Canonical Allele Identifier: CA1164243566
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074152G= , CM000663.2:g.40074152G= GRCh38
NC_000001.10:g.40539824G= , CM000663.1:g.40539824G= GRCh37
NC_000001.9:g.40312411G= NCBI36
NG_009192.1:g.28319C= , LRG_690:g.28319C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.827C= ENSP00000394863.4:p.Ala276=
ENST00000439754.6:c.758C= ENSP00000403207.2:p.Ala253=
ENST00000449045.7:c.521C= ENSP00000392293.2:p.Ala174=
ENST00000527311.7:c.599C= ENSP00000436695.3:p.Ala200=
ENST00000530076.6:c.173C= ENSP00000434007.1:p.Ala58=
ENST00000530704.6:c.*453C= ENSP00000431655.1:n.*453C=
ENST00000641083.1:c.920C=
ENST00000641236.1:n.1067C=
ENST00000641319.1:c.*40C= ENSP00000493128.1:n.*40C=
ENST00000641381.1:c.252C=
ENST00000641471.1:c.917C= ENSP00000493146.1:p.Ala306=
ENST00000641691.1:c.*682C= ENSP00000492910.1:n.*682C=
ENST00000641924.1:c.*259C= ENSP00000493063.1:n.*259C=
ENST00000642050.2:c.830C= MANE Select ENSP00000493153.1:p.Ala277=
ENST00000372775.2:n.227C=
ENST00000433473.7:c.830C= ENSP00000394863.3:p.Ala277=
ENST00000439754.5:c.443C= ENSP00000403207.1:p.Ala148=
ENST00000449045.6:c.521C= ENSP00000392293.2:p.Ala174=
ENST00000527311.6:c.605C= ENSP00000436695.2:p.Ala202=
ENST00000529905.5:c.830C= ENSP00000432053.1:p.Ala277=
ENST00000530076.5:c.173C= ENSP00000434007.1:p.Ala58=
ENST00000530704.5:c.*453C= ENSP00000431655.1:n.*453C=
NM_000310.3:c.830C= , LRG_690t1:c.830C= NP_000301.1:p.Ala277=
NM_001142604.1:c.521C= NP_001136076.1:p.Ala174=
XM_005271008.1:c.758C= XP_005271065.1:p.Ala253=
NM_001363695.1:c.758C= NP_001350624.1:p.Ala253=
NM_000310.4:c.830C= MANE Select NP_000301.1:p.Ala277=
NM_001142604.2:c.521C= NP_001136076.1:p.Ala174=
NM_001363695.2:c.758C= NP_001350624.1:p.Ala253=