Canonical Allele Identifier: CA1164252106

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092046G= , CM000663.2:g.40092046G=	GRCh38
NC_000001.10:g.40557718G= , CM000663.1:g.40557718G=	GRCh37
NC_000001.9:g.40330305G=	NCBI36
NG_009192.1:g.10425C= , LRG_690:g.10425C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*197C=	ENSP00000361865.5:n.*197C=
ENST00000433473.8:c.358C=	ENSP00000394863.4:p.Leu120=
ENST00000439754.6:c.361C=	ENSP00000403207.2:p.Leu121=
ENST00000449045.7:c.125-2534C=	ENSP00000392293.2:n.125-2534C=
ENST00000526547.2:c.641C=
ENST00000527311.7:c.234+352C=	ENSP00000436695.3:n.234+352C=
ENST00000530704.6:c.361C=	ENSP00000431655.1:p.Leu121=
ENST00000641083.1:c.339C=
ENST00000641236.1:n.598C=
ENST00000641319.1:c.361C=	ENSP00000493128.1:p.Leu121=
ENST00000641471.1:c.448C=	ENSP00000493146.1:p.Leu150=
ENST00000641548.1:c.*213C=	ENSP00000492984.1:n.*213C=
ENST00000641691.1:c.*213C=	ENSP00000492910.1:n.*213C=
ENST00000641924.1:c.124+5069C=	ENSP00000493063.1:n.124+5069C=
ENST00000642050.2:c.361C= MANE Select	ENSP00000493153.1:p.Leu121=
ENST00000372779.8:c.448C=	ENSP00000361865.4:p.Leu150=
ENST00000433473.7:c.361C=	ENSP00000394863.3:p.Leu121=
ENST00000439754.5:c.46C=	ENSP00000403207.1:p.Leu16=
ENST00000449045.6:c.125-2534C=	ENSP00000392293.2:n.125-2534C=
ENST00000526547.1:c.211C=	ENSP00000436481.1:p.Leu71=
ENST00000527311.6:c.136C=	ENSP00000436695.2:p.Leu46=
ENST00000529905.5:c.361C=	ENSP00000432053.1:p.Leu121=
ENST00000530704.5:c.361C=	ENSP00000431655.1:p.Leu121=
NM_000310.3:c.361C= , LRG_690t1:c.361C=	NP_000301.1:p.Leu121=
NM_001142604.1:c.125-2534C=	NP_001136076.1:n.125-2534C=
XM_005271008.1:c.361C=	XP_005271065.1:p.Leu121=
NM_001363695.1:c.361C=	NP_001350624.1:p.Leu121=
NM_000310.4:c.361C= MANE Select	NP_000301.1:p.Leu121=
NM_001142604.2:c.125-2534C=	NP_001136076.1:n.125-2534C=
NM_001363695.2:c.361C=	NP_001350624.1:p.Leu121=