Canonical Allele Identifier: CA509676227

Gene: NDUFAF5

Linked Data

• dbSNP Id: rs1170894267
• MyVariant Identifiers: chr20:g.13782308T>C (hg19) ; chr20:g.13801662T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13801662T>C , CM000682.2:g.13801662T>C	GRCh38
NC_000020.10:g.13782308T>C , CM000682.1:g.13782308T>C	GRCh37
NC_000020.9:g.13730308T>C	NCBI36
NG_015811.1:g.21637T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378106.10:c.696T>C MANE Select	ENSP00000367346.5:p.Ala232=
ENST00000378081.9:c.696T>C	ENSP00000437325.1:p.Ala232=
ENST00000378106.9:c.696T>C	ENSP00000367346.5:p.Ala232=
ENST00000463598.1:c.612T>C	ENSP00000420497.1:p.Ala204=
ENST00000464269.5:n.369T>C
ENST00000475968.5:n.573T>C
ENST00000476124.1:n.95T>C
ENST00000476536.5:n.656T>C
ENST00000477732.5:n.502+3162T>C
ENST00000479716.5:n.217T>C
ENST00000481249.5:n.573T>C
ENST00000485738.5:n.673T>C
ENST00000487478.5:n.120T>C
NM_001039375.2:c.612T>C	NP_001034464.1:p.Ala204=
NM_024120.4:c.696T>C	NP_077025.2:p.Ala232=
NR_029377.1:n.739T>C
XM_006723620.2:c.696T>C	XP_006723683.1:p.Ala232=
XM_006723622.2:c.225T>C	XP_006723685.1:p.Ala75=
XM_006723623.1:c.225T>C	XP_006723686.1:p.Ala75=
XM_006723624.1:c.225T>C	XP_006723687.1:p.Ala75=
XM_011529341.1:c.696T>C	XP_011527643.1:p.Ala232=
XM_011529342.1:c.696T>C	XP_011527644.1:p.Ala232=
XM_011529343.1:c.696T>C	XP_011527645.1:p.Ala232=
XM_011529344.1:c.327T>C	XP_011527646.1:p.Ala109=
XR_430269.2:n.716T>C
XR_937140.1:n.716T>C
NM_001352403.1:c.225T>C	NP_001339332.1:p.Ala75=
NM_001352406.1:c.135T>C	NP_001339335.1:p.Ala45=
NM_001352407.1:c.135T>C	NP_001339336.1:p.Ala45=
NM_001352408.1:c.696T>C	NP_001339337.1:p.Ala232=
NR_147978.1:n.739T>C
NR_147979.1:n.759T>C
NR_147980.1:n.635T>C
NR_147981.1:n.873T>C
NR_147982.1:n.873T>C
NR_147983.1:n.789T>C
XM_006723624.2:c.225T>C	XP_006723687.1:p.Ala75=
XM_011529342.2:c.696T>C	XP_011527644.1:p.Ala232=
XM_024451999.1:c.225T>C	XP_024307767.1:p.Ala75=
XR_001754396.1:n.655T>C
XR_430269.3:n.716T>C
XR_937140.2:n.716T>C
NM_024120.5:c.696T>C MANE Select	NP_077025.2:p.Ala232=
NM_001039375.3:c.612T>C	NP_001034464.1:p.Ala204=
NM_001352403.2:c.225T>C	NP_001339332.1:p.Ala75=
NM_001352406.2:c.135T>C	NP_001339335.1:p.Ala45=
NM_001352407.2:c.135T>C	NP_001339336.1:p.Ala45=
NR_029377.2:n.737T>C
NR_147978.2:n.737T>C
NR_147979.2:n.757T>C
NR_147980.2:n.633T>C
NR_147981.2:n.871T>C
NR_147982.2:n.871T>C
NR_147983.2:n.787T>C
NM_001352408.2:c.696T>C	NP_001339337.1:p.Ala232=