Canonical Allele Identifier: CA14998083

Gene: PPARA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46154203A>G , CM000684.2:g.46154203A>G	GRCh38
NC_000022.10:g.46550106A>G , CM000684.1:g.46550106A>G	GRCh37
NC_000022.9:g.44928770A>G	NCBI36
NG_012204.1:g.8608A>G
NG_012204.2:g.8670A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407236.6:c.-127+2233A>G MANE Select	ENSP00000385523.1:n.-127+2233A>G
ENST00000262735.9:c.-43+2233A>G	ENSP00000262735.5:n.-43+2233A>G
ENST00000407236.5:c.-127+2233A>G	ENSP00000385523.1:n.-127+2233A>G
ENST00000415785.5:c.-140+2233A>G	ENSP00000411677.1:n.-140+2233A>G
ENST00000420804.5:c.-43+2233A>G	ENSP00000414752.1:n.-43+2233A>G
ENST00000440343.5:c.-127+2233A>G	ENSP00000397291.1:n.-127+2233A>G
ENST00000496865.1:n.86-2027A>G
NM_001001928.2:c.-43+2233A>G	NP_001001928.1:n.-43+2233A>G
NM_005036.4:c.-127+2233A>G	NP_005027.2:n.-127+2233A>G
XM_005261655.2:c.-127+2233A>G	XP_005261712.1:n.-127+2233A>G
XM_006724269.2:c.-124+2233A>G	XP_006724332.1:n.-124+2233A>G
XM_006724270.2:c.-40+2233A>G	XP_006724333.1:n.-40+2233A>G
XM_011530239.1:c.-224+2233A>G	XP_011528541.1:n.-224+2233A>G
XM_011530240.1:c.-227+2233A>G	XP_011528542.1:n.-227+2233A>G
XM_011530241.1:c.-140+2233A>G	XP_011528543.1:n.-140+2233A>G
XM_011530244.1:c.-633+2233A>G	XP_011528546.1:n.-633+2233A>G
XM_011530245.1:c.-449+2233A>G	XP_011528547.1:n.-449+2233A>G
XR_937869.1:n.189+2233A>G
XR_937870.1:n.188+2233A>G
NM_001001928.3:c.-43+2233A>G	NP_001001928.1:n.-43+2233A>G
NM_001362872.1:c.-124+2233A>G	NP_001349801.1:n.-124+2233A>G
NM_001362873.1:c.-127+2233A>G	NP_001349802.1:n.-127+2233A>G
NM_005036.5:c.-127+2233A>G	NP_005027.2:n.-127+2233A>G
XM_006724270.3:c.-40+2233A>G	XP_006724333.1:n.-40+2233A>G
XM_011530239.2:c.-224+2233A>G	XP_011528541.1:n.-224+2233A>G
XM_011530240.2:c.-227+2233A>G	XP_011528542.1:n.-227+2233A>G
XM_011530241.2:c.-140+2233A>G	XP_011528543.1:n.-140+2233A>G
XM_011530244.2:c.-633+2233A>G	XP_011528546.1:n.-633+2233A>G
XM_011530245.2:c.-449+2233A>G	XP_011528547.1:n.-449+2233A>G
XM_017028839.1:c.-808+2233A>G	XP_016884328.1:n.-808+2233A>G
XM_024452252.1:c.-630+2233A>G	XP_024308020.1:n.-630+2233A>G
XM_024452253.1:c.-630+2233A>G	XP_024308021.1:n.-630+2233A>G
XR_001755253.1:n.192+2233A>G
XR_937869.2:n.192+2233A>G
XR_937870.2:n.192+2233A>G
NM_001362872.2:c.-124+2233A>G	NP_001349801.1:n.-124+2233A>G
NM_005036.6:c.-127+2233A>G MANE Select	NP_005027.2:n.-127+2233A>G
NM_001001928.4:c.-43+2233A>G	NP_001001928.1:n.-43+2233A>G
NM_001362873.3:c.-127+2233A>G	NP_001349802.1:n.-127+2233A>G
NM_001393941.1:c.-40+2233A>G	NP_001380870.1:n.-40+2233A>G
NM_001393942.1:c.-140+2233A>G	NP_001380871.1:n.-140+2233A>G
NM_001393943.1:c.-124+2233A>G	NP_001380872.1:n.-124+2233A>G
NM_001393944.1:c.-40+2233A>G	NP_001380873.1:n.-40+2233A>G
NM_001393945.1:c.-43+2233A>G	NP_001380874.1:n.-43+2233A>G
NM_001393946.1:c.-124+2233A>G	NP_001380875.1:n.-124+2233A>G
NM_001393947.1:c.-43+2233A>G	NP_001380876.1:n.-43+2233A>G