Canonical Allele Identifier: CA2351374328

Gene: NDUFAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801495A= , CM000682.2:g.13801495A=	GRCh38
NC_000020.10:g.13782141A= , CM000682.1:g.13782141A=	GRCh37
NC_000020.9:g.13730141A=	NCBI36
NG_015811.1:g.21470A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.529A= MANE Select	ENSP00000367346.5:p.Ile177=
ENST00000378081.9:c.529A=	ENSP00000437325.1:p.Ile177=
ENST00000378106.9:c.529A=	ENSP00000367346.5:p.Ile177=
ENST00000463598.1:c.445A=	ENSP00000420497.1:p.Ile149=
ENST00000464269.5:n.202A=
ENST00000475968.5:n.406A=
ENST00000476536.5:n.489A=
ENST00000477732.5:n.502+2995A=
ENST00000479716.5:n.50A=
ENST00000481249.5:n.406A=
ENST00000485738.5:n.519-13A=
NM_001039375.2:c.445A=	NP_001034464.1:p.Ile149=
NM_024120.4:c.529A=	NP_077025.2:p.Ile177=
NR_029377.1:n.572A=
XM_006723620.2:c.529A=	XP_006723683.1:p.Ile177=
XM_006723622.2:c.58A=	XP_006723685.1:p.Ile20=
XM_006723623.1:c.58A=	XP_006723686.1:p.Ile20=
XM_006723624.1:c.58A=	XP_006723687.1:p.Ile20=
XM_011529341.1:c.529A=	XP_011527643.1:p.Ile177=
XM_011529342.1:c.529A=	XP_011527644.1:p.Ile177=
XM_011529343.1:c.529A=	XP_011527645.1:p.Ile177=
XM_011529344.1:c.160A=	XP_011527646.1:p.Ile54=
XR_430269.2:n.549A=
XR_937140.1:n.549A=
NM_001352403.1:c.58A=	NP_001339332.1:p.Ile20=
NM_001352406.1:c.-33A=	NP_001339335.1:n.-33A=
NM_001352407.1:c.-33A=	NP_001339336.1:n.-33A=
NM_001352408.1:c.529A=	NP_001339337.1:p.Ile177=
NR_147978.1:n.572A=
NR_147979.1:n.592A=
NR_147980.1:n.468A=
NR_147981.1:n.706A=
NR_147982.1:n.706A=
NR_147983.1:n.622A=
XM_006723624.2:c.58A=	XP_006723687.1:p.Ile20=
XM_011529342.2:c.529A=	XP_011527644.1:p.Ile177=
XM_024451999.1:c.58A=	XP_024307767.1:p.Ile20=
XR_001754396.1:n.488A=
XR_430269.3:n.549A=
XR_937140.2:n.549A=
NM_024120.5:c.529A= MANE Select	NP_077025.2:p.Ile177=
NM_001039375.3:c.445A=	NP_001034464.1:p.Ile149=
NM_001352403.2:c.58A=	NP_001339332.1:p.Ile20=
NM_001352406.2:c.-33A=	NP_001339335.1:n.-33A=
NM_001352407.2:c.-33A=	NP_001339336.1:n.-33A=
NR_029377.2:n.570A=
NR_147978.2:n.570A=
NR_147979.2:n.590A=
NR_147980.2:n.466A=
NR_147981.2:n.704A=
NR_147982.2:n.704A=
NR_147983.2:n.620A=
NM_001352408.2:c.529A=	NP_001339337.1:p.Ile177=