Canonical Allele Identifier: CA324776

Gene: NDUFAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13785068G>C , CM000682.2:g.13785068G>C	GRCh38
NC_000020.10:g.13765714G>C , CM000682.1:g.13765714G>C	GRCh37
NC_000020.9:g.13713714G>C	NCBI36
NG_015811.1:g.5043G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024120.5:c.-1G>C MANE Select	NP_077025.2:n.-1G>C
ENST00000378106.10:c.-1G>C MANE Select	ENSP00000367346.5:n.-1G>C
NM_001039375.2:c.-1G>C	NP_001034464.1:n.-1G>C
NM_001039375.3:c.-1G>C	NP_001034464.1:n.-1G>C
NM_001352403.1:c.-368G>C	NP_001339332.1:n.-368G>C
NM_001352403.2:c.-368G>C	NP_001339332.1:n.-368G>C
NM_001352406.1:c.-582G>C	NP_001339335.1:n.-582G>C
NM_001352406.2:c.-582G>C	NP_001339335.1:n.-582G>C
NM_001352407.1:c.-696G>C	NP_001339336.1:n.-696G>C
NM_001352407.2:c.-696G>C	NP_001339336.1:n.-696G>C
NM_001352408.1:c.-1G>C	NP_001339337.1:n.-1G>C
NM_001352408.2:c.-1G>C	NP_001339337.1:n.-1G>C
NM_024120.4:c.-1G>C	NP_077025.2:n.-1G>C
NR_029377.1:n.43G>C
NR_029377.2:n.41G>C
NR_147978.1:n.43G>C
NR_147978.2:n.41G>C
NR_147979.1:n.43G>C
NR_147979.2:n.41G>C
NR_147980.1:n.43G>C
NR_147980.2:n.41G>C
NR_147981.1:n.43G>C
NR_147981.2:n.41G>C
NR_147982.1:n.43G>C
NR_147982.2:n.41G>C
NR_147983.1:n.43G>C
NR_147983.2:n.41G>C
ENST00000378081.9:c.-1G>C	ENSP00000437325.1:n.-1G>C
ENST00000378106.9:c.-1G>C	ENSP00000367346.5:n.-1G>C
ENST00000463598.1:c.-1G>C	ENSP00000420497.1:n.-1G>C
XM_006723620.2:c.-1G>C	XP_006723683.1:n.-1G>C
XM_006723622.2:c.-368G>C	XP_006723685.1:n.-368G>C
XM_006723623.1:c.-522G>C	XP_006723686.1:n.-522G>C
XM_006723624.1:c.-502G>C	XP_006723687.1:n.-502G>C
XM_006723624.2:c.-502G>C	XP_006723687.1:n.-502G>C
XM_011529341.1:c.-1G>C	XP_011527643.1:n.-1G>C
XM_011529342.1:c.-1G>C	XP_011527644.1:n.-1G>C
XM_011529342.2:c.-1G>C	XP_011527644.1:n.-1G>C
XM_011529343.1:c.-1G>C	XP_011527645.1:n.-1G>C
XR_001754396.1:n.43G>C
XR_430269.2:n.20G>C
XR_430269.3:n.20G>C
XR_937140.1:n.20G>C
XR_937140.2:n.20G>C