Canonical Allele Identifier: CA934783019
Gene: TPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1855549253

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6614723del , CM000673.2:g.6614723del GRCh38
NC_000011.9:g.6635954del , CM000673.1:g.6635954del GRCh37
NC_000011.8:g.6592530del NCBI36
NG_008653.1:g.9739del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.1438-37del ENSP00000507321.1:n.1438-37del
ENST00000299427.12:c.1552-37del MANE Select ENSP00000299427.6:n.1552-37del
ENST00000524611.2:n.554del
ENST00000524924.2:n.672-37del
ENST00000533371.6:c.823-37del ENSP00000437066.1:n.823-37del
ENST00000642892.1:c.823-37del ENSP00000494165.1:n.823-37del
ENST00000643342.1:c.625-37del
ENST00000643439.1:c.*1292-37del ENSP00000495849.1:n.*1292-37del
ENST00000643479.1:n.1738-37del
ENST00000643516.1:c.1061-37del
ENST00000644218.1:c.1363-37del ENSP00000493574.1:n.1363-37del
ENST00000644683.1:c.*1005-37del ENSP00000494085.1:n.*1005-37del
ENST00000644810.1:c.1273-37del ENSP00000495895.1:n.1273-37del
ENST00000644831.1:n.1728-37del
ENST00000644933.1:c.*418-37del ENSP00000496133.1:n.*418-37del
ENST00000645285.1:c.*418-37del ENSP00000495058.1:n.*418-37del
ENST00000645331.1:n.2757-37del
ENST00000645620.1:c.823-37del ENSP00000493657.1:n.823-37del
ENST00000646691.1:n.1439-37del
ENST00000646777.1:n.1885-37del
ENST00000647016.1:n.2032-37del
ENST00000647152.1:c.823-37del ENSP00000495893.1:n.823-37del
ENST00000647209.1:c.*1421-37del ENSP00000495558.1:n.*1421-37del
ENST00000647346.1:n.2572-37del
ENST00000299427.10:c.1552-37del ENSP00000299427.6:n.1552-37del
ENST00000524611.1:n.430-37del
ENST00000533371.5:c.823-37del ENSP00000437066.1:n.823-37del
ENST00000611494.4:c.1552-37del ENSP00000484546.1:n.1552-37del
NM_000391.3:c.1552-37del NP_000382.3:n.1552-37del
NM_000391.4:c.1552-37del MANE Select NP_000382.3:n.1552-37del