Canonical Allele Identifier: CA1144144482
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080438G= , CM000663.2:g.40080438G= GRCh38
NC_000001.10:g.40546110G= , CM000663.1:g.40546110G= GRCh37
NC_000001.9:g.40318697G= NCBI36
NG_009192.1:g.22033C= , LRG_690:g.22033C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.583C= ENSP00000394863.4:p.Arg195=
ENST00000439754.6:c.586C= ENSP00000403207.2:p.Arg196=
ENST00000449045.7:c.277C= ENSP00000392293.2:p.Arg93=
ENST00000527311.7:c.355C= ENSP00000436695.3:p.Arg119=
ENST00000530076.6:c.-72C= ENSP00000434007.1:n.-72C=
ENST00000530704.6:c.*209C= ENSP00000431655.1:n.*209C=
ENST00000641083.1:c.564C=
ENST00000641236.1:n.823C=
ENST00000641319.1:c.586C= ENSP00000493128.1:p.Arg196=
ENST00000641381.1:c.149-3525C=
ENST00000641471.1:c.673C= ENSP00000493146.1:p.Arg225=
ENST00000641691.1:c.*438C= ENSP00000492910.1:n.*438C=
ENST00000641924.1:c.*15C= ENSP00000493063.1:n.*15C=
ENST00000642050.2:c.586C= MANE Select ENSP00000493153.1:p.Arg196=
ENST00000372779.8:c.673C= ENSP00000361865.4:p.Arg225=
ENST00000433473.7:c.586C= ENSP00000394863.3:p.Arg196=
ENST00000439754.5:c.271C= ENSP00000403207.1:p.Arg91=
ENST00000449045.6:c.277C= ENSP00000392293.2:p.Arg93=
ENST00000527311.6:c.361C= ENSP00000436695.2:p.Arg121=
ENST00000529905.5:c.586C= ENSP00000432053.1:p.Arg196=
ENST00000530076.5:c.-72C= ENSP00000434007.1:n.-72C=
ENST00000530704.5:c.*209C= ENSP00000431655.1:n.*209C=
NM_000310.3:c.586C= , LRG_690t1:c.586C= NP_000301.1:p.Arg196=
NM_001142604.1:c.277C= NP_001136076.1:p.Arg93=
XM_005271008.1:c.586C= XP_005271065.1:p.Arg196=
NM_001363695.1:c.586C= NP_001350624.1:p.Arg196=
NM_000310.4:c.586C= MANE Select NP_000301.1:p.Arg196=
NM_001142604.2:c.277C= NP_001136076.1:p.Arg93=
NM_001363695.2:c.586C= NP_001350624.1:p.Arg196=