Canonical Allele Identifier: CA1144228742

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074111G= , CM000663.2:g.40074111G=	GRCh38
NC_000001.10:g.40539783G= , CM000663.1:g.40539783G=	GRCh37
NC_000001.9:g.40312370G=	NCBI36
NG_009192.1:g.28360C= , LRG_690:g.28360C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.868C=	ENSP00000394863.4:p.Gln290=
ENST00000439754.6:c.799C=	ENSP00000403207.2:p.Gln267=
ENST00000449045.7:c.562C=	ENSP00000392293.2:p.Gln188=
ENST00000530076.6:c.214C=	ENSP00000434007.1:p.Gln72=
ENST00000530704.6:c.*494C=	ENSP00000431655.1:n.*494C=
ENST00000641083.1:c.961C=
ENST00000641236.1:n.1108C=
ENST00000641319.1:c.*81C=	ENSP00000493128.1:n.*81C=
ENST00000641381.1:c.293C=
ENST00000641471.1:c.958C=	ENSP00000493146.1:p.Gln320=
ENST00000641691.1:c.*723C=	ENSP00000492910.1:n.*723C=
ENST00000641924.1:c.*300C=	ENSP00000493063.1:n.*300C=
ENST00000642050.2:c.871C= MANE Select	ENSP00000493153.1:p.Gln291=
ENST00000372775.2:n.268C=
ENST00000433473.7:c.871C=	ENSP00000394863.3:p.Gln291=
ENST00000439754.5:c.484C=	ENSP00000403207.1:p.Gln162=
ENST00000449045.6:c.562C=	ENSP00000392293.2:p.Gln188=
ENST00000529905.5:c.871C=	ENSP00000432053.1:p.Gln291=
ENST00000530076.5:c.214C=	ENSP00000434007.1:p.Gln72=
ENST00000530704.5:c.*494C=	ENSP00000431655.1:n.*494C=
NM_000310.3:c.871C= , LRG_690t1:c.871C=	NP_000301.1:p.Gln291=
NM_001142604.1:c.562C=	NP_001136076.1:p.Gln188=
XM_005271008.1:c.799C=	XP_005271065.1:p.Gln267=
NM_001363695.1:c.799C=	NP_001350624.1:p.Gln267=
NM_000310.4:c.871C= MANE Select	NP_000301.1:p.Gln291=
NM_001142604.2:c.562C=	NP_001136076.1:p.Gln188=
NM_001363695.2:c.799C=	NP_001350624.1:p.Gln267=