Canonical Allele Identifier: CA2351374371

Gene: NDUFAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801584G= , CM000682.2:g.13801584G=	GRCh38
NC_000020.10:g.13782230G= , CM000682.1:g.13782230G=	GRCh37
NC_000020.9:g.13730230G=	NCBI36
NG_015811.1:g.21559G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.618G= MANE Select	ENSP00000367346.5:p.Thr206=
ENST00000378081.9:c.618G=	ENSP00000437325.1:p.Thr206=
ENST00000378106.9:c.618G=	ENSP00000367346.5:p.Thr206=
ENST00000463598.1:c.534G=	ENSP00000420497.1:p.Thr178=
ENST00000464269.5:n.291G=
ENST00000475968.5:n.495G=
ENST00000476124.1:n.17G=
ENST00000476536.5:n.578G=
ENST00000477732.5:n.502+3084G=
ENST00000479716.5:n.139G=
ENST00000481249.5:n.495G=
ENST00000485738.5:n.595G=
ENST00000487478.5:n.42G=
NM_001039375.2:c.534G=	NP_001034464.1:p.Thr178=
NM_024120.4:c.618G=	NP_077025.2:p.Thr206=
NR_029377.1:n.661G=
XM_006723620.2:c.618G=	XP_006723683.1:p.Thr206=
XM_006723622.2:c.147G=	XP_006723685.1:p.Thr49=
XM_006723623.1:c.147G=	XP_006723686.1:p.Thr49=
XM_006723624.1:c.147G=	XP_006723687.1:p.Thr49=
XM_011529341.1:c.618G=	XP_011527643.1:p.Thr206=
XM_011529342.1:c.618G=	XP_011527644.1:p.Thr206=
XM_011529343.1:c.618G=	XP_011527645.1:p.Thr206=
XM_011529344.1:c.249G=	XP_011527646.1:p.Thr83=
XR_430269.2:n.638G=
XR_937140.1:n.638G=
NM_001352403.1:c.147G=	NP_001339332.1:p.Thr49=
NM_001352406.1:c.57G=	NP_001339335.1:p.Thr19=
NM_001352407.1:c.57G=	NP_001339336.1:p.Thr19=
NM_001352408.1:c.618G=	NP_001339337.1:p.Thr206=
NR_147978.1:n.661G=
NR_147979.1:n.681G=
NR_147980.1:n.557G=
NR_147981.1:n.795G=
NR_147982.1:n.795G=
NR_147983.1:n.711G=
XM_006723624.2:c.147G=	XP_006723687.1:p.Thr49=
XM_011529342.2:c.618G=	XP_011527644.1:p.Thr206=
XM_024451999.1:c.147G=	XP_024307767.1:p.Thr49=
XR_001754396.1:n.577G=
XR_430269.3:n.638G=
XR_937140.2:n.638G=
NM_024120.5:c.618G= MANE Select	NP_077025.2:p.Thr206=
NM_001039375.3:c.534G=	NP_001034464.1:p.Thr178=
NM_001352403.2:c.147G=	NP_001339332.1:p.Thr49=
NM_001352406.2:c.57G=	NP_001339335.1:p.Thr19=
NM_001352407.2:c.57G=	NP_001339336.1:p.Thr19=
NR_029377.2:n.659G=
NR_147978.2:n.659G=
NR_147979.2:n.679G=
NR_147980.2:n.555G=
NR_147981.2:n.793G=
NR_147982.2:n.793G=
NR_147983.2:n.709G=
NM_001352408.2:c.618G=	NP_001339337.1:p.Thr206=