Canonical Allele Identifier: CA1087818448

Gene: PPARD

Linked Data

• gnomAD v3: 6-35385646-T-TAAAAAAAAA
• gnomAD v4: 6-35385646-T-TAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35385659_35385667dup , CM000668.2:g.35385659_35385667dup	GRCh38
NC_000006.11:g.35353436_35353444dup , CM000668.1:g.35353436_35353444dup	GRCh37
NC_000006.10:g.35461414_35461422dup	NCBI36
NG_012345.1:g.48102_48110dup
NG_012345.2:g.48102_48110dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360694.8:c.-101-25328_-101-25320dup MANE Select	ENSP00000353916.3:n.-101-25328_-101-25320dup
ENST00000311565.4:c.-197-11839_-197-11831dup	ENSP00000310928.4:n.-197-11839_-197-11831dup
ENST00000337400.6:c.-197-11839_-197-11831dup	ENSP00000337063.2:n.-197-11839_-197-11831dup
ENST00000360694.7:c.-101-25328_-101-25320dup	ENSP00000353916.3:n.-101-25328_-101-25320dup
ENST00000418635.6:c.-101-25328_-101-25320dup	ENSP00000413314.2:n.-101-25328_-101-25320dup
ENST00000448077.6:c.14-34468_14-34460dup	ENSP00000414372.2:n.14-34468_14-34460dup
NM_001171818.1:c.-197-11839_-197-11831dup	NP_001165289.1:n.-197-11839_-197-11831dup
NM_001171819.1:c.14-34468_14-34460dup	NP_001165290.1:n.14-34468_14-34460dup
NM_001171820.1:c.-101-25328_-101-25320dup	NP_001165291.1:n.-101-25328_-101-25320dup
NM_006238.4:c.-101-25328_-101-25320dup	NP_006229.1:n.-101-25328_-101-25320dup
NM_177435.2:c.-101-25328_-101-25320dup	NP_803184.1:n.-101-25328_-101-25320dup
XM_005249193.1:c.-101-25328_-101-25320dup	XP_005249250.1:n.-101-25328_-101-25320dup
XM_006715120.1:c.-101-25328_-101-25320dup	XP_006715183.1:n.-101-25328_-101-25320dup
XM_006715121.1:c.-101-25328_-101-25320dup	XP_006715184.1:n.-101-25328_-101-25320dup
XM_006715123.1:c.-101-25328_-101-25320dup	XP_006715186.1:n.-101-25328_-101-25320dup
XM_011514707.1:c.-101-25328_-101-25320dup	XP_011513009.1:n.-101-25328_-101-25320dup
XM_011514708.1:c.-101-25328_-101-25320dup	XP_011513010.1:n.-101-25328_-101-25320dup
XM_011514709.1:c.-197-11839_-197-11831dup	XP_011513011.1:n.-197-11839_-197-11831dup
XM_011514710.1:c.-101-25328_-101-25320dup	XP_011513012.1:n.-101-25328_-101-25320dup
XM_011514711.1:c.-101-25328_-101-25320dup	XP_011513013.1:n.-101-25328_-101-25320dup
XM_011514712.1:c.-101-25328_-101-25320dup	XP_011513014.1:n.-101-25328_-101-25320dup
XM_011514713.1:c.-101-25328_-101-25320dup	XP_011513015.1:n.-101-25328_-101-25320dup
XM_017010972.1:c.-250-24555_-250-24547dup	XP_016866461.1:n.-250-24555_-250-24547dup
XM_017010973.1:c.-326-11318_-326-11310dup	XP_016866462.1:n.-326-11318_-326-11310dup
XM_017010974.1:c.-101-25328_-101-25320dup	XP_016866463.1:n.-101-25328_-101-25320dup
NM_006238.5:c.-101-25328_-101-25320dup MANE Select	NP_006229.1:n.-101-25328_-101-25320dup
NM_001171818.2:c.-197-11839_-197-11831dup	NP_001165289.1:n.-197-11839_-197-11831dup
NM_177435.3:c.-101-25328_-101-25320dup	NP_803184.1:n.-101-25328_-101-25320dup
NM_001171819.2:c.14-34468_14-34460dup	NP_001165290.1:n.14-34468_14-34460dup
NM_001171820.2:c.-101-25328_-101-25320dup	NP_001165291.1:n.-101-25328_-101-25320dup