Canonical Allele Identifier: CA1141935028
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080440T= , CM000663.2:g.40080440T= GRCh38
NC_000001.10:g.40546112T= , CM000663.1:g.40546112T= GRCh37
NC_000001.9:g.40318699T= NCBI36
NG_009192.1:g.22031A= , LRG_690:g.22031A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.581A= ENSP00000394863.4:p.Tyr194=
ENST00000439754.6:c.584A= ENSP00000403207.2:p.Tyr195=
ENST00000449045.7:c.275A= ENSP00000392293.2:p.Tyr92=
ENST00000527311.7:c.353A= ENSP00000436695.3:p.Tyr118=
ENST00000530076.6:c.-74A= ENSP00000434007.1:n.-74A=
ENST00000530704.6:c.*207A= ENSP00000431655.1:n.*207A=
ENST00000641083.1:c.562A=
ENST00000641236.1:n.821A=
ENST00000641319.1:c.584A= ENSP00000493128.1:p.Tyr195=
ENST00000641381.1:c.149-3527A=
ENST00000641471.1:c.671A= ENSP00000493146.1:p.Tyr224=
ENST00000641691.1:c.*436A= ENSP00000492910.1:n.*436A=
ENST00000641924.1:c.*13A= ENSP00000493063.1:n.*13A=
ENST00000642050.2:c.584A= MANE Select ENSP00000493153.1:p.Tyr195=
ENST00000372779.8:c.671A= ENSP00000361865.4:p.Tyr224=
ENST00000433473.7:c.584A= ENSP00000394863.3:p.Tyr195=
ENST00000439754.5:c.269A= ENSP00000403207.1:p.Tyr90=
ENST00000449045.6:c.275A= ENSP00000392293.2:p.Tyr92=
ENST00000527311.6:c.359A= ENSP00000436695.2:p.Tyr120=
ENST00000529905.5:c.584A= ENSP00000432053.1:p.Tyr195=
ENST00000530076.5:c.-74A= ENSP00000434007.1:n.-74A=
ENST00000530704.5:c.*207A= ENSP00000431655.1:n.*207A=
NM_000310.3:c.584A= , LRG_690t1:c.584A= NP_000301.1:p.Tyr195=
NM_001142604.1:c.275A= NP_001136076.1:p.Tyr92=
XM_005271008.1:c.584A= XP_005271065.1:p.Tyr195=
NM_001363695.1:c.584A= NP_001350624.1:p.Tyr195=
NM_000310.4:c.584A= MANE Select NP_000301.1:p.Tyr195=
NM_001142604.2:c.275A= NP_001136076.1:p.Tyr92=
NM_001363695.2:c.584A= NP_001350624.1:p.Tyr195=