Canonical Allele Identifier: CA1164245528
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078584G= , CM000663.2:g.40078584G= GRCh38
NC_000001.10:g.40544256G= , CM000663.1:g.40544256G= GRCh37
NC_000001.9:g.40316843G= NCBI36
NG_009192.1:g.23887C= , LRG_690:g.23887C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.699C= ENSP00000394863.4:p.Ser233=
ENST00000439754.6:c.702C= ENSP00000403207.2:p.Ser234=
ENST00000449045.7:c.393C= ENSP00000392293.2:p.Ser131=
ENST00000527311.7:c.471C= ENSP00000436695.3:p.Ser157=
ENST00000530076.6:c.45C= ENSP00000434007.1:p.Ser15=
ENST00000530704.6:c.*325C= ENSP00000431655.1:n.*325C=
ENST00000641083.1:c.680C=
ENST00000641236.1:n.939C=
ENST00000641319.1:c.702C= ENSP00000493128.1:p.Ser234=
ENST00000641381.1:c.149-1671C=
ENST00000641471.1:c.789C= ENSP00000493146.1:p.Ser263=
ENST00000641691.1:c.*554C= ENSP00000492910.1:n.*554C=
ENST00000641924.1:c.*131C= ENSP00000493063.1:n.*131C=
ENST00000642050.2:c.702C= MANE Select ENSP00000493153.1:p.Ser234=
ENST00000372775.2:n.99C=
ENST00000372779.8:c.789C= ENSP00000361865.4:p.Ser263=
ENST00000433473.7:c.702C= ENSP00000394863.3:p.Ser234=
ENST00000439754.5:c.387C= ENSP00000403207.1:p.Ser129=
ENST00000449045.6:c.393C= ENSP00000392293.2:p.Ser131=
ENST00000527311.6:c.477C= ENSP00000436695.2:p.Ser159=
ENST00000529905.5:c.702C= ENSP00000432053.1:p.Ser234=
ENST00000530076.5:c.45C= ENSP00000434007.1:p.Ser15=
ENST00000530704.5:c.*325C= ENSP00000431655.1:n.*325C=
NM_000310.3:c.702C= , LRG_690t1:c.702C= NP_000301.1:p.Ser234=
NM_001142604.1:c.393C= NP_001136076.1:p.Ser131=
XM_005271008.1:c.702C= XP_005271065.1:p.Ser234=
NM_001363695.1:c.702C= NP_001350624.1:p.Ser234=
NM_000310.4:c.702C= MANE Select NP_000301.1:p.Ser234=
NM_001142604.2:c.393C= NP_001136076.1:p.Ser131=
NM_001363695.2:c.702C= NP_001350624.1:p.Ser234=