Canonical Allele Identifier: CA70171073

Gene: PPARG

Linked Data

• dbSNP Id: rs1053391068
• MyVariant Identifiers: chr3:g.12340138G>T (hg19) ; chr3:g.12298639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12298639G>T , CM000665.2:g.12298639G>T	GRCh38
NC_000003.11:g.12340138G>T , CM000665.1:g.12340138G>T	GRCh37
NC_000003.10:g.12315138G>T	NCBI36
NG_011749.1:g.15790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681966.1:c.-83+10619G>T	ENSP00000507572.1:n.-83+10619G>T
ENST00000681982.1:c.-171+9505G>T	ENSP00000508065.1:n.-171+9505G>T
ENST00000309576.11:c.-83+10619G>T	ENSP00000312472.7:n.-83+10619G>T
ENST00000397010.7:c.-83+10964G>T	ENSP00000380205.3:n.-83+10964G>T
ENST00000397015.7:c.-9+10619G>T	ENSP00000380210.3:n.-9+10619G>T
ENST00000397026.7:c.-344+9505G>T	ENSP00000380221.3:n.-344+9505G>T
ENST00000397029.8:c.-9+10964G>T	ENSP00000380224.4:n.-9+10964G>T
ENST00000455517.6:c.-9+9505G>T	ENSP00000411931.2:n.-9+9505G>T
ENST00000643197.2:c.-411-2882G>T	ENSP00000495840.2:n.-411-2882G>T
ENST00000643888.2:c.-171+10619G>T	ENSP00000494934.2:n.-171+10619G>T
ENST00000644622.2:c.-412+699G>T	ENSP00000494873.2:n.-412+699G>T
ENST00000651735.1:c.-83+9505G>T MANE Select	ENSP00000498313.1:n.-83+9505G>T
ENST00000652098.1:c.-92+9505G>T	ENSP00000498300.1:n.-92+9505G>T
ENST00000652431.1:c.-167+9505G>T	ENSP00000498717.1:n.-167+9505G>T
ENST00000652522.1:c.-83+699G>T	ENSP00000498500.1:n.-83+699G>T
ENST00000309576.10:c.-77+10619G>T	ENSP00000312472.6:n.-77+10619G>T
ENST00000397010.6:c.-77+10964G>T	ENSP00000380205.2:n.-77+10964G>T
ENST00000397012.6:c.-77+9505G>T	ENSP00000380207.2:n.-77+9505G>T
ENST00000397015.6:c.-3+10619G>T	ENSP00000380210.2:n.-3+10619G>T
ENST00000397026.6:c.-320+9505G>T	ENSP00000380221.2:n.-320+9505G>T
ENST00000397029.7:c.-3+10964G>T	ENSP00000380224.3:n.-3+10964G>T
ENST00000455517.5:c.-3+9505G>T	ENSP00000411931.1:n.-3+9505G>T
ENST00000497594.5:n.24+9505G>T
NM_005037.5:c.-3+10619G>T	NP_005028.4:n.-3+10619G>T
NM_138711.3:c.-77+9505G>T	NP_619725.2:n.-77+9505G>T
NM_138712.3:c.-77+10619G>T	NP_619726.2:n.-77+10619G>T
XM_011533841.1:c.-3+9505G>T	XP_011532143.1:n.-3+9505G>T
XM_011533844.1:c.-77+9505G>T	XP_011532146.1:n.-77+9505G>T
NM_001354666.1:c.-77+10964G>T	NP_001341595.1:n.-77+10964G>T
NM_001354667.1:c.-3+9505G>T	NP_001341596.1:n.-3+9505G>T
NM_001354669.1:c.-510+10619G>T	NP_001341598.1:n.-510+10619G>T
NM_001354670.1:c.-77+9505G>T	NP_001341599.1:n.-77+9505G>T
NM_001330615.2:c.-77+9505G>T	NP_001317544.1:n.-77+9505G>T
NM_001354666.2:c.-77+10964G>T	NP_001341595.1:n.-77+10964G>T
NM_001354667.2:c.-3+9505G>T	NP_001341596.1:n.-3+9505G>T
NM_001354669.2:c.-510+10619G>T	NP_001341598.1:n.-510+10619G>T
NM_001354670.2:c.-77+9505G>T	NP_001341599.1:n.-77+9505G>T
NM_001374261.1:c.-77+10619G>T	NP_001361190.1:n.-77+10619G>T
NM_001374262.1:c.-165+9505G>T	NP_001361191.1:n.-165+9505G>T
NM_001374266.1:c.-77+9505G>T	NP_001361195.1:n.-77+9505G>T
NM_005037.6:c.-3+10619G>T	NP_005028.4:n.-3+10619G>T
NM_138711.4:c.-77+9505G>T	NP_619725.2:n.-77+9505G>T
NM_138712.4:c.-77+10619G>T	NP_619726.2:n.-77+10619G>T
NM_001330615.4:c.-83+9505G>T	NP_001317544.2:n.-83+9505G>T
NM_001354666.3:c.-83+10964G>T	NP_001341595.2:n.-83+10964G>T
NM_001354667.3:c.-9+9505G>T	NP_001341596.2:n.-9+9505G>T
NM_001374261.3:c.-83+10619G>T	NP_001361190.2:n.-83+10619G>T
NM_001374262.3:c.-171+9505G>T	NP_001361191.2:n.-171+9505G>T
NM_005037.7:c.-9+10619G>T	NP_005028.5:n.-9+10619G>T
NM_138711.6:c.-83+9505G>T MANE Select	NP_619725.3:n.-83+9505G>T
NM_138712.5:c.-83+10619G>T	NP_619726.3:n.-83+10619G>T