Canonical Allele Identifier: CA1144228730

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091349G= , CM000663.2:g.40091349G=	GRCh38
NC_000001.10:g.40557021G= , CM000663.1:g.40557021G=	GRCh37
NC_000001.9:g.40329608G=	NCBI36
NG_009192.1:g.11122C= , LRG_690:g.11122C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372779.9:c.*249C=	ENSP00000361865.5:n.*249C=
ENST00000433473.8:c.410C=	ENSP00000394863.4:p.Ser137=
ENST00000439754.6:c.413C=	ENSP00000403207.2:p.Ser138=
ENST00000449045.7:c.125-1837C=	ENSP00000392293.2:n.125-1837C=
ENST00000526547.2:c.693C=
ENST00000527311.7:c.285C=	ENSP00000436695.3:p.Leu95=
ENST00000530704.6:c.413C=	ENSP00000431655.1:p.Ser138=
ENST00000641083.1:c.391C=
ENST00000641236.1:n.650C=
ENST00000641319.1:c.413C=	ENSP00000493128.1:p.Ser138=
ENST00000641381.1:c.25C=
ENST00000641471.1:c.500C=	ENSP00000493146.1:p.Ser167=
ENST00000641548.1:c.*265C=	ENSP00000492984.1:n.*265C=
ENST00000641691.1:c.*265C=	ENSP00000492910.1:n.*265C=
ENST00000641924.1:c.124+5766C=	ENSP00000493063.1:n.124+5766C=
ENST00000642050.2:c.413C= MANE Select	ENSP00000493153.1:p.Ser138=
ENST00000372779.8:c.500C=	ENSP00000361865.4:p.Ser167=
ENST00000433473.7:c.413C=	ENSP00000394863.3:p.Ser138=
ENST00000439754.5:c.98C=	ENSP00000403207.1:p.Ser33=
ENST00000449045.6:c.125-1837C=	ENSP00000392293.2:n.125-1837C=
ENST00000526547.1:c.263C=	ENSP00000436481.1:p.Ser88=
ENST00000527311.6:c.188C=	ENSP00000436695.2:p.Ser63=
ENST00000529905.5:c.413C=	ENSP00000432053.1:p.Ser138=
ENST00000530704.5:c.413C=	ENSP00000431655.1:p.Ser138=
NM_000310.3:c.413C= , LRG_690t1:c.413C=	NP_000301.1:p.Ser138=
NM_001142604.1:c.125-1837C=	NP_001136076.1:n.125-1837C=
XM_005271008.1:c.413C=	XP_005271065.1:p.Ser138=
NM_001363695.1:c.413C=	NP_001350624.1:p.Ser138=
NM_000310.4:c.413C= MANE Select	NP_000301.1:p.Ser138=
NM_001142604.2:c.125-1837C=	NP_001136076.1:n.125-1837C=
NM_001363695.2:c.413C=	NP_001350624.1:p.Ser138=