Canonical Allele Identifier: CA1346088142
Gene: PPARG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12297482_12297484delinsTTC , CM000665.2:g.12297482_12297484delinsTTC GRCh38
NC_000003.11:g.12338981_12338983delinsTTC , CM000665.1:g.12338981_12338983delinsTTC GRCh37
NC_000003.10:g.12313981_12313983delinsTTC NCBI36
NG_011749.1:g.14633_14635delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000681966.1:c.-83+9462_-83+9464delinsTTC ENSP00000507572.1:n.-83+9462_-83+9464delinsTTC
ENST00000681982.1:c.-171+8348_-171+8350delinsTTC ENSP00000508065.1:n.-171+8348_-171+8350delinsTTC
ENST00000309576.11:c.-83+9462_-83+9464delinsTTC ENSP00000312472.7:n.-83+9462_-83+9464delinsTTC
ENST00000397010.7:c.-83+9807_-83+9809delinsTTC ENSP00000380205.3:n.-83+9807_-83+9809delinsTTC
ENST00000397015.7:c.-9+9462_-9+9464delinsTTC ENSP00000380210.3:n.-9+9462_-9+9464delinsTTC
ENST00000397026.7:c.-344+8348_-344+8350delinsTTC ENSP00000380221.3:n.-344+8348_-344+8350delinsTTC
ENST00000397029.8:c.-9+9807_-9+9809delinsTTC ENSP00000380224.4:n.-9+9807_-9+9809delinsTTC
ENST00000455517.6:c.-9+8348_-9+8350delinsTTC ENSP00000411931.2:n.-9+8348_-9+8350delinsTTC
ENST00000643197.2:c.-411-4039_-411-4037delinsTTC ENSP00000495840.2:n.-411-4039_-411-4037delinsTTC
ENST00000643888.2:c.-171+9462_-171+9464delinsTTC ENSP00000494934.2:n.-171+9462_-171+9464delinsTTC
ENST00000644622.2:c.-483-387_-483-385delinsTTC ENSP00000494873.2:n.-483-387_-483-385delinsTTC
ENST00000651735.1:c.-83+8348_-83+8350delinsTTC MANE Select ENSP00000498313.1:n.-83+8348_-83+8350delinsTTC
ENST00000652098.1:c.-92+8348_-92+8350delinsTTC ENSP00000498300.1:n.-92+8348_-92+8350delinsTTC
ENST00000652431.1:c.-167+8348_-167+8350delinsTTC ENSP00000498717.1:n.-167+8348_-167+8350delinsTTC
ENST00000652522.1:c.-154-387_-154-385delinsTTC ENSP00000498500.1:n.-154-387_-154-385delinsTTC
ENST00000309576.10:c.-77+9462_-77+9464delinsTTC ENSP00000312472.6:n.-77+9462_-77+9464delinsTTC
ENST00000397010.6:c.-77+9807_-77+9809delinsTTC ENSP00000380205.2:n.-77+9807_-77+9809delinsTTC
ENST00000397012.6:c.-77+8348_-77+8350delinsTTC ENSP00000380207.2:n.-77+8348_-77+8350delinsTTC
ENST00000397015.6:c.-3+9462_-3+9464delinsTTC ENSP00000380210.2:n.-3+9462_-3+9464delinsTTC
ENST00000397026.6:c.-320+8348_-320+8350delinsTTC ENSP00000380221.2:n.-320+8348_-320+8350delinsTTC
ENST00000397029.7:c.-3+9807_-3+9809delinsTTC ENSP00000380224.3:n.-3+9807_-3+9809delinsTTC
ENST00000455517.5:c.-3+8348_-3+8350delinsTTC ENSP00000411931.1:n.-3+8348_-3+8350delinsTTC
ENST00000497594.5:n.24+8348_24+8350delinsTTC
NM_005037.5:c.-3+9462_-3+9464delinsTTC NP_005028.4:n.-3+9462_-3+9464delinsTTC
NM_138711.3:c.-77+8348_-77+8350delinsTTC NP_619725.2:n.-77+8348_-77+8350delinsTTC
NM_138712.3:c.-77+9462_-77+9464delinsTTC NP_619726.2:n.-77+9462_-77+9464delinsTTC
XM_011533841.1:c.-3+8348_-3+8350delinsTTC XP_011532143.1:n.-3+8348_-3+8350delinsTTC
XM_011533844.1:c.-77+8348_-77+8350delinsTTC XP_011532146.1:n.-77+8348_-77+8350delinsTTC
NM_001354666.1:c.-77+9807_-77+9809delinsTTC NP_001341595.1:n.-77+9807_-77+9809delinsTTC
NM_001354667.1:c.-3+8348_-3+8350delinsTTC NP_001341596.1:n.-3+8348_-3+8350delinsTTC
NM_001354669.1:c.-510+9462_-510+9464delinsTTC NP_001341598.1:n.-510+9462_-510+9464delinsTTC
NM_001354670.1:c.-77+8348_-77+8350delinsTTC NP_001341599.1:n.-77+8348_-77+8350delinsTTC
NM_001330615.2:c.-77+8348_-77+8350delinsTTC NP_001317544.1:n.-77+8348_-77+8350delinsTTC
NM_001354666.2:c.-77+9807_-77+9809delinsTTC NP_001341595.1:n.-77+9807_-77+9809delinsTTC
NM_001354667.2:c.-3+8348_-3+8350delinsTTC NP_001341596.1:n.-3+8348_-3+8350delinsTTC
NM_001354669.2:c.-510+9462_-510+9464delinsTTC NP_001341598.1:n.-510+9462_-510+9464delinsTTC
NM_001354670.2:c.-77+8348_-77+8350delinsTTC NP_001341599.1:n.-77+8348_-77+8350delinsTTC
NM_001374261.1:c.-77+9462_-77+9464delinsTTC NP_001361190.1:n.-77+9462_-77+9464delinsTTC
NM_001374262.1:c.-165+8348_-165+8350delinsTTC NP_001361191.1:n.-165+8348_-165+8350delinsTTC
NM_001374266.1:c.-77+8348_-77+8350delinsTTC NP_001361195.1:n.-77+8348_-77+8350delinsTTC
NM_005037.6:c.-3+9462_-3+9464delinsTTC NP_005028.4:n.-3+9462_-3+9464delinsTTC
NM_138711.4:c.-77+8348_-77+8350delinsTTC NP_619725.2:n.-77+8348_-77+8350delinsTTC
NM_138712.4:c.-77+9462_-77+9464delinsTTC NP_619726.2:n.-77+9462_-77+9464delinsTTC
NM_001330615.4:c.-83+8348_-83+8350delinsTTC NP_001317544.2:n.-83+8348_-83+8350delinsTTC
NM_001354666.3:c.-83+9807_-83+9809delinsTTC NP_001341595.2:n.-83+9807_-83+9809delinsTTC
NM_001354667.3:c.-9+8348_-9+8350delinsTTC NP_001341596.2:n.-9+8348_-9+8350delinsTTC
NM_001374261.3:c.-83+9462_-83+9464delinsTTC NP_001361190.2:n.-83+9462_-83+9464delinsTTC
NM_001374262.3:c.-171+8348_-171+8350delinsTTC NP_001361191.2:n.-171+8348_-171+8350delinsTTC
NM_005037.7:c.-9+9462_-9+9464delinsTTC NP_005028.5:n.-9+9462_-9+9464delinsTTC
NM_138711.6:c.-83+8348_-83+8350delinsTTC MANE Select NP_619725.3:n.-83+8348_-83+8350delinsTTC
NM_138712.5:c.-83+9462_-83+9464delinsTTC NP_619726.3:n.-83+9462_-83+9464delinsTTC