Canonical Allele Identifier: CA1164243530

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074051T= , CM000663.2:g.40074051T=	GRCh38
NC_000001.10:g.40539723T= , CM000663.1:g.40539723T=	GRCh37
NC_000001.9:g.40312310T=	NCBI36
NG_009192.1:g.28420A= , LRG_690:g.28420A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.*10A=	ENSP00000394863.4:n.*10A=
ENST00000439754.6:c.*10A=	ENSP00000403207.2:n.*10A=
ENST00000449045.7:c.*10A=	ENSP00000392293.2:n.*10A=
ENST00000530076.6:c.*10A=	ENSP00000434007.1:n.*10A=
ENST00000530704.6:c.*554A=	ENSP00000431655.1:n.*554A=
ENST00000641083.1:c.1021A=
ENST00000641236.1:n.1168A=
ENST00000641319.1:c.*141A=	ENSP00000493128.1:n.*141A=
ENST00000641381.1:c.353A=
ENST00000641471.1:c.*10A=	ENSP00000493146.1:n.*10A=
ENST00000641691.1:c.*783A=	ENSP00000492910.1:n.*783A=
ENST00000641924.1:c.*360A=	ENSP00000493063.1:n.*360A=
ENST00000642050.2:c.*10A= MANE Select	ENSP00000493153.1:n.*10A=
ENST00000372775.2:n.328A=
ENST00000433473.7:c.*10A=	ENSP00000394863.3:n.*10A=
ENST00000439754.5:c.544A=	ENSP00000403207.1:n.544A=
ENST00000449045.6:c.*10A=	ENSP00000392293.2:n.*10A=
ENST00000529905.5:c.*10A=	ENSP00000432053.1:n.*10A=
ENST00000530076.5:c.*10A=	ENSP00000434007.1:n.*10A=
ENST00000530704.5:c.*554A=	ENSP00000431655.1:n.*554A=
NM_000310.3:c.*10A= , LRG_690t1:c.*10A=	NP_000301.1:n.*10A=
NM_001142604.1:c.*10A=	NP_001136076.1:n.*10A=
XM_005271008.1:c.*10A=	XP_005271065.1:n.*10A=
NM_001363695.1:c.*10A=	NP_001350624.1:n.*10A=
NM_000310.4:c.*10A= MANE Select	NP_000301.1:n.*10A=
NM_001142604.2:c.*10A=	NP_001136076.1:n.*10A=
NM_001363695.2:c.*10A=	NP_001350624.1:n.*10A=