Canonical Allele Identifier: CA14944293
Gene: PPARA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46173274G>A , CM000684.2:g.46173274G>A GRCh38
NC_000022.10:g.46569171G>A , CM000684.1:g.46569171G>A GRCh37
NC_000022.9:g.44947835G>A NCBI36
NG_012204.1:g.27673G>A
NG_012204.2:g.27741G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407236.6:c.-126-3479G>A MANE Select ENSP00000385523.1:n.-126-3479G>A
ENST00000262735.9:c.-43+21304G>A ENSP00000262735.5:n.-43+21304G>A
ENST00000407236.5:c.-126-3479G>A ENSP00000385523.1:n.-126-3479G>A
ENST00000415785.5:c.-139-15449G>A ENSP00000411677.1:n.-139-15449G>A
ENST00000420804.5:c.-43+21304G>A ENSP00000414752.1:n.-43+21304G>A
ENST00000440343.5:c.-126-3479G>A ENSP00000397291.1:n.-126-3479G>A
ENST00000481567.5:n.161+1782G>A
ENST00000484619.1:n.209+1782G>A
NM_001001928.2:c.-43+21304G>A NP_001001928.1:n.-43+21304G>A
NM_005036.4:c.-126-3479G>A NP_005027.2:n.-126-3479G>A
XM_005261655.2:c.-126-3479G>A XP_005261712.1:n.-126-3479G>A
XM_005261656.2:c.-380+1782G>A XP_005261713.1:n.-380+1782G>A
XM_006724269.2:c.-123-3479G>A XP_006724332.1:n.-123-3479G>A
XM_006724270.2:c.-40+21304G>A XP_006724333.1:n.-40+21304G>A
XM_011530239.1:c.-223-3479G>A XP_011528541.1:n.-223-3479G>A
XM_011530240.1:c.-226-3479G>A XP_011528542.1:n.-226-3479G>A
XM_011530241.1:c.-139-15449G>A XP_011528543.1:n.-139-15449G>A
XM_011530243.1:c.-43+1782G>A XP_011528545.1:n.-43+1782G>A
XM_011530244.1:c.-632-3479G>A XP_011528546.1:n.-632-3479G>A
XM_011530245.1:c.-449+21304G>A XP_011528547.1:n.-449+21304G>A
XR_937869.1:n.190-3479G>A
XR_937870.1:n.189-3479G>A
NM_001001928.3:c.-43+21304G>A NP_001001928.1:n.-43+21304G>A
NM_001362872.1:c.-123-3479G>A NP_001349801.1:n.-123-3479G>A
NM_001362873.1:c.-126-3479G>A NP_001349802.1:n.-126-3479G>A
NM_005036.5:c.-126-3479G>A NP_005027.2:n.-126-3479G>A
XM_005261656.3:c.-380+1782G>A XP_005261713.1:n.-380+1782G>A
XM_006724270.3:c.-40+21304G>A XP_006724333.1:n.-40+21304G>A
XM_011530239.2:c.-223-3479G>A XP_011528541.1:n.-223-3479G>A
XM_011530240.2:c.-226-3479G>A XP_011528542.1:n.-226-3479G>A
XM_011530241.2:c.-139-15449G>A XP_011528543.1:n.-139-15449G>A
XM_011530243.2:c.-43+1782G>A XP_011528545.1:n.-43+1782G>A
XM_011530244.2:c.-632-3479G>A XP_011528546.1:n.-632-3479G>A
XM_011530245.2:c.-449+21304G>A XP_011528547.1:n.-449+21304G>A
XM_017028839.1:c.-807-3479G>A XP_016884328.1:n.-807-3479G>A
XM_024452252.1:c.-629-3479G>A XP_024308020.1:n.-629-3479G>A
XM_024452253.1:c.-629-3479G>A XP_024308021.1:n.-629-3479G>A
XR_001755253.1:n.193-3479G>A
XR_937869.2:n.193-3479G>A
XR_937870.2:n.193-3479G>A
NM_001362872.2:c.-123-3479G>A NP_001349801.1:n.-123-3479G>A
NM_005036.6:c.-126-3479G>A MANE Select NP_005027.2:n.-126-3479G>A
NM_001001928.4:c.-43+21304G>A NP_001001928.1:n.-43+21304G>A
NM_001001929.3:c.-43+1782G>A NP_001001929.1:n.-43+1782G>A
NM_001362873.3:c.-126-3479G>A NP_001349802.1:n.-126-3479G>A
NM_001393941.1:c.-40+21304G>A NP_001380870.1:n.-40+21304G>A
NM_001393942.1:c.-139-15449G>A NP_001380871.1:n.-139-15449G>A
NM_001393943.1:c.-123-3479G>A NP_001380872.1:n.-123-3479G>A
NM_001393944.1:c.-40+21304G>A NP_001380873.1:n.-40+21304G>A
NM_001393945.1:c.-43+21304G>A NP_001380874.1:n.-43+21304G>A
NM_001393946.1:c.-123-3479G>A NP_001380875.1:n.-123-3479G>A
NM_001393947.1:c.-43+21304G>A NP_001380876.1:n.-43+21304G>A
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