Canonical Allele Identifier: CA1144228756
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092522A= , CM000663.2:g.40092522A= GRCh38
NC_000001.10:g.40558194A= , CM000663.1:g.40558194A= GRCh37
NC_000001.9:g.40330781A= NCBI36
NG_009192.1:g.9949T= , LRG_690:g.9949T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.129-15T= ENSP00000361865.5:n.129-15T=
ENST00000433473.8:c.125-18T= ENSP00000394863.4:n.125-18T=
ENST00000439754.6:c.125-15T= ENSP00000403207.2:n.125-15T=
ENST00000449045.7:c.125-3010T= ENSP00000392293.2:n.125-3010T=
ENST00000526547.2:c.405-15T=
ENST00000527311.7:c.125-15T= ENSP00000436695.3:n.125-15T=
ENST00000530704.6:c.125-15T= ENSP00000431655.1:n.125-15T=
ENST00000641083.1:c.103-15T=
ENST00000641236.1:n.137-15T=
ENST00000641319.1:c.125-15T= ENSP00000493128.1:n.125-15T=
ENST00000641471.1:c.212-15T= ENSP00000493146.1:n.212-15T=
ENST00000641548.1:c.125-22T= ENSP00000492984.1:n.125-22T=
ENST00000641691.1:c.125-22T= ENSP00000492910.1:n.125-22T=
ENST00000641924.1:c.124+4593T= ENSP00000493063.1:n.124+4593T=
ENST00000642050.2:c.125-15T= MANE Select ENSP00000493153.1:n.125-15T=
ENST00000372779.8:c.212-15T= ENSP00000361865.4:n.212-15T=
ENST00000433473.7:c.125-15T= ENSP00000394863.3:n.125-15T=
ENST00000449045.6:c.125-3010T= ENSP00000392293.2:n.125-3010T=
ENST00000526547.1:c.-26-15T= ENSP00000436481.1:n.-26-15T=
ENST00000527311.6:c.125-465T= ENSP00000436695.2:n.125-465T=
ENST00000529905.5:c.125-15T= ENSP00000432053.1:n.125-15T=
ENST00000530704.5:c.125-15T= ENSP00000431655.1:n.125-15T=
NM_000310.3:c.125-15T= , LRG_690t1:c.125-15T= NP_000301.1:n.125-15T=
NM_001142604.1:c.125-3010T= NP_001136076.1:n.125-3010T=
XM_005271008.1:c.125-15T= XP_005271065.1:n.125-15T=
NM_001363695.1:c.125-15T= NP_001350624.1:n.125-15T=
NM_000310.4:c.125-15T= MANE Select NP_000301.1:n.125-15T=
NM_001142604.2:c.125-3010T= NP_001136076.1:n.125-3010T=
NM_001363695.2:c.125-15T= NP_001350624.1:n.125-15T=