Canonical Allele Identifier: CA2351374185

Gene: NDUFAF5

Linked Data

• dbSNP Id: rs1984055457

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801137_13801138insACGTTTC , CM000682.2:g.13801137_13801138insACGTTTC	GRCh38
NC_000020.10:g.13781783_13781784insACGTTTC , CM000682.1:g.13781783_13781784insACGTTTC	GRCh37
NC_000020.9:g.13729783_13729784insACGTTTC	NCBI36
NG_015811.1:g.21112_21113insACGTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.520-349_520-348insACGTTTC MANE Select	ENSP00000367346.5:n.520-349_520-348insACGTTTC
ENST00000378081.9:c.520-349_520-348insACGTTTC	ENSP00000437325.1:n.520-349_520-348insACGTTTC
ENST00000378106.9:c.520-349_520-348insACGTTTC	ENSP00000367346.5:n.520-349_520-348insACGTTTC
ENST00000463598.1:c.436-349_436-348insACGTTTC	ENSP00000420497.1:n.436-349_436-348insACGTTTC
ENST00000464269.5:n.193-349_193-348insACGTTTC
ENST00000475968.5:n.397-349_397-348insACGTTTC
ENST00000476536.5:n.480-349_480-348insACGTTTC
ENST00000477732.5:n.502+2637_502+2638insACGTTTC
ENST00000479716.5:n.41-349_41-348insACGTTTC
ENST00000481249.5:n.397-349_397-348insACGTTTC
ENST00000485738.5:n.519-371_519-370insACGTTTC
NM_001039375.2:c.436-349_436-348insACGTTTC	NP_001034464.1:n.436-349_436-348insACGTTTC
NM_024120.4:c.520-349_520-348insACGTTTC	NP_077025.2:n.520-349_520-348insACGTTTC
NR_029377.1:n.563-349_563-348insACGTTTC
XM_006723620.2:c.520-349_520-348insACGTTTC	XP_006723683.1:n.520-349_520-348insACGTTTC
XM_006723622.2:c.49-349_49-348insACGTTTC	XP_006723685.1:n.49-349_49-348insACGTTTC
XM_006723623.1:c.49-349_49-348insACGTTTC	XP_006723686.1:n.49-349_49-348insACGTTTC
XM_006723624.1:c.49-349_49-348insACGTTTC	XP_006723687.1:n.49-349_49-348insACGTTTC
XM_011529341.1:c.520-349_520-348insACGTTTC	XP_011527643.1:n.520-349_520-348insACGTTTC
XM_011529342.1:c.520-349_520-348insACGTTTC	XP_011527644.1:n.520-349_520-348insACGTTTC
XM_011529343.1:c.520-349_520-348insACGTTTC	XP_011527645.1:n.520-349_520-348insACGTTTC
XM_011529344.1:c.151-349_151-348insACGTTTC	XP_011527646.1:n.151-349_151-348insACGTTTC
XR_430269.2:n.540-349_540-348insACGTTTC
XR_937140.1:n.540-349_540-348insACGTTTC
NM_001352403.1:c.49-349_49-348insACGTTTC	NP_001339332.1:n.49-349_49-348insACGTTTC
NM_001352406.1:c.-42-349_-42-348insACGTTTC	NP_001339335.1:n.-42-349_-42-348insACGTTTC
NM_001352407.1:c.-42-349_-42-348insACGTTTC	NP_001339336.1:n.-42-349_-42-348insACGTTTC
NM_001352408.1:c.520-349_520-348insACGTTTC	NP_001339337.1:n.520-349_520-348insACGTTTC
NR_147978.1:n.563-349_563-348insACGTTTC
NR_147979.1:n.583-349_583-348insACGTTTC
NR_147980.1:n.459-349_459-348insACGTTTC
NR_147981.1:n.697-349_697-348insACGTTTC
NR_147982.1:n.697-349_697-348insACGTTTC
NR_147983.1:n.613-349_613-348insACGTTTC
XM_006723624.2:c.49-349_49-348insACGTTTC	XP_006723687.1:n.49-349_49-348insACGTTTC
XM_011529342.2:c.520-349_520-348insACGTTTC	XP_011527644.1:n.520-349_520-348insACGTTTC
XM_024451999.1:c.49-349_49-348insACGTTTC	XP_024307767.1:n.49-349_49-348insACGTTTC
XR_001754396.1:n.479-349_479-348insACGTTTC
XR_430269.3:n.540-349_540-348insACGTTTC
XR_937140.2:n.540-349_540-348insACGTTTC
NM_024120.5:c.520-349_520-348insACGTTTC MANE Select	NP_077025.2:n.520-349_520-348insACGTTTC
NM_001039375.3:c.436-349_436-348insACGTTTC	NP_001034464.1:n.436-349_436-348insACGTTTC
NM_001352403.2:c.49-349_49-348insACGTTTC	NP_001339332.1:n.49-349_49-348insACGTTTC
NM_001352406.2:c.-42-349_-42-348insACGTTTC	NP_001339335.1:n.-42-349_-42-348insACGTTTC
NM_001352407.2:c.-42-349_-42-348insACGTTTC	NP_001339336.1:n.-42-349_-42-348insACGTTTC
NR_029377.2:n.561-349_561-348insACGTTTC
NR_147978.2:n.561-349_561-348insACGTTTC
NR_147979.2:n.581-349_581-348insACGTTTC
NR_147980.2:n.457-349_457-348insACGTTTC
NR_147981.2:n.695-349_695-348insACGTTTC
NR_147982.2:n.695-349_695-348insACGTTTC
NR_147983.2:n.611-349_611-348insACGTTTC
NM_001352408.2:c.520-349_520-348insACGTTTC	NP_001339337.1:n.520-349_520-348insACGTTTC