Canonical Allele Identifier: CA1164235756
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080452T= , CM000663.2:g.40080452T= GRCh38
NC_000001.10:g.40546124T= , CM000663.1:g.40546124T= GRCh37
NC_000001.9:g.40318711T= NCBI36
NG_009192.1:g.22019A= , LRG_690:g.22019A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.*408A= ENSP00000361865.5:n.*408A=
ENST00000433473.8:c.569A= ENSP00000394863.4:p.Lys190=
ENST00000439754.6:c.572A= ENSP00000403207.2:p.Lys191=
ENST00000449045.7:c.263A= ENSP00000392293.2:p.Lys88=
ENST00000527311.7:c.341A= ENSP00000436695.3:p.Lys114=
ENST00000530076.6:c.-86A= ENSP00000434007.1:n.-86A=
ENST00000530704.6:c.*195A= ENSP00000431655.1:n.*195A=
ENST00000641083.1:c.550A=
ENST00000641236.1:n.809A=
ENST00000641319.1:c.572A= ENSP00000493128.1:p.Lys191=
ENST00000641381.1:c.149-3539A=
ENST00000641471.1:c.659A= ENSP00000493146.1:p.Lys220=
ENST00000641691.1:c.*424A= ENSP00000492910.1:n.*424A=
ENST00000641924.1:c.*1A= ENSP00000493063.1:n.*1A=
ENST00000642050.2:c.572A= MANE Select ENSP00000493153.1:p.Lys191=
ENST00000372779.8:c.659A= ENSP00000361865.4:p.Lys220=
ENST00000433473.7:c.572A= ENSP00000394863.3:p.Lys191=
ENST00000439754.5:c.257A= ENSP00000403207.1:p.Lys86=
ENST00000449045.6:c.263A= ENSP00000392293.2:p.Lys88=
ENST00000527311.6:c.347A= ENSP00000436695.2:p.Lys116=
ENST00000529905.5:c.572A= ENSP00000432053.1:p.Lys191=
ENST00000530076.5:c.-86A= ENSP00000434007.1:n.-86A=
ENST00000530704.5:c.*195A= ENSP00000431655.1:n.*195A=
NM_000310.3:c.572A= , LRG_690t1:c.572A= NP_000301.1:p.Lys191=
NM_001142604.1:c.263A= NP_001136076.1:p.Lys88=
XM_005271008.1:c.572A= XP_005271065.1:p.Lys191=
NM_001363695.1:c.572A= NP_001350624.1:p.Lys191=
NM_000310.4:c.572A= MANE Select NP_000301.1:p.Lys191=
NM_001142604.2:c.263A= NP_001136076.1:p.Lys88=
NM_001363695.2:c.572A= NP_001350624.1:p.Lys191=