Canonical Allele Identifier: CA10289109

Gene: PPARA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46232073G>A , CM000684.2:g.46232073G>A	GRCh38
NC_000022.10:g.46627970G>A , CM000684.1:g.46627970G>A	GRCh37
NC_000022.9:g.45006634G>A	NCBI36
NG_012204.1:g.86472G>A
NG_012204.2:g.86540G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407236.6:c.993G>A MANE Select	ENSP00000385523.1:p.Leu331=
ENST00000262735.9:c.993G>A	ENSP00000262735.5:p.Leu331=
ENST00000402126.1:c.993G>A	ENSP00000385246.1:p.Leu331=
ENST00000407236.5:c.993G>A	ENSP00000385523.1:p.Leu331=
NM_001001928.2:c.993G>A	NP_001001928.1:p.Leu331=
NM_005036.4:c.993G>A	NP_005027.2:p.Leu331=
XM_005261655.2:c.993G>A	XP_005261712.1:p.Leu331=
XM_005261656.2:c.993G>A	XP_005261713.1:p.Leu331=
XM_006724269.2:c.993G>A	XP_006724332.1:p.Leu331=
XM_006724270.2:c.993G>A	XP_006724333.1:p.Leu331=
XM_011530239.1:c.993G>A	XP_011528541.1:p.Leu331=
XM_011530240.1:c.993G>A	XP_011528542.1:p.Leu331=
XM_011530241.1:c.993G>A	XP_011528543.1:p.Leu331=
XM_011530242.1:c.993G>A	XP_011528544.1:p.Leu331=
XM_011530243.1:c.993G>A	XP_011528545.1:p.Leu331=
XM_011530244.1:c.591G>A	XP_011528546.1:p.Leu197=
XM_011530245.1:c.591G>A	XP_011528547.1:p.Leu197=
XR_937869.1:n.1109G>A
XR_937870.1:n.1104G>A
NM_001001928.3:c.993G>A	NP_001001928.1:p.Leu331=
NM_001362872.1:c.993G>A	NP_001349801.1:p.Leu331=
NM_001362873.1:c.993G>A	NP_001349802.1:p.Leu331=
NM_005036.5:c.993G>A	NP_005027.2:p.Leu331=
XM_005261656.3:c.993G>A	XP_005261713.1:p.Leu331=
XM_006724270.3:c.993G>A	XP_006724333.1:p.Leu331=
XM_011530239.2:c.993G>A	XP_011528541.1:p.Leu331=
XM_011530240.2:c.993G>A	XP_011528542.1:p.Leu331=
XM_011530241.2:c.993G>A	XP_011528543.1:p.Leu331=
XM_011530242.2:c.993G>A	XP_011528544.1:p.Leu331=
XM_011530243.2:c.993G>A	XP_011528545.1:p.Leu331=
XM_011530244.2:c.591G>A	XP_011528546.1:p.Leu197=
XM_011530245.2:c.591G>A	XP_011528547.1:p.Leu197=
XM_017028839.1:c.591G>A	XP_016884328.1:p.Leu197=
XM_024452252.1:c.591G>A	XP_024308020.1:p.Leu197=
XM_024452253.1:c.384G>A	XP_024308021.1:p.Leu128=
XR_001755253.1:n.1315G>A
XR_937869.2:n.1112G>A
XR_937870.2:n.1108G>A
NM_001362872.2:c.993G>A	NP_001349801.1:p.Leu331=
NM_005036.6:c.993G>A MANE Select	NP_005027.2:p.Leu331=
NM_001001928.4:c.993G>A	NP_001001928.1:p.Leu331=
NM_001001929.3:c.993G>A	NP_001001929.1:p.Leu331=
NM_001362873.3:c.993G>A	NP_001349802.1:p.Leu331=
NM_001393941.1:c.993G>A	NP_001380870.1:p.Leu331=
NM_001393942.1:c.993G>A	NP_001380871.1:p.Leu331=
NM_001393943.1:c.993G>A	NP_001380872.1:p.Leu331=
NM_001393944.1:c.993G>A	NP_001380873.1:p.Leu331=
NM_001393945.1:c.993G>A	NP_001380874.1:p.Leu331=
NM_001393946.1:c.978G>A	NP_001380875.1:p.Leu326=
NM_001393947.1:c.509-3060G>A	NP_001380876.1:n.509-3060G>A