Canonical Allele Identifier: CA1346089895
Gene: PPARG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12299510_12299516delinsATATATT , CM000665.2:g.12299510_12299516delinsATATATT GRCh38
NC_000003.11:g.12341009_12341015delinsATATATT , CM000665.1:g.12341009_12341015delinsATATATT GRCh37
NC_000003.10:g.12316009_12316015delinsATATATT NCBI36
NG_011749.1:g.16661_16667delinsATATATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000681966.1:c.-83+11490_-83+11496delinsATATATT ENSP00000507572.1:n.-83+11490_-83+11496delinsATATATT
ENST00000681982.1:c.-171+10376_-171+10382delinsATATATT ENSP00000508065.1:n.-171+10376_-171+10382delinsATATATT
ENST00000309576.11:c.-83+11490_-83+11496delinsATATATT ENSP00000312472.7:n.-83+11490_-83+11496delinsATATATT
ENST00000397010.7:c.-83+11835_-83+11841delinsATATATT ENSP00000380205.3:n.-83+11835_-83+11841delinsATATATT
ENST00000397015.7:c.-9+11490_-9+11496delinsATATATT ENSP00000380210.3:n.-9+11490_-9+11496delinsATATATT
ENST00000397026.7:c.-344+10376_-344+10382delinsATATATT ENSP00000380221.3:n.-344+10376_-344+10382delinsATATATT
ENST00000397029.8:c.-9+11835_-9+11841delinsATATATT ENSP00000380224.4:n.-9+11835_-9+11841delinsATATATT
ENST00000455517.6:c.-9+10376_-9+10382delinsATATATT ENSP00000411931.2:n.-9+10376_-9+10382delinsATATATT
ENST00000643197.2:c.-411-2011_-411-2005delinsATATATT ENSP00000495840.2:n.-411-2011_-411-2005delinsATATATT
ENST00000643888.2:c.-171+11490_-171+11496delinsATATATT ENSP00000494934.2:n.-171+11490_-171+11496delinsATATATT
ENST00000644622.2:c.-412+1570_-412+1576delinsATATATT ENSP00000494873.2:n.-412+1570_-412+1576delinsATATATT
ENST00000651735.1:c.-83+10376_-83+10382delinsATATATT MANE Select ENSP00000498313.1:n.-83+10376_-83+10382delinsATATATT
ENST00000652098.1:c.-92+10376_-92+10382delinsATATATT ENSP00000498300.1:n.-92+10376_-92+10382delinsATATATT
ENST00000652431.1:c.-167+10376_-167+10382delinsATATATT ENSP00000498717.1:n.-167+10376_-167+10382delinsATATATT
ENST00000652522.1:c.-83+1570_-83+1576delinsATATATT ENSP00000498500.1:n.-83+1570_-83+1576delinsATATATT
ENST00000309576.10:c.-77+11490_-77+11496delinsATATATT ENSP00000312472.6:n.-77+11490_-77+11496delinsATATATT
ENST00000397010.6:c.-77+11835_-77+11841delinsATATATT ENSP00000380205.2:n.-77+11835_-77+11841delinsATATATT
ENST00000397012.6:c.-77+10376_-77+10382delinsATATATT ENSP00000380207.2:n.-77+10376_-77+10382delinsATATATT
ENST00000397015.6:c.-3+11490_-3+11496delinsATATATT ENSP00000380210.2:n.-3+11490_-3+11496delinsATATATT
ENST00000397026.6:c.-320+10376_-320+10382delinsATATATT ENSP00000380221.2:n.-320+10376_-320+10382delinsATATATT
ENST00000397029.7:c.-3+11835_-3+11841delinsATATATT ENSP00000380224.3:n.-3+11835_-3+11841delinsATATATT
ENST00000455517.5:c.-3+10376_-3+10382delinsATATATT ENSP00000411931.1:n.-3+10376_-3+10382delinsATATATT
ENST00000497594.5:n.24+10376_24+10382delinsATATATT
NM_005037.5:c.-3+11490_-3+11496delinsATATATT NP_005028.4:n.-3+11490_-3+11496delinsATATATT
NM_138711.3:c.-77+10376_-77+10382delinsATATATT NP_619725.2:n.-77+10376_-77+10382delinsATATATT
NM_138712.3:c.-77+11490_-77+11496delinsATATATT NP_619726.2:n.-77+11490_-77+11496delinsATATATT
XM_011533841.1:c.-3+10376_-3+10382delinsATATATT XP_011532143.1:n.-3+10376_-3+10382delinsATATATT
XM_011533844.1:c.-77+10376_-77+10382delinsATATATT XP_011532146.1:n.-77+10376_-77+10382delinsATATATT
NM_001354666.1:c.-77+11835_-77+11841delinsATATATT NP_001341595.1:n.-77+11835_-77+11841delinsATATATT
NM_001354667.1:c.-3+10376_-3+10382delinsATATATT NP_001341596.1:n.-3+10376_-3+10382delinsATATATT
NM_001354669.1:c.-510+11490_-510+11496delinsATATATT NP_001341598.1:n.-510+11490_-510+11496delinsATATATT
NM_001354670.1:c.-77+10376_-77+10382delinsATATATT NP_001341599.1:n.-77+10376_-77+10382delinsATATATT
NM_001330615.2:c.-77+10376_-77+10382delinsATATATT NP_001317544.1:n.-77+10376_-77+10382delinsATATATT
NM_001354666.2:c.-77+11835_-77+11841delinsATATATT NP_001341595.1:n.-77+11835_-77+11841delinsATATATT
NM_001354667.2:c.-3+10376_-3+10382delinsATATATT NP_001341596.1:n.-3+10376_-3+10382delinsATATATT
NM_001354669.2:c.-510+11490_-510+11496delinsATATATT NP_001341598.1:n.-510+11490_-510+11496delinsATATATT
NM_001354670.2:c.-77+10376_-77+10382delinsATATATT NP_001341599.1:n.-77+10376_-77+10382delinsATATATT
NM_001374261.1:c.-77+11490_-77+11496delinsATATATT NP_001361190.1:n.-77+11490_-77+11496delinsATATATT
NM_001374262.1:c.-165+10376_-165+10382delinsATATATT NP_001361191.1:n.-165+10376_-165+10382delinsATATATT
NM_001374266.1:c.-77+10376_-77+10382delinsATATATT NP_001361195.1:n.-77+10376_-77+10382delinsATATATT
NM_005037.6:c.-3+11490_-3+11496delinsATATATT NP_005028.4:n.-3+11490_-3+11496delinsATATATT
NM_138711.4:c.-77+10376_-77+10382delinsATATATT NP_619725.2:n.-77+10376_-77+10382delinsATATATT
NM_138712.4:c.-77+11490_-77+11496delinsATATATT NP_619726.2:n.-77+11490_-77+11496delinsATATATT
NM_001330615.4:c.-83+10376_-83+10382delinsATATATT NP_001317544.2:n.-83+10376_-83+10382delinsATATATT
NM_001354666.3:c.-83+11835_-83+11841delinsATATATT NP_001341595.2:n.-83+11835_-83+11841delinsATATATT
NM_001354667.3:c.-9+10376_-9+10382delinsATATATT NP_001341596.2:n.-9+10376_-9+10382delinsATATATT
NM_001374261.3:c.-83+11490_-83+11496delinsATATATT NP_001361190.2:n.-83+11490_-83+11496delinsATATATT
NM_001374262.3:c.-171+10376_-171+10382delinsATATATT NP_001361191.2:n.-171+10376_-171+10382delinsATATATT
NM_005037.7:c.-9+11490_-9+11496delinsATATATT NP_005028.5:n.-9+11490_-9+11496delinsATATATT
NM_138711.6:c.-83+10376_-83+10382delinsATATATT MANE Select NP_619725.3:n.-83+10376_-83+10382delinsATATATT
NM_138712.5:c.-83+11490_-83+11496delinsATATATT NP_619726.3:n.-83+11490_-83+11496delinsATATATT
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