Canonical Allele Identifier: CA1346087935
Gene: PPARG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12297259_12297262delinsAAGT , CM000665.2:g.12297259_12297262delinsAAGT GRCh38
NC_000003.11:g.12338758_12338761delinsAAGT , CM000665.1:g.12338758_12338761delinsAAGT GRCh37
NC_000003.10:g.12313758_12313761delinsAAGT NCBI36
NG_011749.1:g.14410_14413delinsAAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000681966.1:c.-83+9239_-83+9242delinsAAGT ENSP00000507572.1:n.-83+9239_-83+9242delinsAAGT
ENST00000681982.1:c.-171+8125_-171+8128delinsAAGT ENSP00000508065.1:n.-171+8125_-171+8128delinsAAGT
ENST00000309576.11:c.-83+9239_-83+9242delinsAAGT ENSP00000312472.7:n.-83+9239_-83+9242delinsAAGT
ENST00000397010.7:c.-83+9584_-83+9587delinsAAGT ENSP00000380205.3:n.-83+9584_-83+9587delinsAAGT
ENST00000397015.7:c.-9+9239_-9+9242delinsAAGT ENSP00000380210.3:n.-9+9239_-9+9242delinsAAGT
ENST00000397026.7:c.-344+8125_-344+8128delinsAAGT ENSP00000380221.3:n.-344+8125_-344+8128delinsAAGT
ENST00000397029.8:c.-9+9584_-9+9587delinsAAGT ENSP00000380224.4:n.-9+9584_-9+9587delinsAAGT
ENST00000455517.6:c.-9+8125_-9+8128delinsAAGT ENSP00000411931.2:n.-9+8125_-9+8128delinsAAGT
ENST00000643197.2:c.-411-4262_-411-4259delinsAAGT ENSP00000495840.2:n.-411-4262_-411-4259delinsAAGT
ENST00000643888.2:c.-171+9239_-171+9242delinsAAGT ENSP00000494934.2:n.-171+9239_-171+9242delinsAAGT
ENST00000644622.2:c.-483-610_-483-607delinsAAGT ENSP00000494873.2:n.-483-610_-483-607delinsAAGT
ENST00000651735.1:c.-83+8125_-83+8128delinsAAGT MANE Select ENSP00000498313.1:n.-83+8125_-83+8128delinsAAGT
ENST00000652098.1:c.-92+8125_-92+8128delinsAAGT ENSP00000498300.1:n.-92+8125_-92+8128delinsAAGT
ENST00000652431.1:c.-167+8125_-167+8128delinsAAGT ENSP00000498717.1:n.-167+8125_-167+8128delinsAAGT
ENST00000652522.1:c.-154-610_-154-607delinsAAGT ENSP00000498500.1:n.-154-610_-154-607delinsAAGT
ENST00000309576.10:c.-77+9239_-77+9242delinsAAGT ENSP00000312472.6:n.-77+9239_-77+9242delinsAAGT
ENST00000397010.6:c.-77+9584_-77+9587delinsAAGT ENSP00000380205.2:n.-77+9584_-77+9587delinsAAGT
ENST00000397012.6:c.-77+8125_-77+8128delinsAAGT ENSP00000380207.2:n.-77+8125_-77+8128delinsAAGT
ENST00000397015.6:c.-3+9239_-3+9242delinsAAGT ENSP00000380210.2:n.-3+9239_-3+9242delinsAAGT
ENST00000397026.6:c.-320+8125_-320+8128delinsAAGT ENSP00000380221.2:n.-320+8125_-320+8128delinsAAGT
ENST00000397029.7:c.-3+9584_-3+9587delinsAAGT ENSP00000380224.3:n.-3+9584_-3+9587delinsAAGT
ENST00000455517.5:c.-3+8125_-3+8128delinsAAGT ENSP00000411931.1:n.-3+8125_-3+8128delinsAAGT
ENST00000497594.5:n.24+8125_24+8128delinsAAGT
NM_005037.5:c.-3+9239_-3+9242delinsAAGT NP_005028.4:n.-3+9239_-3+9242delinsAAGT
NM_138711.3:c.-77+8125_-77+8128delinsAAGT NP_619725.2:n.-77+8125_-77+8128delinsAAGT
NM_138712.3:c.-77+9239_-77+9242delinsAAGT NP_619726.2:n.-77+9239_-77+9242delinsAAGT
XM_011533841.1:c.-3+8125_-3+8128delinsAAGT XP_011532143.1:n.-3+8125_-3+8128delinsAAGT
XM_011533844.1:c.-77+8125_-77+8128delinsAAGT XP_011532146.1:n.-77+8125_-77+8128delinsAAGT
NM_001354666.1:c.-77+9584_-77+9587delinsAAGT NP_001341595.1:n.-77+9584_-77+9587delinsAAGT
NM_001354667.1:c.-3+8125_-3+8128delinsAAGT NP_001341596.1:n.-3+8125_-3+8128delinsAAGT
NM_001354669.1:c.-510+9239_-510+9242delinsAAGT NP_001341598.1:n.-510+9239_-510+9242delinsAAGT
NM_001354670.1:c.-77+8125_-77+8128delinsAAGT NP_001341599.1:n.-77+8125_-77+8128delinsAAGT
NM_001330615.2:c.-77+8125_-77+8128delinsAAGT NP_001317544.1:n.-77+8125_-77+8128delinsAAGT
NM_001354666.2:c.-77+9584_-77+9587delinsAAGT NP_001341595.1:n.-77+9584_-77+9587delinsAAGT
NM_001354667.2:c.-3+8125_-3+8128delinsAAGT NP_001341596.1:n.-3+8125_-3+8128delinsAAGT
NM_001354669.2:c.-510+9239_-510+9242delinsAAGT NP_001341598.1:n.-510+9239_-510+9242delinsAAGT
NM_001354670.2:c.-77+8125_-77+8128delinsAAGT NP_001341599.1:n.-77+8125_-77+8128delinsAAGT
NM_001374261.1:c.-77+9239_-77+9242delinsAAGT NP_001361190.1:n.-77+9239_-77+9242delinsAAGT
NM_001374262.1:c.-165+8125_-165+8128delinsAAGT NP_001361191.1:n.-165+8125_-165+8128delinsAAGT
NM_001374266.1:c.-77+8125_-77+8128delinsAAGT NP_001361195.1:n.-77+8125_-77+8128delinsAAGT
NM_005037.6:c.-3+9239_-3+9242delinsAAGT NP_005028.4:n.-3+9239_-3+9242delinsAAGT
NM_138711.4:c.-77+8125_-77+8128delinsAAGT NP_619725.2:n.-77+8125_-77+8128delinsAAGT
NM_138712.4:c.-77+9239_-77+9242delinsAAGT NP_619726.2:n.-77+9239_-77+9242delinsAAGT
NM_001330615.4:c.-83+8125_-83+8128delinsAAGT NP_001317544.2:n.-83+8125_-83+8128delinsAAGT
NM_001354666.3:c.-83+9584_-83+9587delinsAAGT NP_001341595.2:n.-83+9584_-83+9587delinsAAGT
NM_001354667.3:c.-9+8125_-9+8128delinsAAGT NP_001341596.2:n.-9+8125_-9+8128delinsAAGT
NM_001374261.3:c.-83+9239_-83+9242delinsAAGT NP_001361190.2:n.-83+9239_-83+9242delinsAAGT
NM_001374262.3:c.-171+8125_-171+8128delinsAAGT NP_001361191.2:n.-171+8125_-171+8128delinsAAGT
NM_005037.7:c.-9+9239_-9+9242delinsAAGT NP_005028.5:n.-9+9239_-9+9242delinsAAGT
NM_138711.6:c.-83+8125_-83+8128delinsAAGT MANE Select NP_619725.3:n.-83+8125_-83+8128delinsAAGT
NM_138712.5:c.-83+9239_-83+9242delinsAAGT NP_619726.3:n.-83+9239_-83+9242delinsAAGT