Canonical Allele Identifier: CA2408637492

Gene: PPARA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46218377C= , CM000684.2:g.46218377C=	GRCh38
NC_000022.10:g.46614274C= , CM000684.1:g.46614274C=	GRCh37
NC_000022.9:g.44992938C=	NCBI36
NG_012204.1:g.72776C=
NG_012204.2:g.72844C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005036.6:c.484C= MANE Select	NP_005027.2:p.Leu162=
ENST00000407236.6:c.484C= MANE Select	ENSP00000385523.1:p.Leu162=
NM_001001928.2:c.484C=	NP_001001928.1:p.Leu162=
NM_001001928.3:c.484C=	NP_001001928.1:p.Leu162=
NM_001001928.4:c.484C=	NP_001001928.1:p.Leu162=
NM_001001929.3:c.484C=	NP_001001929.1:p.Leu162=
NM_001362872.1:c.484C=	NP_001349801.1:p.Leu162=
NM_001362872.2:c.484C=	NP_001349801.1:p.Leu162=
NM_001362873.1:c.484C=	NP_001349802.1:p.Leu162=
NM_001362873.3:c.484C=	NP_001349802.1:p.Leu162=
NM_001393941.1:c.484C=	NP_001380870.1:p.Leu162=
NM_001393942.1:c.484C=	NP_001380871.1:p.Leu162=
NM_001393943.1:c.484C=	NP_001380872.1:p.Leu162=
NM_001393944.1:c.484C=	NP_001380873.1:p.Leu162=
NM_001393945.1:c.484C=	NP_001380874.1:p.Leu162=
NM_001393946.1:c.484C=	NP_001380875.1:p.Leu162=
NM_001393947.1:c.484C=	NP_001380876.1:p.Leu162=
NM_005036.4:c.484C=	NP_005027.2:p.Leu162=
NM_005036.5:c.484C=	NP_005027.2:p.Leu162=
ENST00000262735.9:c.484C=	ENSP00000262735.5:p.Leu162=
ENST00000402126.1:c.484C=	ENSP00000385246.1:p.Leu162=
ENST00000407236.5:c.484C=	ENSP00000385523.1:p.Leu162=
ENST00000493286.1:n.694C=
XM_005261655.2:c.484C=	XP_005261712.1:p.Leu162=
XM_005261656.2:c.484C=	XP_005261713.1:p.Leu162=
XM_005261656.3:c.484C=	XP_005261713.1:p.Leu162=
XM_006724269.2:c.484C=	XP_006724332.1:p.Leu162=
XM_006724270.2:c.484C=	XP_006724333.1:p.Leu162=
XM_006724270.3:c.484C=	XP_006724333.1:p.Leu162=
XM_011530239.1:c.484C=	XP_011528541.1:p.Leu162=
XM_011530239.2:c.484C=	XP_011528541.1:p.Leu162=
XM_011530240.1:c.484C=	XP_011528542.1:p.Leu162=
XM_011530240.2:c.484C=	XP_011528542.1:p.Leu162=
XM_011530241.1:c.484C=	XP_011528543.1:p.Leu162=
XM_011530241.2:c.484C=	XP_011528543.1:p.Leu162=
XM_011530242.1:c.484C=	XP_011528544.1:p.Leu162=
XM_011530242.2:c.484C=	XP_011528544.1:p.Leu162=
XM_011530243.1:c.484C=	XP_011528545.1:p.Leu162=
XM_011530243.2:c.484C=	XP_011528545.1:p.Leu162=
XM_011530244.1:c.78C=	XP_011528546.1:p.Ala26=
XM_011530244.2:c.78C=	XP_011528546.1:p.Ala26=
XM_011530245.1:c.78C=	XP_011528547.1:p.Ala26=
XM_011530245.2:c.78C=	XP_011528547.1:p.Ala26=
XM_017028839.1:c.78C=	XP_016884328.1:p.Ala26=
XM_024452252.1:c.78C=	XP_024308020.1:p.Ala26=
XM_024452253.1:c.78C=	XP_024308021.1:p.Ala26=
XR_001755253.1:n.802C=
XR_937869.1:n.799C=
XR_937869.2:n.802C=
XR_937870.1:n.798C=
XR_937870.2:n.802C=