Canonical Allele Identifier: CA408271249

Gene: NDUFAF5

Linked Data

• ClinVar Variation Id: 1461718
• ClinVar RCV Id: RCV001965998
• dbSNP Id: rs2147553797
• MyVariant Identifiers: chr20:g.13782325C>T (hg19) ; chr20:g.13801679C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801679C>T , CM000682.2:g.13801679C>T	GRCh38
NC_000020.10:g.13782325C>T , CM000682.1:g.13782325C>T	GRCh37
NC_000020.9:g.13730325C>T	NCBI36
NG_015811.1:g.21654C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378106.10:c.713C>T MANE Select	ENSP00000367346.5:p.Thr238Ile
ENST00000378081.9:c.713C>T	ENSP00000437325.1:p.Thr238Ile
ENST00000378106.9:c.713C>T	ENSP00000367346.5:p.Thr238Ile
ENST00000463598.1:c.629C>T	ENSP00000420497.1:p.Thr210Ile
ENST00000464269.5:n.386C>T
ENST00000475968.5:n.590C>T
ENST00000476124.1:n.112C>T
ENST00000476536.5:n.673C>T
ENST00000477732.5:n.502+3179C>T
ENST00000479716.5:n.234C>T
ENST00000481249.5:n.590C>T
ENST00000485738.5:n.690C>T
ENST00000487478.5:n.137C>T
NM_001039375.2:c.629C>T	NP_001034464.1:p.Thr210Ile
NM_024120.4:c.713C>T	NP_077025.2:p.Thr238Ile
NR_029377.1:n.756C>T
XM_006723620.2:c.713C>T	XP_006723683.1:p.Thr238Ile
XM_006723622.2:c.242C>T	XP_006723685.1:p.Thr81Ile
XM_006723623.1:c.242C>T	XP_006723686.1:p.Thr81Ile
XM_006723624.1:c.242C>T	XP_006723687.1:p.Thr81Ile
XM_011529341.1:c.713C>T	XP_011527643.1:p.Thr238Ile
XM_011529342.1:c.713C>T	XP_011527644.1:p.Thr238Ile
XM_011529343.1:c.713C>T	XP_011527645.1:p.Thr238Ile
XM_011529344.1:c.344C>T	XP_011527646.1:p.Thr115Ile
XR_430269.2:n.733C>T
XR_937140.1:n.733C>T
NM_001352403.1:c.242C>T	NP_001339332.1:p.Thr81Ile
NM_001352406.1:c.152C>T	NP_001339335.1:p.Thr51Ile
NM_001352407.1:c.152C>T	NP_001339336.1:p.Thr51Ile
NM_001352408.1:c.713C>T	NP_001339337.1:p.Thr238Ile
NR_147978.1:n.756C>T
NR_147979.1:n.776C>T
NR_147980.1:n.652C>T
NR_147981.1:n.890C>T
NR_147982.1:n.890C>T
NR_147983.1:n.806C>T
XM_006723624.2:c.242C>T	XP_006723687.1:p.Thr81Ile
XM_011529342.2:c.713C>T	XP_011527644.1:p.Thr238Ile
XM_024451999.1:c.242C>T	XP_024307767.1:p.Thr81Ile
XR_001754396.1:n.672C>T
XR_430269.3:n.733C>T
XR_937140.2:n.733C>T
NM_024120.5:c.713C>T MANE Select	NP_077025.2:p.Thr238Ile
NM_001039375.3:c.629C>T	NP_001034464.1:p.Thr210Ile
NM_001352403.2:c.242C>T	NP_001339332.1:p.Thr81Ile
NM_001352406.2:c.152C>T	NP_001339335.1:p.Thr51Ile
NM_001352407.2:c.152C>T	NP_001339336.1:p.Thr51Ile
NR_029377.2:n.754C>T
NR_147978.2:n.754C>T
NR_147979.2:n.774C>T
NR_147980.2:n.650C>T
NR_147981.2:n.888C>T
NR_147982.2:n.888C>T
NR_147983.2:n.804C>T
NM_001352408.2:c.713C>T	NP_001339337.1:p.Thr238Ile