Canonical Allele Identifier: CA1144228731

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091364A= , CM000663.2:g.40091364A=	GRCh38
NC_000001.10:g.40557036A= , CM000663.1:g.40557036A=	GRCh37
NC_000001.9:g.40329623A=	NCBI36
NG_009192.1:g.11107T= , LRG_690:g.11107T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*234T=	ENSP00000361865.5:n.*234T=
ENST00000433473.8:c.395T=	ENSP00000394863.4:p.Met132=
ENST00000439754.6:c.398T=	ENSP00000403207.2:p.Met133=
ENST00000449045.7:c.125-1852T=	ENSP00000392293.2:n.125-1852T=
ENST00000526547.2:c.678T=
ENST00000527311.7:c.270T=	ENSP00000436695.3:p.His90=
ENST00000530704.6:c.398T=	ENSP00000431655.1:p.Met133=
ENST00000641083.1:c.376T=
ENST00000641236.1:n.635T=
ENST00000641319.1:c.398T=	ENSP00000493128.1:p.Met133=
ENST00000641381.1:c.10T=
ENST00000641471.1:c.485T=	ENSP00000493146.1:p.Met162=
ENST00000641548.1:c.*250T=	ENSP00000492984.1:n.*250T=
ENST00000641691.1:c.*250T=	ENSP00000492910.1:n.*250T=
ENST00000641924.1:c.124+5751T=	ENSP00000493063.1:n.124+5751T=
ENST00000642050.2:c.398T= MANE Select	ENSP00000493153.1:p.Met133=
ENST00000372779.8:c.485T=	ENSP00000361865.4:p.Met162=
ENST00000433473.7:c.398T=	ENSP00000394863.3:p.Met133=
ENST00000439754.5:c.83T=	ENSP00000403207.1:p.Met28=
ENST00000449045.6:c.125-1852T=	ENSP00000392293.2:n.125-1852T=
ENST00000526547.1:c.248T=	ENSP00000436481.1:p.Met83=
ENST00000527311.6:c.173T=	ENSP00000436695.2:p.Met58=
ENST00000529905.5:c.398T=	ENSP00000432053.1:p.Met133=
ENST00000530704.5:c.398T=	ENSP00000431655.1:p.Met133=
NM_000310.3:c.398T= , LRG_690t1:c.398T=	NP_000301.1:p.Met133=
NM_001142604.1:c.125-1852T=	NP_001136076.1:n.125-1852T=
XM_005271008.1:c.398T=	XP_005271065.1:p.Met133=
NM_001363695.1:c.398T=	NP_001350624.1:p.Met133=
NM_000310.4:c.398T= MANE Select	NP_000301.1:p.Met133=
NM_001142604.2:c.125-1852T=	NP_001136076.1:n.125-1852T=
NM_001363695.2:c.398T=	NP_001350624.1:p.Met133=