Canonical Allele Identifier: CA2351374327

Gene: NDUFAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801493A= , CM000682.2:g.13801493A=	GRCh38
NC_000020.10:g.13782139A= , CM000682.1:g.13782139A=	GRCh37
NC_000020.9:g.13730139A=	NCBI36
NG_015811.1:g.21468A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.527A= MANE Select	ENSP00000367346.5:p.Tyr176=
ENST00000378081.9:c.527A=	ENSP00000437325.1:p.Tyr176=
ENST00000378106.9:c.527A=	ENSP00000367346.5:p.Tyr176=
ENST00000463598.1:c.443A=	ENSP00000420497.1:p.Tyr148=
ENST00000464269.5:n.200A=
ENST00000475968.5:n.404A=
ENST00000476536.5:n.487A=
ENST00000477732.5:n.502+2993A=
ENST00000479716.5:n.48A=
ENST00000481249.5:n.404A=
ENST00000485738.5:n.519-15A=
NM_001039375.2:c.443A=	NP_001034464.1:p.Tyr148=
NM_024120.4:c.527A=	NP_077025.2:p.Tyr176=
NR_029377.1:n.570A=
XM_006723620.2:c.527A=	XP_006723683.1:p.Tyr176=
XM_006723622.2:c.56A=	XP_006723685.1:p.Tyr19=
XM_006723623.1:c.56A=	XP_006723686.1:p.Tyr19=
XM_006723624.1:c.56A=	XP_006723687.1:p.Tyr19=
XM_011529341.1:c.527A=	XP_011527643.1:p.Tyr176=
XM_011529342.1:c.527A=	XP_011527644.1:p.Tyr176=
XM_011529343.1:c.527A=	XP_011527645.1:p.Tyr176=
XM_011529344.1:c.158A=	XP_011527646.1:p.Tyr53=
XR_430269.2:n.547A=
XR_937140.1:n.547A=
NM_001352403.1:c.56A=	NP_001339332.1:p.Tyr19=
NM_001352406.1:c.-35A=	NP_001339335.1:n.-35A=
NM_001352407.1:c.-35A=	NP_001339336.1:n.-35A=
NM_001352408.1:c.527A=	NP_001339337.1:p.Tyr176=
NR_147978.1:n.570A=
NR_147979.1:n.590A=
NR_147980.1:n.466A=
NR_147981.1:n.704A=
NR_147982.1:n.704A=
NR_147983.1:n.620A=
XM_006723624.2:c.56A=	XP_006723687.1:p.Tyr19=
XM_011529342.2:c.527A=	XP_011527644.1:p.Tyr176=
XM_024451999.1:c.56A=	XP_024307767.1:p.Tyr19=
XR_001754396.1:n.486A=
XR_430269.3:n.547A=
XR_937140.2:n.547A=
NM_024120.5:c.527A= MANE Select	NP_077025.2:p.Tyr176=
NM_001039375.3:c.443A=	NP_001034464.1:p.Tyr148=
NM_001352403.2:c.56A=	NP_001339332.1:p.Tyr19=
NM_001352406.2:c.-35A=	NP_001339335.1:n.-35A=
NM_001352407.2:c.-35A=	NP_001339336.1:n.-35A=
NR_029377.2:n.568A=
NR_147978.2:n.568A=
NR_147979.2:n.588A=
NR_147980.2:n.464A=
NR_147981.2:n.702A=
NR_147982.2:n.702A=
NR_147983.2:n.618A=
NM_001352408.2:c.527A=	NP_001339337.1:p.Tyr176=