Canonical Allele Identifier: CA12442238

Gene: PPARD

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35411001C>T , CM000668.2:g.35411001C>T	GRCh38
NC_000006.11:g.35378778C>T , CM000668.1:g.35378778C>T	GRCh37
NC_000006.10:g.35486756C>T	NCBI36
NG_012345.1:g.73444C>T
NG_012345.2:g.73444C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360694.8:c.-87C>T MANE Select	ENSP00000353916.3:n.-87C>T
ENST00000311565.4:c.-87C>T	ENSP00000310928.4:n.-87C>T
ENST00000337400.6:c.-87C>T	ENSP00000337063.2:n.-87C>T
ENST00000360694.7:c.-87C>T	ENSP00000353916.3:n.-87C>T
ENST00000418635.6:c.-87C>T	ENSP00000413314.2:n.-87C>T
ENST00000448077.6:c.14-9126C>T	ENSP00000414372.2:n.14-9126C>T
NM_001171818.1:c.-87C>T	NP_001165289.1:n.-87C>T
NM_001171819.1:c.14-9126C>T	NP_001165290.1:n.14-9126C>T
NM_001171820.1:c.-87C>T	NP_001165291.1:n.-87C>T
NM_006238.4:c.-87C>T	NP_006229.1:n.-87C>T
NM_177435.2:c.-87C>T	NP_803184.1:n.-87C>T
XM_005249193.1:c.-87C>T	XP_005249250.1:n.-87C>T
XM_006715120.1:c.-87C>T	XP_006715183.1:n.-87C>T
XM_006715121.1:c.-87C>T	XP_006715184.1:n.-87C>T
XM_006715123.1:c.-87C>T	XP_006715186.1:n.-87C>T
XM_011514707.1:c.-87C>T	XP_011513009.1:n.-87C>T
XM_011514708.1:c.-87C>T	XP_011513010.1:n.-87C>T
XM_011514709.1:c.-87C>T	XP_011513011.1:n.-87C>T
XM_011514710.1:c.-87C>T	XP_011513012.1:n.-87C>T
XM_011514711.1:c.-87C>T	XP_011513013.1:n.-87C>T
XM_011514712.1:c.-87C>T	XP_011513014.1:n.-87C>T
XM_011514713.1:c.-87C>T	XP_011513015.1:n.-87C>T
XM_017010972.1:c.-87C>T	XP_016866461.1:n.-87C>T
XM_017010973.1:c.-87C>T	XP_016866462.1:n.-87C>T
XM_017010974.1:c.-87C>T	XP_016866463.1:n.-87C>T
NM_006238.5:c.-87C>T MANE Select	NP_006229.1:n.-87C>T
NM_001171818.2:c.-87C>T	NP_001165289.1:n.-87C>T
NM_177435.3:c.-87C>T	NP_803184.1:n.-87C>T
NM_001171819.2:c.14-9126C>T	NP_001165290.1:n.14-9126C>T
NM_001171820.2:c.-87C>T	NP_001165291.1:n.-87C>T