Canonical Allele Identifier: CA408271229

Gene: NDUFAF5

Linked Data

• COSMIC: COSM3740013
• MyVariant Identifiers: chr20:g.13782322T>C (hg19) ; chr20:g.13801676T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801676T>C , CM000682.2:g.13801676T>C	GRCh38
NC_000020.10:g.13782322T>C , CM000682.1:g.13782322T>C	GRCh37
NC_000020.9:g.13730322T>C	NCBI36
NG_015811.1:g.21651T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.710T>C MANE Select	ENSP00000367346.5:p.Leu237Pro
ENST00000378081.9:c.710T>C	ENSP00000437325.1:p.Leu237Pro
ENST00000378106.9:c.710T>C	ENSP00000367346.5:p.Leu237Pro
ENST00000463598.1:c.626T>C	ENSP00000420497.1:p.Leu209Pro
ENST00000464269.5:n.383T>C
ENST00000475968.5:n.587T>C
ENST00000476124.1:n.109T>C
ENST00000476536.5:n.670T>C
ENST00000477732.5:n.502+3176T>C
ENST00000479716.5:n.231T>C
ENST00000481249.5:n.587T>C
ENST00000485738.5:n.687T>C
ENST00000487478.5:n.134T>C
NM_001039375.2:c.626T>C	NP_001034464.1:p.Leu209Pro
NM_024120.4:c.710T>C	NP_077025.2:p.Leu237Pro
NR_029377.1:n.753T>C
XM_006723620.2:c.710T>C	XP_006723683.1:p.Leu237Pro
XM_006723622.2:c.239T>C	XP_006723685.1:p.Leu80Pro
XM_006723623.1:c.239T>C	XP_006723686.1:p.Leu80Pro
XM_006723624.1:c.239T>C	XP_006723687.1:p.Leu80Pro
XM_011529341.1:c.710T>C	XP_011527643.1:p.Leu237Pro
XM_011529342.1:c.710T>C	XP_011527644.1:p.Leu237Pro
XM_011529343.1:c.710T>C	XP_011527645.1:p.Leu237Pro
XM_011529344.1:c.341T>C	XP_011527646.1:p.Leu114Pro
XR_430269.2:n.730T>C
XR_937140.1:n.730T>C
NM_001352403.1:c.239T>C	NP_001339332.1:p.Leu80Pro
NM_001352406.1:c.149T>C	NP_001339335.1:p.Leu50Pro
NM_001352407.1:c.149T>C	NP_001339336.1:p.Leu50Pro
NM_001352408.1:c.710T>C	NP_001339337.1:p.Leu237Pro
NR_147978.1:n.753T>C
NR_147979.1:n.773T>C
NR_147980.1:n.649T>C
NR_147981.1:n.887T>C
NR_147982.1:n.887T>C
NR_147983.1:n.803T>C
XM_006723624.2:c.239T>C	XP_006723687.1:p.Leu80Pro
XM_011529342.2:c.710T>C	XP_011527644.1:p.Leu237Pro
XM_024451999.1:c.239T>C	XP_024307767.1:p.Leu80Pro
XR_001754396.1:n.669T>C
XR_430269.3:n.730T>C
XR_937140.2:n.730T>C
NM_024120.5:c.710T>C MANE Select	NP_077025.2:p.Leu237Pro
NM_001039375.3:c.626T>C	NP_001034464.1:p.Leu209Pro
NM_001352403.2:c.239T>C	NP_001339332.1:p.Leu80Pro
NM_001352406.2:c.149T>C	NP_001339335.1:p.Leu50Pro
NM_001352407.2:c.149T>C	NP_001339336.1:p.Leu50Pro
NR_029377.2:n.751T>C
NR_147978.2:n.751T>C
NR_147979.2:n.771T>C
NR_147980.2:n.647T>C
NR_147981.2:n.885T>C
NR_147982.2:n.885T>C
NR_147983.2:n.801T>C
NM_001352408.2:c.710T>C	NP_001339337.1:p.Leu237Pro