Canonical Allele Identifier: CA1164243569
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074158T= , CM000663.2:g.40074158T= GRCh38
NC_000001.10:g.40539830T= , CM000663.1:g.40539830T= GRCh37
NC_000001.9:g.40312417T= NCBI36
NG_009192.1:g.28313A= , LRG_690:g.28313A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.821A= ENSP00000394863.4:p.Asp274=
ENST00000439754.6:c.752A= ENSP00000403207.2:p.Asp251=
ENST00000449045.7:c.515A= ENSP00000392293.2:p.Asp172=
ENST00000527311.7:c.593A= ENSP00000436695.3:p.Asp198=
ENST00000530076.6:c.167A= ENSP00000434007.1:p.Asp56=
ENST00000530704.6:c.*447A= ENSP00000431655.1:n.*447A=
ENST00000641083.1:c.914A=
ENST00000641236.1:n.1061A=
ENST00000641319.1:c.*34A= ENSP00000493128.1:n.*34A=
ENST00000641381.1:c.246A=
ENST00000641471.1:c.911A= ENSP00000493146.1:p.Asp304=
ENST00000641691.1:c.*676A= ENSP00000492910.1:n.*676A=
ENST00000641924.1:c.*253A= ENSP00000493063.1:n.*253A=
ENST00000642050.2:c.824A= MANE Select ENSP00000493153.1:p.Asp275=
ENST00000372775.2:n.221A=
ENST00000433473.7:c.824A= ENSP00000394863.3:p.Asp275=
ENST00000439754.5:c.437A= ENSP00000403207.1:p.Asp146=
ENST00000449045.6:c.515A= ENSP00000392293.2:p.Asp172=
ENST00000527311.6:c.599A= ENSP00000436695.2:p.Asp200=
ENST00000529905.5:c.824A= ENSP00000432053.1:p.Asp275=
ENST00000530076.5:c.167A= ENSP00000434007.1:p.Asp56=
ENST00000530704.5:c.*447A= ENSP00000431655.1:n.*447A=
NM_000310.3:c.824A= , LRG_690t1:c.824A= NP_000301.1:p.Asp275=
NM_001142604.1:c.515A= NP_001136076.1:p.Asp172=
XM_005271008.1:c.752A= XP_005271065.1:p.Asp251=
NM_001363695.1:c.752A= NP_001350624.1:p.Asp251=
NM_000310.4:c.824A= MANE Select NP_000301.1:p.Asp275=
NM_001142604.2:c.515A= NP_001136076.1:p.Asp172=
NM_001363695.2:c.752A= NP_001350624.1:p.Asp251=