Canonical Allele Identifier: CA1164243552

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074118G= , CM000663.2:g.40074118G=	GRCh38
NC_000001.10:g.40539790G= , CM000663.1:g.40539790G=	GRCh37
NC_000001.9:g.40312377G=	NCBI36
NG_009192.1:g.28353C= , LRG_690:g.28353C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.861C=	ENSP00000394863.4:p.Asp287=
ENST00000439754.6:c.792C=	ENSP00000403207.2:p.Asp264=
ENST00000449045.7:c.555C=	ENSP00000392293.2:p.Asp185=
ENST00000530076.6:c.207C=	ENSP00000434007.1:p.Asp69=
ENST00000530704.6:c.*487C=	ENSP00000431655.1:n.*487C=
ENST00000641083.1:c.954C=
ENST00000641236.1:n.1101C=
ENST00000641319.1:c.*74C=	ENSP00000493128.1:n.*74C=
ENST00000641381.1:c.286C=
ENST00000641471.1:c.951C=	ENSP00000493146.1:p.Asp317=
ENST00000641691.1:c.*716C=	ENSP00000492910.1:n.*716C=
ENST00000641924.1:c.*293C=	ENSP00000493063.1:n.*293C=
ENST00000642050.2:c.864C= MANE Select	ENSP00000493153.1:p.Asp288=
ENST00000372775.2:n.261C=
ENST00000433473.7:c.864C=	ENSP00000394863.3:p.Asp288=
ENST00000439754.5:c.477C=	ENSP00000403207.1:p.Asp159=
ENST00000449045.6:c.555C=	ENSP00000392293.2:p.Asp185=
ENST00000529905.5:c.864C=	ENSP00000432053.1:p.Asp288=
ENST00000530076.5:c.207C=	ENSP00000434007.1:p.Asp69=
ENST00000530704.5:c.*487C=	ENSP00000431655.1:n.*487C=
NM_000310.3:c.864C= , LRG_690t1:c.864C=	NP_000301.1:p.Asp288=
NM_001142604.1:c.555C=	NP_001136076.1:p.Asp185=
XM_005271008.1:c.792C=	XP_005271065.1:p.Asp264=
NM_001363695.1:c.792C=	NP_001350624.1:p.Asp264=
NM_000310.4:c.864C= MANE Select	NP_000301.1:p.Asp288=
NM_001142604.2:c.555C=	NP_001136076.1:p.Asp185=
NM_001363695.2:c.792C=	NP_001350624.1:p.Asp264=