Canonical Allele Identifier: CA339849766
Gene: PPT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092436A>C , CM000663.2:g.40092436A>C GRCh38
NC_000001.10:g.40558108A>C , CM000663.1:g.40558108A>C GRCh37
NC_000001.9:g.40330695A>C NCBI36
NG_009192.1:g.10035T>G , LRG_690:g.10035T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.*32T>G ENSP00000361865.5:n.*32T>G
ENST00000433473.8:c.193T>G ENSP00000394863.4:p.Tyr65Asp
ENST00000439754.6:c.196T>G ENSP00000403207.2:p.Tyr66Asp
ENST00000449045.7:c.125-2924T>G ENSP00000392293.2:n.125-2924T>G
ENST00000526547.2:c.476T>G
ENST00000527311.7:c.196T>G ENSP00000436695.3:p.Tyr66Asp
ENST00000530704.6:c.196T>G ENSP00000431655.1:p.Tyr66Asp
ENST00000641083.1:c.174T>G
ENST00000641236.1:n.208T>G
ENST00000641319.1:c.196T>G ENSP00000493128.1:p.Tyr66Asp
ENST00000641471.1:c.283T>G ENSP00000493146.1:p.Tyr95Asp
ENST00000641548.1:c.*48T>G ENSP00000492984.1:n.*48T>G
ENST00000641691.1:c.*48T>G ENSP00000492910.1:n.*48T>G
ENST00000641924.1:c.124+4679T>G ENSP00000493063.1:n.124+4679T>G
ENST00000642050.2:c.196T>G MANE Select ENSP00000493153.1:p.Tyr66Asp
ENST00000372779.8:c.283T>G ENSP00000361865.4:p.Tyr95Asp
ENST00000433473.7:c.196T>G ENSP00000394863.3:p.Tyr66Asp
ENST00000449045.6:c.125-2924T>G ENSP00000392293.2:n.125-2924T>G
ENST00000526547.1:c.46T>G ENSP00000436481.1:p.Tyr16Asp
ENST00000527311.6:c.125-379T>G ENSP00000436695.2:n.125-379T>G
ENST00000529905.5:c.196T>G ENSP00000432053.1:p.Tyr66Asp
ENST00000530704.5:c.196T>G ENSP00000431655.1:p.Tyr66Asp
NM_000310.3:c.196T>G , LRG_690t1:c.196T>G NP_000301.1:p.Tyr66Asp
NM_001142604.1:c.125-2924T>G NP_001136076.1:n.125-2924T>G
XM_005271008.1:c.196T>G XP_005271065.1:p.Tyr66Asp
NM_001363695.1:c.196T>G NP_001350624.1:p.Tyr66Asp
NM_000310.4:c.196T>G MANE Select NP_000301.1:p.Tyr66Asp
NM_001142604.2:c.125-2924T>G NP_001136076.1:n.125-2924T>G
NM_001363695.2:c.196T>G NP_001350624.1:p.Tyr66Asp