Canonical Allele Identifier: CA2755251141

Gene: PPARG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12297302del , CM000665.2:g.12297302del	GRCh38
NC_000003.11:g.12338801del , CM000665.1:g.12338801del	GRCh37
NC_000003.10:g.12313801del	NCBI36
NG_011749.1:g.14453del

Transcript Alleles

HGVS	Amino-acid change
ENST00000681966.1:c.-83+9282del	ENSP00000507572.1:n.-83+9282del
ENST00000681982.1:c.-171+8168del	ENSP00000508065.1:n.-171+8168del
ENST00000309576.11:c.-83+9282del	ENSP00000312472.7:n.-83+9282del
ENST00000397010.7:c.-83+9627del	ENSP00000380205.3:n.-83+9627del
ENST00000397015.7:c.-9+9282del	ENSP00000380210.3:n.-9+9282del
ENST00000397026.7:c.-344+8168del	ENSP00000380221.3:n.-344+8168del
ENST00000397029.8:c.-9+9627del	ENSP00000380224.4:n.-9+9627del
ENST00000455517.6:c.-9+8168del	ENSP00000411931.2:n.-9+8168del
ENST00000643197.2:c.-411-4219del	ENSP00000495840.2:n.-411-4219del
ENST00000643888.2:c.-171+9282del	ENSP00000494934.2:n.-171+9282del
ENST00000644622.2:c.-483-567del	ENSP00000494873.2:n.-483-567del
ENST00000651735.1:c.-83+8168del MANE Select	ENSP00000498313.1:n.-83+8168del
ENST00000652098.1:c.-92+8168del	ENSP00000498300.1:n.-92+8168del
ENST00000652431.1:c.-167+8168del	ENSP00000498717.1:n.-167+8168del
ENST00000652522.1:c.-154-567del	ENSP00000498500.1:n.-154-567del
ENST00000309576.10:c.-77+9282del	ENSP00000312472.6:n.-77+9282del
ENST00000397010.6:c.-77+9627del	ENSP00000380205.2:n.-77+9627del
ENST00000397012.6:c.-77+8168del	ENSP00000380207.2:n.-77+8168del
ENST00000397015.6:c.-3+9282del	ENSP00000380210.2:n.-3+9282del
ENST00000397026.6:c.-320+8168del	ENSP00000380221.2:n.-320+8168del
ENST00000397029.7:c.-3+9627del	ENSP00000380224.3:n.-3+9627del
ENST00000455517.5:c.-3+8168del	ENSP00000411931.1:n.-3+8168del
ENST00000497594.5:n.24+8168del
NM_005037.5:c.-3+9282del	NP_005028.4:n.-3+9282del
NM_138711.3:c.-77+8168del	NP_619725.2:n.-77+8168del
NM_138712.3:c.-77+9282del	NP_619726.2:n.-77+9282del
XM_011533841.1:c.-3+8168del	XP_011532143.1:n.-3+8168del
XM_011533844.1:c.-77+8168del	XP_011532146.1:n.-77+8168del
NM_001354666.1:c.-77+9627del	NP_001341595.1:n.-77+9627del
NM_001354667.1:c.-3+8168del	NP_001341596.1:n.-3+8168del
NM_001354669.1:c.-510+9282del	NP_001341598.1:n.-510+9282del
NM_001354670.1:c.-77+8168del	NP_001341599.1:n.-77+8168del
NM_001330615.2:c.-77+8168del	NP_001317544.1:n.-77+8168del
NM_001354666.2:c.-77+9627del	NP_001341595.1:n.-77+9627del
NM_001354667.2:c.-3+8168del	NP_001341596.1:n.-3+8168del
NM_001354669.2:c.-510+9282del	NP_001341598.1:n.-510+9282del
NM_001354670.2:c.-77+8168del	NP_001341599.1:n.-77+8168del
NM_001374261.1:c.-77+9282del	NP_001361190.1:n.-77+9282del
NM_001374262.1:c.-165+8168del	NP_001361191.1:n.-165+8168del
NM_001374266.1:c.-77+8168del	NP_001361195.1:n.-77+8168del
NM_005037.6:c.-3+9282del	NP_005028.4:n.-3+9282del
NM_138711.4:c.-77+8168del	NP_619725.2:n.-77+8168del
NM_138712.4:c.-77+9282del	NP_619726.2:n.-77+9282del
NM_001330615.4:c.-83+8168del	NP_001317544.2:n.-83+8168del
NM_001354666.3:c.-83+9627del	NP_001341595.2:n.-83+9627del
NM_001354667.3:c.-9+8168del	NP_001341596.2:n.-9+8168del
NM_001374261.3:c.-83+9282del	NP_001361190.2:n.-83+9282del
NM_001374262.3:c.-171+8168del	NP_001361191.2:n.-171+8168del
NM_005037.7:c.-9+9282del	NP_005028.5:n.-9+9282del
NM_138711.6:c.-83+8168del MANE Select	NP_619725.3:n.-83+8168del
NM_138712.5:c.-83+9282del	NP_619726.3:n.-83+9282del