Canonical Allele Identifier: CA351619328
Gene: PPARG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12416806C>G , CM000665.2:g.12416806C>G GRCh38
NC_000003.11:g.12458305C>G , CM000665.1:g.12458305C>G GRCh37
NC_000003.10:g.12433305C>G NCBI36
NG_011749.1:g.133957C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000681966.1:c.*86C>G ENSP00000507572.1:n.*86C>G
ENST00000681982.1:c.832C>G ENSP00000508065.1:p.Arg278Gly
ENST00000682125.1:n.877C>G
ENST00000682446.1:c.832C>G ENSP00000506813.1:p.Arg278Gly
ENST00000682494.1:n.3732C>G
ENST00000682604.1:n.1075C>G
ENST00000683586.1:c.832C>G ENSP00000507893.1:p.Arg278Gly
ENST00000683699.1:c.819+10725C>G ENSP00000507823.1:n.819+10725C>G
ENST00000683700.1:c.685C>G ENSP00000508248.1:p.Arg229Gly
ENST00000684065.1:c.*466+10725C>G ENSP00000508347.1:n.*466+10725C>G
ENST00000684094.1:n.1474C>G
ENST00000309576.11:c.832C>G ENSP00000312472.7:p.Arg278Gly
ENST00000396999.3:c.*420C>G ENSP00000380195.3:n.*420C>G
ENST00000397000.6:c.729+10725C>G ENSP00000380196.2:n.729+10725C>G
ENST00000397010.7:c.832C>G ENSP00000380205.3:p.Arg278Gly
ENST00000397015.7:c.832C>G ENSP00000380210.3:p.Arg278Gly
ENST00000397026.7:c.832C>G ENSP00000380221.3:p.Arg278Gly
ENST00000643197.2:c.832C>G ENSP00000495840.2:p.Arg278Gly
ENST00000643888.2:c.832C>G ENSP00000494934.2:p.Arg278Gly
ENST00000644622.2:c.832C>G ENSP00000494873.2:p.Arg278Gly
ENST00000651735.1:c.832C>G MANE Select ENSP00000498313.1:p.Arg278Gly
ENST00000652098.1:c.286C>G ENSP00000498300.1:p.Arg96Gly
ENST00000652431.1:c.520C>G ENSP00000498717.1:p.Arg174Gly
ENST00000652522.1:c.832C>G ENSP00000498500.1:p.Arg278Gly
ENST00000287820.10:c.922C>G ENSP00000287820.6:p.Arg308Gly
ENST00000309576.10:c.838C>G ENSP00000312472.6:p.Arg280Gly
ENST00000396999.2:c.981C>G ENSP00000380195.2:n.981C>G
ENST00000397000.5:c.735+10725C>G ENSP00000380196.1:n.735+10725C>G
ENST00000397010.6:c.838C>G ENSP00000380205.2:p.Arg280Gly
ENST00000397012.6:c.838C>G ENSP00000380207.2:p.Arg280Gly
ENST00000397015.6:c.838C>G ENSP00000380210.2:p.Arg280Gly
ENST00000397023.5:c.*1060C>G ENSP00000380218.1:n.*1060C>G
ENST00000397026.6:c.856C>G ENSP00000380221.2:p.Arg286Gly
NM_005037.5:c.838C>G NP_005028.4:p.Arg280Gly
NM_015869.4:c.922C>G NP_056953.2:p.Arg308Gly
NM_138711.3:c.838C>G NP_619725.2:p.Arg280Gly
NM_138712.3:c.838C>G NP_619726.2:p.Arg280Gly
XM_011533840.1:c.838C>G XP_011532142.1:p.Arg280Gly
XM_011533841.1:c.838C>G XP_011532143.1:p.Arg280Gly
XM_011533842.1:c.922C>G XP_011532144.1:p.Arg308Gly
XM_011533843.1:c.819+10725C>G XP_011532145.1:n.819+10725C>G
XM_011533844.1:c.735+10725C>G XP_011532146.1:n.735+10725C>G
NM_001330615.1:c.735+10725C>G NP_001317544.1:n.735+10725C>G
NM_001354666.1:c.838C>G NP_001341595.1:p.Arg280Gly
NM_001354667.1:c.838C>G NP_001341596.1:p.Arg280Gly
NM_001354669.1:c.205C>G NP_001341598.1:p.Arg69Gly
XM_011533842.2:c.922C>G XP_011532144.1:p.Arg308Gly
XM_011533843.2:c.819+10725C>G XP_011532145.1:n.819+10725C>G
XM_024453604.1:c.838C>G XP_024309372.1:p.Arg280Gly
XM_024453605.1:c.838C>G XP_024309373.1:p.Arg280Gly
XM_024453606.1:c.838C>G XP_024309374.1:p.Arg280Gly
NM_001330615.2:c.735+10725C>G NP_001317544.1:n.735+10725C>G
NM_001354666.2:c.838C>G NP_001341595.1:p.Arg280Gly
NM_001354667.2:c.838C>G NP_001341596.1:p.Arg280Gly
NM_001354669.2:c.205C>G NP_001341598.1:p.Arg69Gly
NM_001374261.1:c.735+10725C>G NP_001361190.1:n.735+10725C>G
NM_001374262.1:c.735+10725C>G NP_001361191.1:n.735+10725C>G
NM_001374263.1:c.838C>G NP_001361192.1:p.Arg280Gly
NM_001374264.1:c.838C>G NP_001361193.1:p.Arg280Gly
NM_001374265.1:c.819+10725C>G NP_001361194.1:n.819+10725C>G
NM_001374266.1:c.653+10807C>G NP_001361195.1:n.653+10807C>G
NM_005037.6:c.838C>G NP_005028.4:p.Arg280Gly
NM_015869.5:c.922C>G NP_056953.2:p.Arg308Gly
NM_138711.4:c.838C>G NP_619725.2:p.Arg280Gly
NM_138712.4:c.838C>G NP_619726.2:p.Arg280Gly
NM_001330615.4:c.729+10725C>G NP_001317544.2:n.729+10725C>G
NM_001354666.3:c.832C>G NP_001341595.2:p.Arg278Gly
NM_001354667.3:c.832C>G NP_001341596.2:p.Arg278Gly
NM_001374261.3:c.729+10725C>G NP_001361190.2:n.729+10725C>G
NM_001374262.3:c.729+10725C>G NP_001361191.2:n.729+10725C>G
NM_001374263.2:c.832C>G NP_001361192.2:p.Arg278Gly
NM_001374264.2:c.832C>G NP_001361193.2:p.Arg278Gly
NM_005037.7:c.832C>G NP_005028.5:p.Arg278Gly
NM_138711.6:c.832C>G MANE Select NP_619725.3:p.Arg278Gly
NM_138712.5:c.832C>G NP_619726.3:p.Arg278Gly