Canonical Allele Identifier: CA1164235696
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080433G= , CM000663.2:g.40080433G= GRCh38
NC_000001.10:g.40546105G= , CM000663.1:g.40546105G= GRCh37
NC_000001.9:g.40318692G= NCBI36
NG_009192.1:g.22038C= , LRG_690:g.22038C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.588C= ENSP00000394863.4:p.Asn196=
ENST00000439754.6:c.591C= ENSP00000403207.2:p.Asn197=
ENST00000449045.7:c.282C= ENSP00000392293.2:p.Asn94=
ENST00000527311.7:c.360C= ENSP00000436695.3:p.Asn120=
ENST00000530076.6:c.-67C= ENSP00000434007.1:n.-67C=
ENST00000530704.6:c.*214C= ENSP00000431655.1:n.*214C=
ENST00000641083.1:c.569C=
ENST00000641236.1:n.828C=
ENST00000641319.1:c.591C= ENSP00000493128.1:p.Asn197=
ENST00000641381.1:c.149-3520C=
ENST00000641471.1:c.678C= ENSP00000493146.1:p.Asn226=
ENST00000641691.1:c.*443C= ENSP00000492910.1:n.*443C=
ENST00000641924.1:c.*20C= ENSP00000493063.1:n.*20C=
ENST00000642050.2:c.591C= MANE Select ENSP00000493153.1:p.Asn197=
ENST00000372779.8:c.678C= ENSP00000361865.4:p.Asn226=
ENST00000433473.7:c.591C= ENSP00000394863.3:p.Asn197=
ENST00000439754.5:c.276C= ENSP00000403207.1:p.Asn92=
ENST00000449045.6:c.282C= ENSP00000392293.2:p.Asn94=
ENST00000527311.6:c.366C= ENSP00000436695.2:p.Asn122=
ENST00000529905.5:c.591C= ENSP00000432053.1:p.Asn197=
ENST00000530076.5:c.-67C= ENSP00000434007.1:n.-67C=
ENST00000530704.5:c.*214C= ENSP00000431655.1:n.*214C=
NM_000310.3:c.591C= , LRG_690t1:c.591C= NP_000301.1:p.Asn197=
NM_001142604.1:c.282C= NP_001136076.1:p.Asn94=
XM_005271008.1:c.591C= XP_005271065.1:p.Asn197=
NM_001363695.1:c.591C= NP_001350624.1:p.Asn197=
NM_000310.4:c.591C= MANE Select NP_000301.1:p.Asn197=
NM_001142604.2:c.282C= NP_001136076.1:p.Asn94=
NM_001363695.2:c.591C= NP_001350624.1:p.Asn197=