Canonical Allele Identifier: CA1164245546
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078647C= , CM000663.2:g.40078647C= GRCh38
NC_000001.10:g.40544319C= , CM000663.1:g.40544319C= GRCh37
NC_000001.9:g.40316906C= NCBI36
NG_009192.1:g.23824G= , LRG_690:g.23824G=

Transcript Alleles

HGVS Amino-acid change
ENST00000433473.8:c.636G= ENSP00000394863.4:p.Glu212=
ENST00000439754.6:c.639G= ENSP00000403207.2:p.Glu213=
ENST00000449045.7:c.330G= ENSP00000392293.2:p.Glu110=
ENST00000527311.7:c.408G= ENSP00000436695.3:p.Glu136=
ENST00000530076.6:c.-19G= ENSP00000434007.1:n.-19G=
ENST00000530704.6:c.*262G= ENSP00000431655.1:n.*262G=
ENST00000641083.1:c.617G=
ENST00000641236.1:n.876G=
ENST00000641319.1:c.639G= ENSP00000493128.1:p.Glu213=
ENST00000641381.1:c.149-1734G=
ENST00000641471.1:c.726G= ENSP00000493146.1:p.Glu242=
ENST00000641691.1:c.*491G= ENSP00000492910.1:n.*491G=
ENST00000641924.1:c.*68G= ENSP00000493063.1:n.*68G=
ENST00000642050.2:c.639G= MANE Select ENSP00000493153.1:p.Glu213=
ENST00000372775.2:n.36G=
ENST00000372779.8:c.726G= ENSP00000361865.4:p.Glu242=
ENST00000433473.7:c.639G= ENSP00000394863.3:p.Glu213=
ENST00000439754.5:c.324G= ENSP00000403207.1:p.Glu108=
ENST00000449045.6:c.330G= ENSP00000392293.2:p.Glu110=
ENST00000527311.6:c.414G= ENSP00000436695.2:p.Glu138=
ENST00000529905.5:c.639G= ENSP00000432053.1:p.Glu213=
ENST00000530076.5:c.-19G= ENSP00000434007.1:n.-19G=
ENST00000530704.5:c.*262G= ENSP00000431655.1:n.*262G=
NM_000310.3:c.639G= , LRG_690t1:c.639G= NP_000301.1:p.Glu213=
NM_001142604.1:c.330G= NP_001136076.1:p.Glu110=
XM_005271008.1:c.639G= XP_005271065.1:p.Glu213=
NM_001363695.1:c.639G= NP_001350624.1:p.Glu213=
NM_000310.4:c.639G= MANE Select NP_000301.1:p.Glu213=
NM_001142604.2:c.330G= NP_001136076.1:p.Glu110=
NM_001363695.2:c.639G= NP_001350624.1:p.Glu213=