Canonical Allele Identifier: CA1143646562
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40091329C= , CM000663.2:g.40091329C= GRCh38
NC_000001.10:g.40557001C= , CM000663.1:g.40557001C= GRCh37
NC_000001.9:g.40329588C= NCBI36
NG_009192.1:g.11142G= , LRG_690:g.11142G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.*269G= ENSP00000361865.5:n.*269G=
ENST00000433473.8:c.430G= ENSP00000394863.4:p.Gly144=
ENST00000439754.6:c.433G= ENSP00000403207.2:p.Gly145=
ENST00000449045.7:c.125-1817G= ENSP00000392293.2:n.125-1817G=
ENST00000526547.2:c.713G=
ENST00000527311.7:c.305G= ENSP00000436695.3:p.Ser102=
ENST00000530704.6:c.433G= ENSP00000431655.1:p.Val145=
ENST00000641083.1:c.411G=
ENST00000641236.1:n.670G=
ENST00000641319.1:c.433G= ENSP00000493128.1:p.Gly145=
ENST00000641381.1:c.45G=
ENST00000641471.1:c.520G= ENSP00000493146.1:p.Gly174=
ENST00000641548.1:c.*285G= ENSP00000492984.1:n.*285G=
ENST00000641691.1:c.*285G= ENSP00000492910.1:n.*285G=
ENST00000641924.1:c.124+5786G= ENSP00000493063.1:n.124+5786G=
ENST00000642050.2:c.433G= MANE Select ENSP00000493153.1:p.Gly145=
ENST00000372779.8:c.520G= ENSP00000361865.4:p.Gly174=
ENST00000433473.7:c.433G= ENSP00000394863.3:p.Gly145=
ENST00000439754.5:c.118G= ENSP00000403207.1:p.Gly40=
ENST00000449045.6:c.125-1817G= ENSP00000392293.2:n.125-1817G=
ENST00000526547.1:c.283G= ENSP00000436481.1:p.Gly95=
ENST00000527311.6:c.208G= ENSP00000436695.2:p.Gly70=
ENST00000529905.5:c.433G= ENSP00000432053.1:p.Gly145=
ENST00000530704.5:c.433G= ENSP00000431655.1:p.Val145=
NM_000310.3:c.433G= , LRG_690t1:c.433G= NP_000301.1:p.Gly145=
NM_001142604.1:c.125-1817G= NP_001136076.1:n.125-1817G=
XM_005271008.1:c.433G= XP_005271065.1:p.Gly145=
NM_001363695.1:c.433G= NP_001350624.1:p.Gly145=
NM_000310.4:c.433G= MANE Select NP_000301.1:p.Gly145=
NM_001142604.2:c.125-1817G= NP_001136076.1:n.125-1817G=
NM_001363695.2:c.433G= NP_001350624.1:p.Gly145=