Canonical Allele Identifier: CA509676269

Gene: NDUFAF5

Linked Data

• MyVariant Identifiers: chr20:g.13782314T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801668T>C , CM000682.2:g.13801668T>C	GRCh38
NC_000020.10:g.13782314T>C , CM000682.1:g.13782314T>C	GRCh37
NC_000020.9:g.13730314T>C	NCBI36
NG_015811.1:g.21643T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.702T>C MANE Select	ENSP00000367346.5:p.Phe234=
ENST00000378081.9:c.702T>C	ENSP00000437325.1:p.Phe234=
ENST00000378106.9:c.702T>C	ENSP00000367346.5:p.Phe234=
ENST00000463598.1:c.618T>C	ENSP00000420497.1:p.Phe206=
ENST00000464269.5:n.375T>C
ENST00000475968.5:n.579T>C
ENST00000476124.1:n.101T>C
ENST00000476536.5:n.662T>C
ENST00000477732.5:n.502+3168T>C
ENST00000479716.5:n.223T>C
ENST00000481249.5:n.579T>C
ENST00000485738.5:n.679T>C
ENST00000487478.5:n.126T>C
NM_001039375.2:c.618T>C	NP_001034464.1:p.Phe206=
NM_024120.4:c.702T>C	NP_077025.2:p.Phe234=
NR_029377.1:n.745T>C
XM_006723620.2:c.702T>C	XP_006723683.1:p.Phe234=
XM_006723622.2:c.231T>C	XP_006723685.1:p.Phe77=
XM_006723623.1:c.231T>C	XP_006723686.1:p.Phe77=
XM_006723624.1:c.231T>C	XP_006723687.1:p.Phe77=
XM_011529341.1:c.702T>C	XP_011527643.1:p.Phe234=
XM_011529342.1:c.702T>C	XP_011527644.1:p.Phe234=
XM_011529343.1:c.702T>C	XP_011527645.1:p.Phe234=
XM_011529344.1:c.333T>C	XP_011527646.1:p.Phe111=
XR_430269.2:n.722T>C
XR_937140.1:n.722T>C
NM_001352403.1:c.231T>C	NP_001339332.1:p.Phe77=
NM_001352406.1:c.141T>C	NP_001339335.1:p.Phe47=
NM_001352407.1:c.141T>C	NP_001339336.1:p.Phe47=
NM_001352408.1:c.702T>C	NP_001339337.1:p.Phe234=
NR_147978.1:n.745T>C
NR_147979.1:n.765T>C
NR_147980.1:n.641T>C
NR_147981.1:n.879T>C
NR_147982.1:n.879T>C
NR_147983.1:n.795T>C
XM_006723624.2:c.231T>C	XP_006723687.1:p.Phe77=
XM_011529342.2:c.702T>C	XP_011527644.1:p.Phe234=
XM_024451999.1:c.231T>C	XP_024307767.1:p.Phe77=
XR_001754396.1:n.661T>C
XR_430269.3:n.722T>C
XR_937140.2:n.722T>C
NM_024120.5:c.702T>C MANE Select	NP_077025.2:p.Phe234=
NM_001039375.3:c.618T>C	NP_001034464.1:p.Phe206=
NM_001352403.2:c.231T>C	NP_001339332.1:p.Phe77=
NM_001352406.2:c.141T>C	NP_001339335.1:p.Phe47=
NM_001352407.2:c.141T>C	NP_001339336.1:p.Phe47=
NR_029377.2:n.743T>C
NR_147978.2:n.743T>C
NR_147979.2:n.763T>C
NR_147980.2:n.639T>C
NR_147981.2:n.877T>C
NR_147982.2:n.877T>C
NR_147983.2:n.793T>C
NM_001352408.2:c.702T>C	NP_001339337.1:p.Phe234=