Canonical Allele Identifier: CA11494136
Gene: PPARG HGNC NCBI

Linked Data

dbSNP Id: rs1175543
gnomAD v2: 3-12466433-A-G
gnomAD v3: 3-12424934-A-G
gnomAD v4: 3-12424934-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12424934A>G , CM000665.2:g.12424934A>G GRCh38
NC_000003.11:g.12466433A>G , CM000665.1:g.12466433A>G GRCh37
NC_000003.10:g.12441433A>G NCBI36
NG_011749.1:g.142085A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000681966.1:c.*434+7780A>G ENSP00000507572.1:n.*434+7780A>G
ENST00000681982.1:c.1180+7780A>G ENSP00000508065.1:n.1180+7780A>G
ENST00000682125.1:n.1225+7780A>G
ENST00000682446.1:c.1180+7780A>G ENSP00000506813.1:n.1180+7780A>G
ENST00000682494.1:n.4080+7780A>G
ENST00000682604.1:n.1423+7780A>G
ENST00000683586.1:c.1180+7780A>G ENSP00000507893.1:n.1180+7780A>G
ENST00000683599.1:n.229+7780A>G
ENST00000683699.1:c.820-8964A>G ENSP00000507823.1:n.820-8964A>G
ENST00000683700.1:c.1070+7436A>G ENSP00000508248.1:n.1070+7436A>G
ENST00000684065.1:c.*467-8964A>G ENSP00000508347.1:n.*467-8964A>G
ENST00000684094.1:n.1822+7780A>G
ENST00000684277.1:n.148+213A>G
ENST00000309576.11:c.1180+7780A>G ENSP00000312472.7:n.1180+7780A>G
ENST00000396999.3:c.*768+7780A>G ENSP00000380195.3:n.*768+7780A>G
ENST00000397000.6:c.730-8964A>G ENSP00000380196.2:n.730-8964A>G
ENST00000397010.7:c.1180+7780A>G ENSP00000380205.3:n.1180+7780A>G
ENST00000397015.7:c.1180+7780A>G ENSP00000380210.3:n.1180+7780A>G
ENST00000397026.7:c.1180+7780A>G ENSP00000380221.3:n.1180+7780A>G
ENST00000643197.2:c.1180+7780A>G ENSP00000495840.2:n.1180+7780A>G
ENST00000643888.2:c.1180+7780A>G ENSP00000494934.2:n.1180+7780A>G
ENST00000644622.2:c.1180+7780A>G ENSP00000494873.2:n.1180+7780A>G
ENST00000651735.1:c.1180+7780A>G MANE Select ENSP00000498313.1:n.1180+7780A>G
ENST00000652098.1:c.634+7780A>G ENSP00000498300.1:n.634+7780A>G
ENST00000652431.1:c.868+7780A>G ENSP00000498717.1:n.868+7780A>G
ENST00000287820.10:c.1270+7780A>G ENSP00000287820.6:n.1270+7780A>G
ENST00000309576.10:c.1186+7780A>G ENSP00000312472.6:n.1186+7780A>G
ENST00000397000.5:c.736-8964A>G ENSP00000380196.1:n.736-8964A>G
ENST00000397010.6:c.1186+7780A>G ENSP00000380205.2:n.1186+7780A>G
ENST00000397012.6:c.1186+7780A>G ENSP00000380207.2:n.1186+7780A>G
ENST00000397015.6:c.1186+7780A>G ENSP00000380210.2:n.1186+7780A>G
ENST00000397023.5:c.*1408+7780A>G ENSP00000380218.1:n.*1408+7780A>G
ENST00000397026.6:c.1204+7780A>G ENSP00000380221.2:n.1204+7780A>G
NM_005037.5:c.1186+7780A>G NP_005028.4:n.1186+7780A>G
NM_015869.4:c.1270+7780A>G NP_056953.2:n.1270+7780A>G
NM_138711.3:c.1186+7780A>G NP_619725.2:n.1186+7780A>G
NM_138712.3:c.1186+7780A>G NP_619726.2:n.1186+7780A>G
XM_011533840.1:c.1186+7780A>G XP_011532142.1:n.1186+7780A>G
XM_011533841.1:c.1186+7780A>G XP_011532143.1:n.1186+7780A>G
XM_011533842.1:c.1270+7780A>G XP_011532144.1:n.1270+7780A>G
XM_011533843.1:c.820-8964A>G XP_011532145.1:n.820-8964A>G
XM_011533844.1:c.736-8964A>G XP_011532146.1:n.736-8964A>G
NM_001330615.1:c.736-8964A>G NP_001317544.1:n.736-8964A>G
NM_001354666.1:c.1186+7780A>G NP_001341595.1:n.1186+7780A>G
NM_001354667.1:c.1186+7780A>G NP_001341596.1:n.1186+7780A>G
NM_001354669.1:c.553+7780A>G NP_001341598.1:n.553+7780A>G
XM_011533842.2:c.1270+7780A>G XP_011532144.1:n.1270+7780A>G
XM_011533843.2:c.820-8964A>G XP_011532145.1:n.820-8964A>G
XM_024453604.1:c.1186+7780A>G XP_024309372.1:n.1186+7780A>G
XM_024453605.1:c.1186+7780A>G XP_024309373.1:n.1186+7780A>G
XM_024453606.1:c.1186+7780A>G XP_024309374.1:n.1186+7780A>G
NM_001330615.2:c.736-8964A>G NP_001317544.1:n.736-8964A>G
NM_001354666.2:c.1186+7780A>G NP_001341595.1:n.1186+7780A>G
NM_001354667.2:c.1186+7780A>G NP_001341596.1:n.1186+7780A>G
NM_001354669.2:c.553+7780A>G NP_001341598.1:n.553+7780A>G
NM_001374261.1:c.736-8964A>G NP_001361190.1:n.736-8964A>G
NM_001374262.1:c.736-8964A>G NP_001361191.1:n.736-8964A>G
NM_001374263.1:c.1186+7780A>G NP_001361192.1:n.1186+7780A>G
NM_001374264.1:c.1186+7780A>G NP_001361193.1:n.1186+7780A>G
NM_001374265.1:c.820-8964A>G NP_001361194.1:n.820-8964A>G
NM_001374266.1:c.654-8964A>G NP_001361195.1:n.654-8964A>G
NM_005037.6:c.1186+7780A>G NP_005028.4:n.1186+7780A>G
NM_015869.5:c.1270+7780A>G NP_056953.2:n.1270+7780A>G
NM_138711.4:c.1186+7780A>G NP_619725.2:n.1186+7780A>G
NM_138712.4:c.1186+7780A>G NP_619726.2:n.1186+7780A>G
NM_001330615.4:c.730-8964A>G NP_001317544.2:n.730-8964A>G
NM_001354666.3:c.1180+7780A>G NP_001341595.2:n.1180+7780A>G
NM_001354667.3:c.1180+7780A>G NP_001341596.2:n.1180+7780A>G
NM_001374261.3:c.730-8964A>G NP_001361190.2:n.730-8964A>G
NM_001374262.3:c.730-8964A>G NP_001361191.2:n.730-8964A>G
NM_001374263.2:c.1180+7780A>G NP_001361192.2:n.1180+7780A>G
NM_001374264.2:c.1180+7780A>G NP_001361193.2:n.1180+7780A>G
NM_005037.7:c.1180+7780A>G NP_005028.5:n.1180+7780A>G
NM_138711.6:c.1180+7780A>G MANE Select NP_619725.3:n.1180+7780A>G
NM_138712.5:c.1180+7780A>G NP_619726.3:n.1180+7780A>G