Canonical Allele Identifier: CA566486300

Gene: PPARD

Linked Data

• dbSNP Id: rs1453781266
• gnomAD v2: 6-35349939-GTGGGAAGCTC-G
• gnomAD v3: 6-35382162-GTGGGAAGCTC-G
• gnomAD v4: 6-35382162-GTGGGAAGCTC-G
• MyVariant Identifiers: chr6:g.35349940_35349949del (hg19) ; chr6:g.35382163_35382172del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35382168_35382177del , CM000668.2:g.35382168_35382177del	GRCh38
NC_000006.11:g.35349945_35349954del , CM000668.1:g.35349945_35349954del	GRCh37
NC_000006.10:g.35457923_35457932del	NCBI36
NG_012345.1:g.44611_44620del
NG_012345.2:g.44611_44620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360694.8:c.-101-28819_-101-28810del MANE Select	ENSP00000353916.3:n.-101-28819_-101-28810del
ENST00000311565.4:c.-197-15330_-197-15321del	ENSP00000310928.4:n.-197-15330_-197-15321del
ENST00000337400.6:c.-197-15330_-197-15321del	ENSP00000337063.2:n.-197-15330_-197-15321del
ENST00000360694.7:c.-101-28819_-101-28810del	ENSP00000353916.3:n.-101-28819_-101-28810del
ENST00000418635.6:c.-101-28819_-101-28810del	ENSP00000413314.2:n.-101-28819_-101-28810del
ENST00000448077.6:c.13+35018_13+35027del	ENSP00000414372.2:n.13+35018_13+35027del
NM_001171818.1:c.-197-15330_-197-15321del	NP_001165289.1:n.-197-15330_-197-15321del
NM_001171819.1:c.13+35018_13+35027del	NP_001165290.1:n.13+35018_13+35027del
NM_001171820.1:c.-101-28819_-101-28810del	NP_001165291.1:n.-101-28819_-101-28810del
NM_006238.4:c.-101-28819_-101-28810del	NP_006229.1:n.-101-28819_-101-28810del
NM_177435.2:c.-101-28819_-101-28810del	NP_803184.1:n.-101-28819_-101-28810del
XM_005249193.1:c.-101-28819_-101-28810del	XP_005249250.1:n.-101-28819_-101-28810del
XM_006715120.1:c.-101-28819_-101-28810del	XP_006715183.1:n.-101-28819_-101-28810del
XM_006715121.1:c.-101-28819_-101-28810del	XP_006715184.1:n.-101-28819_-101-28810del
XM_006715123.1:c.-101-28819_-101-28810del	XP_006715186.1:n.-101-28819_-101-28810del
XM_011514707.1:c.-101-28819_-101-28810del	XP_011513009.1:n.-101-28819_-101-28810del
XM_011514708.1:c.-101-28819_-101-28810del	XP_011513010.1:n.-101-28819_-101-28810del
XM_011514709.1:c.-197-15330_-197-15321del	XP_011513011.1:n.-197-15330_-197-15321del
XM_011514710.1:c.-101-28819_-101-28810del	XP_011513012.1:n.-101-28819_-101-28810del
XM_011514711.1:c.-101-28819_-101-28810del	XP_011513013.1:n.-101-28819_-101-28810del
XM_011514712.1:c.-101-28819_-101-28810del	XP_011513014.1:n.-101-28819_-101-28810del
XM_011514713.1:c.-101-28819_-101-28810del	XP_011513015.1:n.-101-28819_-101-28810del
XM_017010972.1:c.-250-28046_-250-28037del	XP_016866461.1:n.-250-28046_-250-28037del
XM_017010973.1:c.-326-14809_-326-14800del	XP_016866462.1:n.-326-14809_-326-14800del
XM_017010974.1:c.-101-28819_-101-28810del	XP_016866463.1:n.-101-28819_-101-28810del
NM_006238.5:c.-101-28819_-101-28810del MANE Select	NP_006229.1:n.-101-28819_-101-28810del
NM_001171818.2:c.-197-15330_-197-15321del	NP_001165289.1:n.-197-15330_-197-15321del
NM_177435.3:c.-101-28819_-101-28810del	NP_803184.1:n.-101-28819_-101-28810del
NM_001171819.2:c.13+35018_13+35027del	NP_001165290.1:n.13+35018_13+35027del
NM_001171820.2:c.-101-28819_-101-28810del	NP_001165291.1:n.-101-28819_-101-28810del