Canonical Allele Identifier: CA1164243558

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074132C= , CM000663.2:g.40074132C=	GRCh38
NC_000001.10:g.40539804C= , CM000663.1:g.40539804C=	GRCh37
NC_000001.9:g.40312391C=	NCBI36
NG_009192.1:g.28339G= , LRG_690:g.28339G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.847G=	ENSP00000394863.4:p.Ala283=
ENST00000439754.6:c.778G=	ENSP00000403207.2:p.Ala260=
ENST00000449045.7:c.541G=	ENSP00000392293.2:p.Ala181=
ENST00000527311.7:c.619G=	ENSP00000436695.3:p.Ala207=
ENST00000530076.6:c.193G=	ENSP00000434007.1:p.Ala65=
ENST00000530704.6:c.*473G=	ENSP00000431655.1:n.*473G=
ENST00000641083.1:c.940G=
ENST00000641236.1:n.1087G=
ENST00000641319.1:c.*60G=	ENSP00000493128.1:n.*60G=
ENST00000641381.1:c.272G=
ENST00000641471.1:c.937G=	ENSP00000493146.1:p.Ala313=
ENST00000641691.1:c.*702G=	ENSP00000492910.1:n.*702G=
ENST00000641924.1:c.*279G=	ENSP00000493063.1:n.*279G=
ENST00000642050.2:c.850G= MANE Select	ENSP00000493153.1:p.Ala284=
ENST00000372775.2:n.247G=
ENST00000433473.7:c.850G=	ENSP00000394863.3:p.Ala284=
ENST00000439754.5:c.463G=	ENSP00000403207.1:p.Ala155=
ENST00000449045.6:c.541G=	ENSP00000392293.2:p.Ala181=
ENST00000529905.5:c.850G=	ENSP00000432053.1:p.Ala284=
ENST00000530076.5:c.193G=	ENSP00000434007.1:p.Ala65=
ENST00000530704.5:c.*473G=	ENSP00000431655.1:n.*473G=
NM_000310.3:c.850G= , LRG_690t1:c.850G=	NP_000301.1:p.Ala284=
NM_001142604.1:c.541G=	NP_001136076.1:p.Ala181=
XM_005271008.1:c.778G=	XP_005271065.1:p.Ala260=
NM_001363695.1:c.778G=	NP_001350624.1:p.Ala260=
NM_000310.4:c.850G= MANE Select	NP_000301.1:p.Ala284=
NM_001142604.2:c.541G=	NP_001136076.1:p.Ala181=
NM_001363695.2:c.778G=	NP_001350624.1:p.Ala260=