Canonical Allele Identifier: CA20999345
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs945850854

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074273A>C , CM000663.2:g.40074273A>C GRCh38
NC_000001.10:g.40539945A>C , CM000663.1:g.40539945A>C GRCh37
NC_000001.9:g.40312532A>C NCBI36
NG_009192.1:g.28198T>G , LRG_690:g.28198T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.796-90T>G ENSP00000394863.4:n.796-90T>G
ENST00000439754.6:c.727-90T>G ENSP00000403207.2:n.727-90T>G
ENST00000449045.7:c.490-90T>G ENSP00000392293.2:n.490-90T>G
ENST00000527311.7:c.568-90T>G ENSP00000436695.3:n.568-90T>G
ENST00000530076.6:c.142-90T>G ENSP00000434007.1:n.142-90T>G
ENST00000530704.6:c.*422-90T>G ENSP00000431655.1:n.*422-90T>G
ENST00000641083.1:c.889-90T>G
ENST00000641236.1:n.1036-90T>G
ENST00000641319.1:c.*9-90T>G ENSP00000493128.1:n.*9-90T>G
ENST00000641381.1:c.221-90T>G
ENST00000641471.1:c.886-90T>G ENSP00000493146.1:n.886-90T>G
ENST00000641691.1:c.*651-90T>G ENSP00000492910.1:n.*651-90T>G
ENST00000641924.1:c.*228-90T>G ENSP00000493063.1:n.*228-90T>G
ENST00000642050.2:c.799-90T>G MANE Select ENSP00000493153.1:n.799-90T>G
ENST00000372775.2:n.196-90T>G
ENST00000433473.7:c.799-90T>G ENSP00000394863.3:n.799-90T>G
ENST00000439754.5:c.412-90T>G ENSP00000403207.1:n.412-90T>G
ENST00000449045.6:c.490-90T>G ENSP00000392293.2:n.490-90T>G
ENST00000527311.6:c.574-90T>G ENSP00000436695.2:n.574-90T>G
ENST00000529905.5:c.799-90T>G ENSP00000432053.1:n.799-90T>G
ENST00000530076.5:c.142-90T>G ENSP00000434007.1:n.142-90T>G
ENST00000530704.5:c.*422-90T>G ENSP00000431655.1:n.*422-90T>G
NM_000310.3:c.799-90T>G , LRG_690t1:c.799-90T>G NP_000301.1:n.799-90T>G
NM_001142604.1:c.490-90T>G NP_001136076.1:n.490-90T>G
XM_005271008.1:c.727-90T>G XP_005271065.1:n.727-90T>G
NM_001363695.1:c.727-90T>G NP_001350624.1:n.727-90T>G
NM_000310.4:c.799-90T>G MANE Select NP_000301.1:n.799-90T>G
NM_001142604.2:c.490-90T>G NP_001136076.1:n.490-90T>G
NM_001363695.2:c.727-90T>G NP_001350624.1:n.727-90T>G