Canonical Allele Identifier: CA1164252810
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092482G= , CM000663.2:g.40092482G= GRCh38
NC_000001.10:g.40558154G= , CM000663.1:g.40558154G= GRCh37
NC_000001.9:g.40330741G= NCBI36
NG_009192.1:g.9989C= , LRG_690:g.9989C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.154C= ENSP00000361865.5:p.His52=
ENST00000433473.8:c.147C= ENSP00000394863.4:p.Ser49=
ENST00000439754.6:c.150C= ENSP00000403207.2:p.Ser50=
ENST00000449045.7:c.125-2970C= ENSP00000392293.2:n.125-2970C=
ENST00000526547.2:c.430C=
ENST00000527311.7:c.150C= ENSP00000436695.3:p.Ser50=
ENST00000530704.6:c.150C= ENSP00000431655.1:p.Ser50=
ENST00000641083.1:c.128C=
ENST00000641236.1:n.162C=
ENST00000641319.1:c.150C= ENSP00000493128.1:p.Ser50=
ENST00000641471.1:c.237C= ENSP00000493146.1:p.Ser79=
ENST00000641548.1:c.*2C= ENSP00000492984.1:n.*2C=
ENST00000641691.1:c.*2C= ENSP00000492910.1:n.*2C=
ENST00000641924.1:c.124+4633C= ENSP00000493063.1:n.124+4633C=
ENST00000642050.2:c.150C= MANE Select ENSP00000493153.1:p.Ser50=
ENST00000372779.8:c.237C= ENSP00000361865.4:p.Ser79=
ENST00000433473.7:c.150C= ENSP00000394863.3:p.Ser50=
ENST00000449045.6:c.125-2970C= ENSP00000392293.2:n.125-2970C=
ENST00000526547.1:c.-1C= ENSP00000436481.1:n.-1C=
ENST00000527311.6:c.125-425C= ENSP00000436695.2:n.125-425C=
ENST00000529905.5:c.150C= ENSP00000432053.1:p.Ser50=
ENST00000530704.5:c.150C= ENSP00000431655.1:p.Ser50=
NM_000310.3:c.150C= , LRG_690t1:c.150C= NP_000301.1:p.Ser50=
NM_001142604.1:c.125-2970C= NP_001136076.1:n.125-2970C=
XM_005271008.1:c.150C= XP_005271065.1:p.Ser50=
NM_001363695.1:c.150C= NP_001350624.1:p.Ser50=
NM_000310.4:c.150C= MANE Select NP_000301.1:p.Ser50=
NM_001142604.2:c.125-2970C= NP_001136076.1:n.125-2970C=
NM_001363695.2:c.150C= NP_001350624.1:p.Ser50=