Canonical Allele Identifier: CA912972915
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6615366_6615386del , CM000673.2:g.6615366_6615386del GRCh38
NC_000011.9:g.6636597_6636617del , CM000673.1:g.6636597_6636617del GRCh37
NC_000011.8:g.6593173_6593193del NCBI36
NG_008653.1:g.9077_9097del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.1153-56_1153-36del ENSP00000507321.1:n.1153-56_1153-36del
ENST00000299427.12:c.1267-56_1267-36del MANE Select ENSP00000299427.6:n.1267-56_1267-36del
ENST00000436873.7:c.504-56_504-36del
ENST00000524611.2:n.71_91del
ENST00000524924.2:n.387-56_387-36del
ENST00000533371.6:c.538-56_538-36del ENSP00000437066.1:n.538-56_538-36del
ENST00000642892.1:c.538-56_538-36del ENSP00000494165.1:n.538-56_538-36del
ENST00000643342.1:c.340-56_340-36del
ENST00000643439.1:c.*1007-56_*1007-36del ENSP00000495849.1:n.*1007-56_*1007-36del
ENST00000643479.1:n.1453-56_1453-36del
ENST00000643516.1:c.776-56_776-36del
ENST00000644218.1:c.1078-56_1078-36del ENSP00000493574.1:n.1078-56_1078-36del
ENST00000644683.1:c.*720-56_*720-36del ENSP00000494085.1:n.*720-56_*720-36del
ENST00000644810.1:c.988-56_988-36del ENSP00000495895.1:n.988-56_988-36del
ENST00000644831.1:n.1443-56_1443-36del
ENST00000644933.1:c.*133-56_*133-36del ENSP00000496133.1:n.*133-56_*133-36del
ENST00000645285.1:c.*133-56_*133-36del ENSP00000495058.1:n.*133-56_*133-36del
ENST00000645331.1:n.2472-56_2472-36del
ENST00000645620.1:c.538-56_538-36del ENSP00000493657.1:n.538-56_538-36del
ENST00000646691.1:n.1098_1118del
ENST00000646777.1:n.1600-56_1600-36del
ENST00000647016.1:n.1747-56_1747-36del
ENST00000647152.1:c.538-56_538-36del ENSP00000495893.1:n.538-56_538-36del
ENST00000647209.1:c.*1136-56_*1136-36del ENSP00000495558.1:n.*1136-56_*1136-36del
ENST00000647346.1:n.2287-56_2287-36del
ENST00000299427.10:c.1267-56_1267-36del ENSP00000299427.6:n.1267-56_1267-36del
ENST00000524611.1:n.89_109del
ENST00000524924.1:n.222-56_222-36del
ENST00000532191.1:n.320-56_320-36del
ENST00000533371.5:c.538-56_538-36del ENSP00000437066.1:n.538-56_538-36del
ENST00000611494.4:c.1267-56_1267-36del ENSP00000484546.1:n.1267-56_1267-36del
NM_000391.3:c.1267-56_1267-36del NP_000382.3:n.1267-56_1267-36del
NM_000391.4:c.1267-56_1267-36del MANE Select NP_000382.3:n.1267-56_1267-36del