Canonical Allele Identifier: CA2351374340
Gene: NDUFAF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13801528A= , CM000682.2:g.13801528A= GRCh38
NC_000020.10:g.13782174A= , CM000682.1:g.13782174A= GRCh37
NC_000020.9:g.13730174A= NCBI36
NG_015811.1:g.21503A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378106.10:c.562A= MANE Select ENSP00000367346.5:p.Met188=
ENST00000378081.9:c.562A= ENSP00000437325.1:p.Met188=
ENST00000378106.9:c.562A= ENSP00000367346.5:p.Met188=
ENST00000463598.1:c.478A= ENSP00000420497.1:p.Met160=
ENST00000464269.5:n.235A=
ENST00000475968.5:n.439A=
ENST00000476536.5:n.522A=
ENST00000477732.5:n.502+3028A=
ENST00000479716.5:n.83A=
ENST00000481249.5:n.439A=
ENST00000485738.5:n.539A=
NM_001039375.2:c.478A= NP_001034464.1:p.Met160=
NM_024120.4:c.562A= NP_077025.2:p.Met188=
NR_029377.1:n.605A=
XM_006723620.2:c.562A= XP_006723683.1:p.Met188=
XM_006723622.2:c.91A= XP_006723685.1:p.Met31=
XM_006723623.1:c.91A= XP_006723686.1:p.Met31=
XM_006723624.1:c.91A= XP_006723687.1:p.Met31=
XM_011529341.1:c.562A= XP_011527643.1:p.Met188=
XM_011529342.1:c.562A= XP_011527644.1:p.Met188=
XM_011529343.1:c.562A= XP_011527645.1:p.Met188=
XM_011529344.1:c.193A= XP_011527646.1:p.Met65=
XR_430269.2:n.582A=
XR_937140.1:n.582A=
NM_001352403.1:c.91A= NP_001339332.1:p.Met31=
NM_001352406.1:c.1A= NP_001339335.1:p.Met1=
NM_001352407.1:c.1A= NP_001339336.1:p.Met1=
NM_001352408.1:c.562A= NP_001339337.1:p.Met188=
NR_147978.1:n.605A=
NR_147979.1:n.625A=
NR_147980.1:n.501A=
NR_147981.1:n.739A=
NR_147982.1:n.739A=
NR_147983.1:n.655A=
XM_006723624.2:c.91A= XP_006723687.1:p.Met31=
XM_011529342.2:c.562A= XP_011527644.1:p.Met188=
XM_024451999.1:c.91A= XP_024307767.1:p.Met31=
XR_001754396.1:n.521A=
XR_430269.3:n.582A=
XR_937140.2:n.582A=
NM_024120.5:c.562A= MANE Select NP_077025.2:p.Met188=
NM_001039375.3:c.478A= NP_001034464.1:p.Met160=
NM_001352403.2:c.91A= NP_001339332.1:p.Met31=
NM_001352406.2:c.1A= NP_001339335.1:p.Met1=
NM_001352407.2:c.1A= NP_001339336.1:p.Met1=
NR_029377.2:n.603A=
NR_147978.2:n.603A=
NR_147979.2:n.623A=
NR_147980.2:n.499A=
NR_147981.2:n.737A=
NR_147982.2:n.737A=
NR_147983.2:n.653A=
NM_001352408.2:c.562A= NP_001339337.1:p.Met188=