Canonical Allele Identifier: CA1164245532
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078607T= , CM000663.2:g.40078607T= GRCh38
NC_000001.10:g.40544279T= , CM000663.1:g.40544279T= GRCh37
NC_000001.9:g.40316866T= NCBI36
NG_009192.1:g.23864A= , LRG_690:g.23864A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.676A= ENSP00000394863.4:p.Met226=
ENST00000439754.6:c.679A= ENSP00000403207.2:p.Met227=
ENST00000449045.7:c.370A= ENSP00000392293.2:p.Met124=
ENST00000527311.7:c.448A= ENSP00000436695.3:p.Met150=
ENST00000530076.6:c.22A= ENSP00000434007.1:p.Met8=
ENST00000530704.6:c.*302A= ENSP00000431655.1:n.*302A=
ENST00000641083.1:c.657A=
ENST00000641236.1:n.916A=
ENST00000641319.1:c.679A= ENSP00000493128.1:p.Met227=
ENST00000641381.1:c.149-1694A=
ENST00000641471.1:c.766A= ENSP00000493146.1:p.Met256=
ENST00000641691.1:c.*531A= ENSP00000492910.1:n.*531A=
ENST00000641924.1:c.*108A= ENSP00000493063.1:n.*108A=
ENST00000642050.2:c.679A= MANE Select ENSP00000493153.1:p.Met227=
ENST00000372775.2:n.76A=
ENST00000372779.8:c.766A= ENSP00000361865.4:p.Met256=
ENST00000433473.7:c.679A= ENSP00000394863.3:p.Met227=
ENST00000439754.5:c.364A= ENSP00000403207.1:p.Met122=
ENST00000449045.6:c.370A= ENSP00000392293.2:p.Met124=
ENST00000527311.6:c.454A= ENSP00000436695.2:p.Met152=
ENST00000529905.5:c.679A= ENSP00000432053.1:p.Met227=
ENST00000530076.5:c.22A= ENSP00000434007.1:p.Met8=
ENST00000530704.5:c.*302A= ENSP00000431655.1:n.*302A=
NM_000310.3:c.679A= , LRG_690t1:c.679A= NP_000301.1:p.Met227=
NM_001142604.1:c.370A= NP_001136076.1:p.Met124=
XM_005271008.1:c.679A= XP_005271065.1:p.Met227=
NM_001363695.1:c.679A= NP_001350624.1:p.Met227=
NM_000310.4:c.679A= MANE Select NP_000301.1:p.Met227=
NM_001142604.2:c.370A= NP_001136076.1:p.Met124=
NM_001363695.2:c.679A= NP_001350624.1:p.Met227=