Canonical Allele Identifier: CA1143470593
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080398C= , CM000663.2:g.40080398C= GRCh38
NC_000001.10:g.40546070C= , CM000663.1:g.40546070C= GRCh37
NC_000001.9:g.40318657C= NCBI36
NG_009192.1:g.22073G= , LRG_690:g.22073G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.623G= ENSP00000394863.4:p.Arg208=
ENST00000439754.6:c.626G= ENSP00000403207.2:p.Arg209=
ENST00000449045.7:c.317G= ENSP00000392293.2:p.Arg106=
ENST00000527311.7:c.395G= ENSP00000436695.3:p.Arg132=
ENST00000530076.6:c.-32G= ENSP00000434007.1:n.-32G=
ENST00000530704.6:c.*249G= ENSP00000431655.1:n.*249G=
ENST00000641083.1:c.604G=
ENST00000641236.1:n.863G=
ENST00000641319.1:c.626G= ENSP00000493128.1:p.Arg209=
ENST00000641381.1:c.149-3485G=
ENST00000641471.1:c.713G= ENSP00000493146.1:p.Arg238=
ENST00000641691.1:c.*478G= ENSP00000492910.1:n.*478G=
ENST00000641924.1:c.*55G= ENSP00000493063.1:n.*55G=
ENST00000642050.2:c.626G= MANE Select ENSP00000493153.1:p.Arg209=
ENST00000372779.8:c.713G= ENSP00000361865.4:p.Arg238=
ENST00000433473.7:c.626G= ENSP00000394863.3:p.Arg209=
ENST00000439754.5:c.311G= ENSP00000403207.1:p.Arg104=
ENST00000449045.6:c.317G= ENSP00000392293.2:p.Arg106=
ENST00000527311.6:c.401G= ENSP00000436695.2:p.Arg134=
ENST00000529905.5:c.626G= ENSP00000432053.1:p.Arg209=
ENST00000530076.5:c.-32G= ENSP00000434007.1:n.-32G=
ENST00000530704.5:c.*249G= ENSP00000431655.1:n.*249G=
NM_000310.3:c.626G= , LRG_690t1:c.626G= NP_000301.1:p.Arg209=
NM_001142604.1:c.317G= NP_001136076.1:p.Arg106=
XM_005271008.1:c.626G= XP_005271065.1:p.Arg209=
NM_001363695.1:c.626G= NP_001350624.1:p.Arg209=
NM_000310.4:c.626G= MANE Select NP_000301.1:p.Arg209=
NM_001142604.2:c.317G= NP_001136076.1:p.Arg106=
NM_001363695.2:c.626G= NP_001350624.1:p.Arg209=