Canonical Allele Identifier: CA1620878526
Gene: PPARD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35394748G= , CM000668.2:g.35394748G= GRCh38
NC_000006.11:g.35362525G= , CM000668.1:g.35362525G= GRCh37
NC_000006.10:g.35470503G= NCBI36
NG_012345.1:g.57191G=
NG_012345.2:g.57191G=

Transcript Alleles

HGVS Amino-acid Change
NM_006238.5:c.-101-16239G= MANE Select NP_006229.1:n.-101-16239G=
ENST00000360694.8:c.-101-16239G= MANE Select ENSP00000353916.3:n.-101-16239G=
NM_001171818.1:c.-197-2750G= NP_001165289.1:n.-197-2750G=
NM_001171818.2:c.-197-2750G= NP_001165289.1:n.-197-2750G=
NM_001171819.1:c.14-25379G= NP_001165290.1:n.14-25379G=
NM_001171819.2:c.14-25379G= NP_001165290.1:n.14-25379G=
NM_001171820.1:c.-101-16239G= NP_001165291.1:n.-101-16239G=
NM_001171820.2:c.-101-16239G= NP_001165291.1:n.-101-16239G=
NM_006238.4:c.-101-16239G= NP_006229.1:n.-101-16239G=
NM_177435.2:c.-101-16239G= NP_803184.1:n.-101-16239G=
NM_177435.3:c.-101-16239G= NP_803184.1:n.-101-16239G=
ENST00000311565.4:c.-197-2750G= ENSP00000310928.4:n.-197-2750G=
ENST00000337400.6:c.-197-2750G= ENSP00000337063.2:n.-197-2750G=
ENST00000360694.7:c.-101-16239G= ENSP00000353916.3:n.-101-16239G=
ENST00000418635.6:c.-101-16239G= ENSP00000413314.2:n.-101-16239G=
ENST00000448077.6:c.14-25379G= ENSP00000414372.2:n.14-25379G=
XM_005249193.1:c.-101-16239G= XP_005249250.1:n.-101-16239G=
XM_006715120.1:c.-101-16239G= XP_006715183.1:n.-101-16239G=
XM_006715121.1:c.-101-16239G= XP_006715184.1:n.-101-16239G=
XM_006715123.1:c.-101-16239G= XP_006715186.1:n.-101-16239G=
XM_011514707.1:c.-101-16239G= XP_011513009.1:n.-101-16239G=
XM_011514708.1:c.-101-16239G= XP_011513010.1:n.-101-16239G=
XM_011514709.1:c.-197-2750G= XP_011513011.1:n.-197-2750G=
XM_011514710.1:c.-101-16239G= XP_011513012.1:n.-101-16239G=
XM_011514711.1:c.-101-16239G= XP_011513013.1:n.-101-16239G=
XM_011514712.1:c.-101-16239G= XP_011513014.1:n.-101-16239G=
XM_011514713.1:c.-101-16239G= XP_011513015.1:n.-101-16239G=
XM_017010972.1:c.-250-15466G= XP_016866461.1:n.-250-15466G=
XM_017010973.1:c.-326-2229G= XP_016866462.1:n.-326-2229G=
XM_017010974.1:c.-101-16239G= XP_016866463.1:n.-101-16239G=