Canonical Allele Identifier: CA1164252665
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092399T= , CM000663.2:g.40092399T= GRCh38
NC_000001.10:g.40558071T= , CM000663.1:g.40558071T= GRCh37
NC_000001.9:g.40330658T= NCBI36
NG_009192.1:g.10072A= , LRG_690:g.10072A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.*69A= ENSP00000361865.5:n.*69A=
ENST00000433473.8:c.230A= ENSP00000394863.4:p.Glu77=
ENST00000439754.6:c.233A= ENSP00000403207.2:p.Glu78=
ENST00000449045.7:c.125-2887A= ENSP00000392293.2:n.125-2887A=
ENST00000526547.2:c.513A=
ENST00000527311.7:c.233A= ENSP00000436695.3:p.Glu78=
ENST00000530704.6:c.233A= ENSP00000431655.1:p.Glu78=
ENST00000641083.1:c.211A=
ENST00000641236.1:n.245A=
ENST00000641319.1:c.233A= ENSP00000493128.1:p.Glu78=
ENST00000641471.1:c.320A= ENSP00000493146.1:p.Glu107=
ENST00000641548.1:c.*85A= ENSP00000492984.1:n.*85A=
ENST00000641691.1:c.*85A= ENSP00000492910.1:n.*85A=
ENST00000641924.1:c.124+4716A= ENSP00000493063.1:n.124+4716A=
ENST00000642050.2:c.233A= MANE Select ENSP00000493153.1:p.Glu78=
ENST00000372779.8:c.320A= ENSP00000361865.4:p.Glu107=
ENST00000433473.7:c.233A= ENSP00000394863.3:p.Glu78=
ENST00000449045.6:c.125-2887A= ENSP00000392293.2:n.125-2887A=
ENST00000526547.1:c.83A= ENSP00000436481.1:p.Glu28=
ENST00000527311.6:c.125-342A= ENSP00000436695.2:n.125-342A=
ENST00000529905.5:c.233A= ENSP00000432053.1:p.Glu78=
ENST00000530704.5:c.233A= ENSP00000431655.1:p.Glu78=
NM_000310.3:c.233A= , LRG_690t1:c.233A= NP_000301.1:p.Glu78=
NM_001142604.1:c.125-2887A= NP_001136076.1:n.125-2887A=
XM_005271008.1:c.233A= XP_005271065.1:p.Glu78=
NM_001363695.1:c.233A= NP_001350624.1:p.Glu78=
NM_000310.4:c.233A= MANE Select NP_000301.1:p.Glu78=
NM_001142604.2:c.125-2887A= NP_001136076.1:n.125-2887A=
NM_001363695.2:c.233A= NP_001350624.1:p.Glu78=