Canonical Allele Identifier: CA351619398
Gene: PPARG HGNC NCBI

Linked Data

dbSNP Id: rs2051076789
gnomAD v3: 3-12416839-G-A
gnomAD v4: 3-12416839-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12416839G>A , CM000665.2:g.12416839G>A GRCh38
NC_000003.11:g.12458338G>A , CM000665.1:g.12458338G>A GRCh37
NC_000003.10:g.12433338G>A NCBI36
NG_011749.1:g.133990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000681966.1:c.*119G>A ENSP00000507572.1:n.*119G>A
ENST00000681982.1:c.865G>A ENSP00000508065.1:p.Glu289Lys
ENST00000682125.1:n.910G>A
ENST00000682446.1:c.865G>A ENSP00000506813.1:p.Glu289Lys
ENST00000682494.1:n.3765G>A
ENST00000682604.1:n.1108G>A
ENST00000683586.1:c.865G>A ENSP00000507893.1:p.Glu289Lys
ENST00000683699.1:c.819+10758G>A ENSP00000507823.1:n.819+10758G>A
ENST00000683700.1:c.718G>A ENSP00000508248.1:p.Glu240Lys
ENST00000684065.1:c.*466+10758G>A ENSP00000508347.1:n.*466+10758G>A
ENST00000684094.1:n.1507G>A
ENST00000309576.11:c.865G>A ENSP00000312472.7:p.Glu289Lys
ENST00000396999.3:c.*453G>A ENSP00000380195.3:n.*453G>A
ENST00000397000.6:c.729+10758G>A ENSP00000380196.2:n.729+10758G>A
ENST00000397010.7:c.865G>A ENSP00000380205.3:p.Glu289Lys
ENST00000397015.7:c.865G>A ENSP00000380210.3:p.Glu289Lys
ENST00000397026.7:c.865G>A ENSP00000380221.3:p.Glu289Lys
ENST00000643197.2:c.865G>A ENSP00000495840.2:p.Glu289Lys
ENST00000643888.2:c.865G>A ENSP00000494934.2:p.Glu289Lys
ENST00000644622.2:c.865G>A ENSP00000494873.2:p.Glu289Lys
ENST00000651735.1:c.865G>A MANE Select ENSP00000498313.1:p.Glu289Lys
ENST00000652098.1:c.319G>A ENSP00000498300.1:p.Glu107Lys
ENST00000652431.1:c.553G>A ENSP00000498717.1:p.Glu185Lys
ENST00000652522.1:c.865G>A ENSP00000498500.1:p.Glu289Lys
ENST00000287820.10:c.955G>A ENSP00000287820.6:p.Glu319Lys
ENST00000309576.10:c.871G>A ENSP00000312472.6:p.Glu291Lys
ENST00000396999.2:c.1014G>A ENSP00000380195.2:n.1014G>A
ENST00000397000.5:c.735+10758G>A ENSP00000380196.1:n.735+10758G>A
ENST00000397010.6:c.871G>A ENSP00000380205.2:p.Glu291Lys
ENST00000397012.6:c.871G>A ENSP00000380207.2:p.Glu291Lys
ENST00000397015.6:c.871G>A ENSP00000380210.2:p.Glu291Lys
ENST00000397023.5:c.*1093G>A ENSP00000380218.1:n.*1093G>A
ENST00000397026.6:c.889G>A ENSP00000380221.2:p.Glu297Lys
NM_005037.5:c.871G>A NP_005028.4:p.Glu291Lys
NM_015869.4:c.955G>A NP_056953.2:p.Glu319Lys
NM_138711.3:c.871G>A NP_619725.2:p.Glu291Lys
NM_138712.3:c.871G>A NP_619726.2:p.Glu291Lys
XM_011533840.1:c.871G>A XP_011532142.1:p.Glu291Lys
XM_011533841.1:c.871G>A XP_011532143.1:p.Glu291Lys
XM_011533842.1:c.955G>A XP_011532144.1:p.Glu319Lys
XM_011533843.1:c.819+10758G>A XP_011532145.1:n.819+10758G>A
XM_011533844.1:c.735+10758G>A XP_011532146.1:n.735+10758G>A
NM_001330615.1:c.735+10758G>A NP_001317544.1:n.735+10758G>A
NM_001354666.1:c.871G>A NP_001341595.1:p.Glu291Lys
NM_001354667.1:c.871G>A NP_001341596.1:p.Glu291Lys
NM_001354669.1:c.238G>A NP_001341598.1:p.Glu80Lys
XM_011533842.2:c.955G>A XP_011532144.1:p.Glu319Lys
XM_011533843.2:c.819+10758G>A XP_011532145.1:n.819+10758G>A
XM_024453604.1:c.871G>A XP_024309372.1:p.Glu291Lys
XM_024453605.1:c.871G>A XP_024309373.1:p.Glu291Lys
XM_024453606.1:c.871G>A XP_024309374.1:p.Glu291Lys
NM_001330615.2:c.735+10758G>A NP_001317544.1:n.735+10758G>A
NM_001354666.2:c.871G>A NP_001341595.1:p.Glu291Lys
NM_001354667.2:c.871G>A NP_001341596.1:p.Glu291Lys
NM_001354669.2:c.238G>A NP_001341598.1:p.Glu80Lys
NM_001374261.1:c.735+10758G>A NP_001361190.1:n.735+10758G>A
NM_001374262.1:c.735+10758G>A NP_001361191.1:n.735+10758G>A
NM_001374263.1:c.871G>A NP_001361192.1:p.Glu291Lys
NM_001374264.1:c.871G>A NP_001361193.1:p.Glu291Lys
NM_001374265.1:c.819+10758G>A NP_001361194.1:n.819+10758G>A
NM_001374266.1:c.653+10840G>A NP_001361195.1:n.653+10840G>A
NM_005037.6:c.871G>A NP_005028.4:p.Glu291Lys
NM_015869.5:c.955G>A NP_056953.2:p.Glu319Lys
NM_138711.4:c.871G>A NP_619725.2:p.Glu291Lys
NM_138712.4:c.871G>A NP_619726.2:p.Glu291Lys
NM_001330615.4:c.729+10758G>A NP_001317544.2:n.729+10758G>A
NM_001354666.3:c.865G>A NP_001341595.2:p.Glu289Lys
NM_001354667.3:c.865G>A NP_001341596.2:p.Glu289Lys
NM_001374261.3:c.729+10758G>A NP_001361190.2:n.729+10758G>A
NM_001374262.3:c.729+10758G>A NP_001361191.2:n.729+10758G>A
NM_001374263.2:c.865G>A NP_001361192.2:p.Glu289Lys
NM_001374264.2:c.865G>A NP_001361193.2:p.Glu289Lys
NM_005037.7:c.865G>A NP_005028.5:p.Glu289Lys
NM_138711.6:c.865G>A MANE Select NP_619725.3:p.Glu289Lys
NM_138712.5:c.865G>A NP_619726.3:p.Glu289Lys