Canonical Allele Identifier: CA408270761

Gene: NDUFAF5

Linked Data

• MyVariant Identifiers: chr20:g.13782205G>C (hg19) ; chr20:g.13801559G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801559G>C , CM000682.2:g.13801559G>C	GRCh38
NC_000020.10:g.13782205G>C , CM000682.1:g.13782205G>C	GRCh37
NC_000020.9:g.13730205G>C	NCBI36
NG_015811.1:g.21534G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378106.10:c.593G>C MANE Select	ENSP00000367346.5:p.Arg198Pro
ENST00000378081.9:c.593G>C	ENSP00000437325.1:p.Arg198Pro
ENST00000378106.9:c.593G>C	ENSP00000367346.5:p.Arg198Pro
ENST00000463598.1:c.509G>C	ENSP00000420497.1:p.Arg170Pro
ENST00000464269.5:n.266G>C
ENST00000475968.5:n.470G>C
ENST00000476536.5:n.553G>C
ENST00000477732.5:n.502+3059G>C
ENST00000479716.5:n.114G>C
ENST00000481249.5:n.470G>C
ENST00000485738.5:n.570G>C
ENST00000487478.5:n.17G>C
NM_001039375.2:c.509G>C	NP_001034464.1:p.Arg170Pro
NM_024120.4:c.593G>C	NP_077025.2:p.Arg198Pro
NR_029377.1:n.636G>C
XM_006723620.2:c.593G>C	XP_006723683.1:p.Arg198Pro
XM_006723622.2:c.122G>C	XP_006723685.1:p.Arg41Pro
XM_006723623.1:c.122G>C	XP_006723686.1:p.Arg41Pro
XM_006723624.1:c.122G>C	XP_006723687.1:p.Arg41Pro
XM_011529341.1:c.593G>C	XP_011527643.1:p.Arg198Pro
XM_011529342.1:c.593G>C	XP_011527644.1:p.Arg198Pro
XM_011529343.1:c.593G>C	XP_011527645.1:p.Arg198Pro
XM_011529344.1:c.224G>C	XP_011527646.1:p.Arg75Pro
XR_430269.2:n.613G>C
XR_937140.1:n.613G>C
NM_001352403.1:c.122G>C	NP_001339332.1:p.Arg41Pro
NM_001352406.1:c.32G>C	NP_001339335.1:p.Arg11Pro
NM_001352407.1:c.32G>C	NP_001339336.1:p.Arg11Pro
NM_001352408.1:c.593G>C	NP_001339337.1:p.Arg198Pro
NR_147978.1:n.636G>C
NR_147979.1:n.656G>C
NR_147980.1:n.532G>C
NR_147981.1:n.770G>C
NR_147982.1:n.770G>C
NR_147983.1:n.686G>C
XM_006723624.2:c.122G>C	XP_006723687.1:p.Arg41Pro
XM_011529342.2:c.593G>C	XP_011527644.1:p.Arg198Pro
XM_024451999.1:c.122G>C	XP_024307767.1:p.Arg41Pro
XR_001754396.1:n.552G>C
XR_430269.3:n.613G>C
XR_937140.2:n.613G>C
NM_024120.5:c.593G>C MANE Select	NP_077025.2:p.Arg198Pro
NM_001039375.3:c.509G>C	NP_001034464.1:p.Arg170Pro
NM_001352403.2:c.122G>C	NP_001339332.1:p.Arg41Pro
NM_001352406.2:c.32G>C	NP_001339335.1:p.Arg11Pro
NM_001352407.2:c.32G>C	NP_001339336.1:p.Arg11Pro
NR_029377.2:n.634G>C
NR_147978.2:n.634G>C
NR_147979.2:n.654G>C
NR_147980.2:n.530G>C
NR_147981.2:n.768G>C
NR_147982.2:n.768G>C
NR_147983.2:n.684G>C
NM_001352408.2:c.593G>C	NP_001339337.1:p.Arg198Pro