Canonical Allele Identifier: CA2755254474
Gene: PPARG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12416768_12416773del , CM000665.2:g.12416768_12416773del GRCh38
NC_000003.11:g.12458267_12458272del , CM000665.1:g.12458267_12458272del GRCh37
NC_000003.10:g.12433267_12433272del NCBI36
NG_011749.1:g.133919_133924del

Transcript Alleles

HGVS Amino-acid Change
ENST00000681966.1:c.*48_*53del ENSP00000507572.1:n.*48_*53del
ENST00000681982.1:c.794_799del ENSP00000508065.1:p.Ile265_Pro267delinsThr
ENST00000682125.1:n.839_844del
ENST00000682446.1:c.794_799del ENSP00000506813.1:p.Ile265_Pro267delinsThr
ENST00000682494.1:n.3694_3699del
ENST00000682604.1:n.1037_1042del
ENST00000683586.1:c.794_799del ENSP00000507893.1:p.Ile265_Pro267delinsThr
ENST00000683699.1:c.819+10687_819+10692del ENSP00000507823.1:n.819+10687_819+10692del
ENST00000683700.1:c.647_652del ENSP00000508248.1:p.Ile216_Pro218delinsThr
ENST00000684065.1:c.*466+10687_*466+10692del ENSP00000508347.1:n.*466+10687_*466+10692del
ENST00000684094.1:n.1436_1441del
ENST00000309576.11:c.794_799del ENSP00000312472.7:p.Ile265_Pro267delinsThr
ENST00000396999.3:c.*382_*387del ENSP00000380195.3:n.*382_*387del
ENST00000397000.6:c.729+10687_729+10692del ENSP00000380196.2:n.729+10687_729+10692del
ENST00000397010.7:c.794_799del ENSP00000380205.3:p.Ile265_Pro267delinsThr
ENST00000397015.7:c.794_799del ENSP00000380210.3:p.Ile265_Pro267delinsThr
ENST00000397026.7:c.794_799del ENSP00000380221.3:p.Ile265_Pro267delinsThr
ENST00000643197.2:c.794_799del ENSP00000495840.2:p.Ile265_Pro267delinsThr
ENST00000643888.2:c.794_799del ENSP00000494934.2:p.Ile265_Pro267delinsThr
ENST00000644622.2:c.794_799del ENSP00000494873.2:p.Ile265_Pro267delinsThr
ENST00000651735.1:c.794_799del MANE Select ENSP00000498313.1:p.Ile265_Pro267delinsThr
ENST00000652098.1:c.248_253del ENSP00000498300.1:p.Ile83_Pro85delinsThr
ENST00000652431.1:c.482_487del ENSP00000498717.1:p.Ile161_Pro163delinsThr
ENST00000652522.1:c.794_799del ENSP00000498500.1:p.Ile265_Pro267delinsThr
ENST00000287820.10:c.884_889del ENSP00000287820.6:p.Ile295_Pro297delinsThr
ENST00000309576.10:c.800_805del ENSP00000312472.6:p.Ile267_Pro269delinsThr
ENST00000396999.2:c.943_948del ENSP00000380195.2:n.943_948del
ENST00000397000.5:c.735+10687_735+10692del ENSP00000380196.1:n.735+10687_735+10692del
ENST00000397010.6:c.800_805del ENSP00000380205.2:p.Ile267_Pro269delinsThr
ENST00000397012.6:c.800_805del ENSP00000380207.2:p.Ile267_Pro269delinsThr
ENST00000397015.6:c.800_805del ENSP00000380210.2:p.Ile267_Pro269delinsThr
ENST00000397023.5:c.*1022_*1027del ENSP00000380218.1:n.*1022_*1027del
ENST00000397026.6:c.818_823del ENSP00000380221.2:p.Ile273_Pro275delinsThr
NM_005037.5:c.800_805del NP_005028.4:p.Ile267_Pro269delinsThr
NM_015869.4:c.884_889del NP_056953.2:p.Ile295_Pro297delinsThr
NM_138711.3:c.800_805del NP_619725.2:p.Ile267_Pro269delinsThr
NM_138712.3:c.800_805del NP_619726.2:p.Ile267_Pro269delinsThr
XM_011533840.1:c.800_805del XP_011532142.1:p.Ile267_Pro269delinsThr
XM_011533841.1:c.800_805del XP_011532143.1:p.Ile267_Pro269delinsThr
XM_011533842.1:c.884_889del XP_011532144.1:p.Ile295_Pro297delinsThr
XM_011533843.1:c.819+10687_819+10692del XP_011532145.1:n.819+10687_819+10692del
XM_011533844.1:c.735+10687_735+10692del XP_011532146.1:n.735+10687_735+10692del
NM_001330615.1:c.735+10687_735+10692del NP_001317544.1:n.735+10687_735+10692del
NM_001354666.1:c.800_805del NP_001341595.1:p.Ile267_Pro269delinsThr
NM_001354667.1:c.800_805del NP_001341596.1:p.Ile267_Pro269delinsThr
NM_001354669.1:c.167_172del NP_001341598.1:p.Ile56_Pro58delinsThr
XM_011533842.2:c.884_889del XP_011532144.1:p.Ile295_Pro297delinsThr
XM_011533843.2:c.819+10687_819+10692del XP_011532145.1:n.819+10687_819+10692del
XM_024453604.1:c.800_805del XP_024309372.1:p.Ile267_Pro269delinsThr
XM_024453605.1:c.800_805del XP_024309373.1:p.Ile267_Pro269delinsThr
XM_024453606.1:c.800_805del XP_024309374.1:p.Ile267_Pro269delinsThr
NM_001330615.2:c.735+10687_735+10692del NP_001317544.1:n.735+10687_735+10692del
NM_001354666.2:c.800_805del NP_001341595.1:p.Ile267_Pro269delinsThr
NM_001354667.2:c.800_805del NP_001341596.1:p.Ile267_Pro269delinsThr
NM_001354669.2:c.167_172del NP_001341598.1:p.Ile56_Pro58delinsThr
NM_001374261.1:c.735+10687_735+10692del NP_001361190.1:n.735+10687_735+10692del
NM_001374262.1:c.735+10687_735+10692del NP_001361191.1:n.735+10687_735+10692del
NM_001374263.1:c.800_805del NP_001361192.1:p.Ile267_Pro269delinsThr
NM_001374264.1:c.800_805del NP_001361193.1:p.Ile267_Pro269delinsThr
NM_001374265.1:c.819+10687_819+10692del NP_001361194.1:n.819+10687_819+10692del
NM_001374266.1:c.653+10769_653+10774del NP_001361195.1:n.653+10769_653+10774del
NM_005037.6:c.800_805del NP_005028.4:p.Ile267_Pro269delinsThr
NM_015869.5:c.884_889del NP_056953.2:p.Ile295_Pro297delinsThr
NM_138711.4:c.800_805del NP_619725.2:p.Ile267_Pro269delinsThr
NM_138712.4:c.800_805del NP_619726.2:p.Ile267_Pro269delinsThr
NM_001330615.4:c.729+10687_729+10692del NP_001317544.2:n.729+10687_729+10692del
NM_001354666.3:c.794_799del NP_001341595.2:p.Ile265_Pro267delinsThr
NM_001354667.3:c.794_799del NP_001341596.2:p.Ile265_Pro267delinsThr
NM_001374261.3:c.729+10687_729+10692del NP_001361190.2:n.729+10687_729+10692del
NM_001374262.3:c.729+10687_729+10692del NP_001361191.2:n.729+10687_729+10692del
NM_001374263.2:c.794_799del NP_001361192.2:p.Ile265_Pro267delinsThr
NM_001374264.2:c.794_799del NP_001361193.2:p.Ile265_Pro267delinsThr
NM_005037.7:c.794_799del NP_005028.5:p.Ile265_Pro267delinsThr
NM_138711.6:c.794_799del MANE Select NP_619725.3:p.Ile265_Pro267delinsThr
NM_138712.5:c.794_799del NP_619726.3:p.Ile265_Pro267delinsThr