Canonical Allele Identifier: CA14978070
Gene: PPARA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46166284T>C , CM000684.2:g.46166284T>C GRCh38
NC_000022.10:g.46562183T>C , CM000684.1:g.46562183T>C GRCh37
NC_000022.9:g.44940847T>C NCBI36
NG_012204.1:g.20685T>C
NG_012204.2:g.20751T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000407236.6:c.-126-10469T>C MANE Select ENSP00000385523.1:n.-126-10469T>C
ENST00000262735.9:c.-43+14314T>C ENSP00000262735.5:n.-43+14314T>C
ENST00000407236.5:c.-126-10469T>C ENSP00000385523.1:n.-126-10469T>C
ENST00000415785.5:c.-140+14314T>C ENSP00000411677.1:n.-140+14314T>C
ENST00000420804.5:c.-43+14314T>C ENSP00000414752.1:n.-43+14314T>C
ENST00000440343.5:c.-126-10469T>C ENSP00000397291.1:n.-126-10469T>C
NM_001001928.2:c.-43+14314T>C NP_001001928.1:n.-43+14314T>C
NM_005036.4:c.-126-10469T>C NP_005027.2:n.-126-10469T>C
XM_005261655.2:c.-126-10469T>C XP_005261712.1:n.-126-10469T>C
XM_006724269.2:c.-123-10469T>C XP_006724332.1:n.-123-10469T>C
XM_006724270.2:c.-40+14314T>C XP_006724333.1:n.-40+14314T>C
XM_011530239.1:c.-223-10469T>C XP_011528541.1:n.-223-10469T>C
XM_011530240.1:c.-226-10469T>C XP_011528542.1:n.-226-10469T>C
XM_011530241.1:c.-140+14314T>C XP_011528543.1:n.-140+14314T>C
XM_011530244.1:c.-632-10469T>C XP_011528546.1:n.-632-10469T>C
XM_011530245.1:c.-449+14314T>C XP_011528547.1:n.-449+14314T>C
XR_937869.1:n.190-10469T>C
XR_937870.1:n.189-10469T>C
XR_938315.1:n.249-4962A>G
NM_001001928.3:c.-43+14314T>C NP_001001928.1:n.-43+14314T>C
NM_001362872.1:c.-123-10469T>C NP_001349801.1:n.-123-10469T>C
NM_001362873.1:c.-126-10469T>C NP_001349802.1:n.-126-10469T>C
NM_005036.5:c.-126-10469T>C NP_005027.2:n.-126-10469T>C
XM_006724270.3:c.-40+14314T>C XP_006724333.1:n.-40+14314T>C
XM_011530239.2:c.-223-10469T>C XP_011528541.1:n.-223-10469T>C
XM_011530240.2:c.-226-10469T>C XP_011528542.1:n.-226-10469T>C
XM_011530241.2:c.-140+14314T>C XP_011528543.1:n.-140+14314T>C
XM_011530244.2:c.-632-10469T>C XP_011528546.1:n.-632-10469T>C
XM_011530245.2:c.-449+14314T>C XP_011528547.1:n.-449+14314T>C
XM_017028839.1:c.-807-10469T>C XP_016884328.1:n.-807-10469T>C
XM_024452252.1:c.-629-10469T>C XP_024308020.1:n.-629-10469T>C
XM_024452253.1:c.-629-10469T>C XP_024308021.1:n.-629-10469T>C
XR_001755253.1:n.193-10469T>C
XR_937869.2:n.193-10469T>C
XR_937870.2:n.193-10469T>C
XR_938315.2:n.255-4962A>G
NM_001362872.2:c.-123-10469T>C NP_001349801.1:n.-123-10469T>C
NM_005036.6:c.-126-10469T>C MANE Select NP_005027.2:n.-126-10469T>C
NM_001001928.4:c.-43+14314T>C NP_001001928.1:n.-43+14314T>C
NM_001362873.3:c.-126-10469T>C NP_001349802.1:n.-126-10469T>C
NM_001393941.1:c.-40+14314T>C NP_001380870.1:n.-40+14314T>C
NM_001393942.1:c.-140+14314T>C NP_001380871.1:n.-140+14314T>C
NM_001393943.1:c.-123-10469T>C NP_001380872.1:n.-123-10469T>C
NM_001393944.1:c.-40+14314T>C NP_001380873.1:n.-40+14314T>C
NM_001393945.1:c.-43+14314T>C NP_001380874.1:n.-43+14314T>C
NM_001393946.1:c.-123-10469T>C NP_001380875.1:n.-123-10469T>C
NM_001393947.1:c.-43+14314T>C NP_001380876.1:n.-43+14314T>C
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