Canonical Allele Identifier: CA1620894118

Gene: PPARD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35427740_35427742delinsCTG , CM000668.2:g.35427740_35427742delinsCTG	GRCh38
NC_000006.11:g.35395517_35395519delinsCTG , CM000668.1:g.35395517_35395519delinsCTG	GRCh37
NC_000006.10:g.35503495_35503497delinsCTG	NCBI36
NG_012345.1:g.90183_90185delinsCTG
NG_012345.2:g.90183_90185delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000360694.8:c.*1661_*1663delinsCTG MANE Select	ENSP00000353916.3:n.*1661_*1663delinsCTG
ENST00000311565.4:c.*1661_*1663delinsCTG	ENSP00000310928.4:n.*1661_*1663delinsCTG
ENST00000360694.7:c.*1661_*1663delinsCTG	ENSP00000353916.3:n.*1661_*1663delinsCTG
ENST00000418635.6:c.*1661_*1663delinsCTG	ENSP00000413314.2:n.*1661_*1663delinsCTG
ENST00000448077.6:c.*1661_*1663delinsCTG	ENSP00000414372.2:n.*1661_*1663delinsCTG
NM_001171818.1:c.*1661_*1663delinsCTG	NP_001165289.1:n.*1661_*1663delinsCTG
NM_001171819.1:c.*1661_*1663delinsCTG	NP_001165290.1:n.*1661_*1663delinsCTG
NM_001171820.1:c.*1661_*1663delinsCTG	NP_001165291.1:n.*1661_*1663delinsCTG
NM_006238.4:c.*1661_*1663delinsCTG	NP_006229.1:n.*1661_*1663delinsCTG
XM_005249193.1:c.*1661_*1663delinsCTG	XP_005249250.1:n.*1661_*1663delinsCTG
XM_006715120.1:c.*1661_*1663delinsCTG	XP_006715183.1:n.*1661_*1663delinsCTG
XM_006715121.1:c.*1661_*1663delinsCTG	XP_006715184.1:n.*1661_*1663delinsCTG
XM_006715123.1:c.*1661_*1663delinsCTG	XP_006715186.1:n.*1661_*1663delinsCTG
XM_011514707.1:c.*1661_*1663delinsCTG	XP_011513009.1:n.*1661_*1663delinsCTG
XM_011514708.1:c.*1661_*1663delinsCTG	XP_011513010.1:n.*1661_*1663delinsCTG
XM_011514709.1:c.*1661_*1663delinsCTG	XP_011513011.1:n.*1661_*1663delinsCTG
XM_011514710.1:c.*1661_*1663delinsCTG	XP_011513012.1:n.*1661_*1663delinsCTG
XM_011514711.1:c.*1661_*1663delinsCTG	XP_011513013.1:n.*1661_*1663delinsCTG
XM_011514712.1:c.*1661_*1663delinsCTG	XP_011513014.1:n.*1661_*1663delinsCTG
XM_011514713.1:c.*1773_*1775delinsCTG	XP_011513015.1:n.*1773_*1775delinsCTG
XM_017010972.1:c.*1661_*1663delinsCTG	XP_016866461.1:n.*1661_*1663delinsCTG
XM_017010973.1:c.*1661_*1663delinsCTG	XP_016866462.1:n.*1661_*1663delinsCTG
XM_017010974.1:c.*1661_*1663delinsCTG	XP_016866463.1:n.*1661_*1663delinsCTG
XM_024446474.1:c.*1773_*1775delinsCTG	XP_024302242.1:n.*1773_*1775delinsCTG
NM_006238.5:c.*1661_*1663delinsCTG MANE Select	NP_006229.1:n.*1661_*1663delinsCTG
NM_001171818.2:c.*1661_*1663delinsCTG	NP_001165289.1:n.*1661_*1663delinsCTG
NM_001171819.2:c.*1661_*1663delinsCTG	NP_001165290.1:n.*1661_*1663delinsCTG
NM_001171820.2:c.*1661_*1663delinsCTG	NP_001165291.1:n.*1661_*1663delinsCTG