Canonical Allele Identifier: CA3771170

Gene: PPARD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35424010C>T , CM000668.2:g.35424010C>T	GRCh38
NC_000006.11:g.35391787C>T , CM000668.1:g.35391787C>T	GRCh37
NC_000006.10:g.35499765C>T	NCBI36
NG_012345.1:g.86453C>T
NG_012345.2:g.86453C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360694.8:c.489C>T MANE Select	ENSP00000353916.3:p.Asn163=
ENST00000311565.4:c.489C>T	ENSP00000310928.4:p.Asn163=
ENST00000337400.6:c.489C>T	ENSP00000337063.2:p.Asn163=
ENST00000360694.7:c.489C>T	ENSP00000353916.3:p.Asn163=
ENST00000418635.6:c.195C>T	ENSP00000413314.2:p.Asn65=
ENST00000448077.6:c.372C>T	ENSP00000414372.2:p.Asn124=
NM_001171818.1:c.489C>T	NP_001165289.1:p.Asn163=
NM_001171819.1:c.372C>T	NP_001165290.1:p.Asn124=
NM_001171820.1:c.195C>T	NP_001165291.1:p.Asn65=
NM_006238.4:c.489C>T	NP_006229.1:p.Asn163=
NM_177435.2:c.489C>T	NP_803184.1:p.Asn163=
XM_005249193.1:c.489C>T	XP_005249250.1:p.Asn163=
XM_006715120.1:c.489C>T	XP_006715183.1:p.Asn163=
XM_006715121.1:c.489C>T	XP_006715184.1:p.Asn163=
XM_006715123.1:c.489C>T	XP_006715186.1:p.Asn163=
XM_011514707.1:c.489C>T	XP_011513009.1:p.Asn163=
XM_011514708.1:c.489C>T	XP_011513010.1:p.Asn163=
XM_011514709.1:c.489C>T	XP_011513011.1:p.Asn163=
XM_011514710.1:c.489C>T	XP_011513012.1:p.Asn163=
XM_011514711.1:c.489C>T	XP_011513013.1:p.Asn163=
XM_011514712.1:c.489C>T	XP_011513014.1:p.Asn163=
XM_011514713.1:c.489C>T	XP_011513015.1:p.Asn163=
XM_017010972.1:c.489C>T	XP_016866461.1:p.Asn163=
XM_017010973.1:c.489C>T	XP_016866462.1:p.Asn163=
XM_017010974.1:c.489C>T	XP_016866463.1:p.Asn163=
XM_024446474.1:c.489C>T	XP_024302242.1:p.Asn163=
NM_006238.5:c.489C>T MANE Select	NP_006229.1:p.Asn163=
NM_001171818.2:c.489C>T	NP_001165289.1:p.Asn163=
NM_177435.3:c.489C>T	NP_803184.1:p.Asn163=
NM_001171819.2:c.372C>T	NP_001165290.1:p.Asn124=
NM_001171820.2:c.195C>T	NP_001165291.1:p.Asn65=