Canonical Allele Identifier: CA1164252274
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092125T= , CM000663.2:g.40092125T= GRCh38
NC_000001.10:g.40557797T= , CM000663.1:g.40557797T= GRCh37
NC_000001.9:g.40330384T= NCBI36
NG_009192.1:g.10346A= , LRG_690:g.10346A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.*118A= ENSP00000361865.5:n.*118A=
ENST00000433473.8:c.279A= ENSP00000394863.4:p.Thr93=
ENST00000439754.6:c.282A= ENSP00000403207.2:p.Thr94=
ENST00000449045.7:c.125-2613A= ENSP00000392293.2:n.125-2613A=
ENST00000526547.2:c.562A=
ENST00000527311.7:c.234+273A= ENSP00000436695.3:n.234+273A=
ENST00000530704.6:c.282A= ENSP00000431655.1:p.Thr94=
ENST00000641083.1:c.260A=
ENST00000641236.1:n.519A=
ENST00000641319.1:c.282A= ENSP00000493128.1:p.Thr94=
ENST00000641471.1:c.369A= ENSP00000493146.1:p.Thr123=
ENST00000641548.1:c.*134A= ENSP00000492984.1:n.*134A=
ENST00000641691.1:c.*134A= ENSP00000492910.1:n.*134A=
ENST00000641924.1:c.124+4990A= ENSP00000493063.1:n.124+4990A=
ENST00000642050.2:c.282A= MANE Select ENSP00000493153.1:p.Thr94=
ENST00000372779.8:c.369A= ENSP00000361865.4:p.Thr123=
ENST00000433473.7:c.282A= ENSP00000394863.3:p.Thr94=
ENST00000449045.6:c.125-2613A= ENSP00000392293.2:n.125-2613A=
ENST00000526547.1:c.132A= ENSP00000436481.1:p.Thr44=
ENST00000527311.6:c.125-68A= ENSP00000436695.2:n.125-68A=
ENST00000529905.5:c.282A= ENSP00000432053.1:p.Thr94=
ENST00000530704.5:c.282A= ENSP00000431655.1:p.Thr94=
NM_000310.3:c.282A= , LRG_690t1:c.282A= NP_000301.1:p.Thr94=
NM_001142604.1:c.125-2613A= NP_001136076.1:n.125-2613A=
XM_005271008.1:c.282A= XP_005271065.1:p.Thr94=
NM_001363695.1:c.282A= NP_001350624.1:p.Thr94=
NM_000310.4:c.282A= MANE Select NP_000301.1:p.Thr94=
NM_001142604.2:c.125-2613A= NP_001136076.1:n.125-2613A=
NM_001363695.2:c.282A= NP_001350624.1:p.Thr94=