Canonical Allele Identifier: CA918812078
Gene: TPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1564855391

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617068del , CM000673.2:g.6617068del GRCh38
NC_000011.9:g.6638299del , CM000673.1:g.6638299del GRCh37
NC_000011.8:g.6594875del NCBI36
NG_008653.1:g.7398del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.484del ENSP00000507321.1:p.Val162Ter
ENST00000299427.12:c.598del MANE Select ENSP00000299427.6:p.Val200Ter
ENST00000428886.7:n.833del
ENST00000436873.7:c.312+237del
ENST00000524788.2:n.1757del
ENST00000524903.2:n.1873del
ENST00000528807.2:n.254del
ENST00000530040.2:n.479+295del
ENST00000533371.6:c.-132del ENSP00000437066.1:n.-132del
ENST00000534644.6:n.546del
ENST00000642892.1:c.-132del ENSP00000494165.1:n.-132del
ENST00000643439.1:c.*338del ENSP00000495849.1:n.*338del
ENST00000643479.1:n.627del
ENST00000643516.1:c.395+237del
ENST00000644151.1:n.2037del
ENST00000644218.1:c.598del ENSP00000493574.1:p.Val200Ter
ENST00000644683.1:c.*51del ENSP00000494085.1:n.*51del
ENST00000644810.1:c.319del ENSP00000495895.1:p.Val107Ter
ENST00000644831.1:n.774del
ENST00000644933.1:c.-132del ENSP00000496133.1:n.-132del
ENST00000645020.1:n.1773del
ENST00000645285.1:c.-132del ENSP00000495058.1:n.-132del
ENST00000645331.1:n.964del
ENST00000645620.1:c.-132del ENSP00000493657.1:n.-132del
ENST00000646777.1:n.774del
ENST00000647016.1:n.1078del
ENST00000647152.1:c.-132del ENSP00000495893.1:n.-132del
ENST00000647209.1:c.*467del ENSP00000495558.1:n.*467del
ENST00000647346.1:n.1618del
ENST00000299427.10:c.598del ENSP00000299427.6:p.Val200Ter
ENST00000428886.6:n.767del
ENST00000436873.6:c.450+295del ENSP00000398136.2:n.450+295del
ENST00000524788.1:n.298del
ENST00000528571.5:c.*338del ENSP00000434647.1:n.*338del
ENST00000528807.1:n.148del
ENST00000533371.5:c.-132del ENSP00000437066.1:n.-132del
ENST00000534644.5:n.583del
ENST00000611494.4:c.598del ENSP00000484546.1:p.Val200Ter
NM_000391.3:c.598del NP_000382.3:p.Val200Ter
NM_000391.4:c.598del MANE Select NP_000382.3:p.Val200Ter