Canonical Allele Identifier: CA1164243563
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074147G= , CM000663.2:g.40074147G= GRCh38
NC_000001.10:g.40539819G= , CM000663.1:g.40539819G= GRCh37
NC_000001.9:g.40312406G= NCBI36
NG_009192.1:g.28324C= , LRG_690:g.28324C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.832C= ENSP00000394863.4:p.Gln278=
ENST00000439754.6:c.763C= ENSP00000403207.2:p.Gln255=
ENST00000449045.7:c.526C= ENSP00000392293.2:p.Gln176=
ENST00000527311.7:c.604C= ENSP00000436695.3:p.Gln202=
ENST00000530076.6:c.178C= ENSP00000434007.1:p.Gln60=
ENST00000530704.6:c.*458C= ENSP00000431655.1:n.*458C=
ENST00000641083.1:c.925C=
ENST00000641236.1:n.1072C=
ENST00000641319.1:c.*45C= ENSP00000493128.1:n.*45C=
ENST00000641381.1:c.257C=
ENST00000641471.1:c.922C= ENSP00000493146.1:p.Gln308=
ENST00000641691.1:c.*687C= ENSP00000492910.1:n.*687C=
ENST00000641924.1:c.*264C= ENSP00000493063.1:n.*264C=
ENST00000642050.2:c.835C= MANE Select ENSP00000493153.1:p.Gln279=
ENST00000372775.2:n.232C=
ENST00000433473.7:c.835C= ENSP00000394863.3:p.Gln279=
ENST00000439754.5:c.448C= ENSP00000403207.1:p.Gln150=
ENST00000449045.6:c.526C= ENSP00000392293.2:p.Gln176=
ENST00000527311.6:c.610C= ENSP00000436695.2:p.Gln204=
ENST00000529905.5:c.835C= ENSP00000432053.1:p.Gln279=
ENST00000530076.5:c.178C= ENSP00000434007.1:p.Gln60=
ENST00000530704.5:c.*458C= ENSP00000431655.1:n.*458C=
NM_000310.3:c.835C= , LRG_690t1:c.835C= NP_000301.1:p.Gln279=
NM_001142604.1:c.526C= NP_001136076.1:p.Gln176=
XM_005271008.1:c.763C= XP_005271065.1:p.Gln255=
NM_001363695.1:c.763C= NP_001350624.1:p.Gln255=
NM_000310.4:c.835C= MANE Select NP_000301.1:p.Gln279=
NM_001142604.2:c.526C= NP_001136076.1:p.Gln176=
NM_001363695.2:c.763C= NP_001350624.1:p.Gln255=