21_156+22delinsAC
NR_029377.2:n.758+21_758+22delinsAC
NR_147978.2:n.758+21_758+22delinsAC
NR_147979.2:n.778+21_778+22delinsAC
NR_147980.2:n.654+21_654+22delinsAC
NR_147981.2:n.892+21_892+22delinsAC
NR_147982.2:n.892+21_892+22delinsAC
NR_147983.2:n.808+21_808+22delinsAC
NM_001352408.2:c.717+21_717+22delinsAC	NP_001339337.1:n.717+21_717+22delinsAC