Canonical Allele Identifier: CA5858689
Gene: TPP1 HGNC NCBI

Linked Data

dbSNP Id: rs764434423
gnomAD v2: 11-6636610-A-T
gnomAD v4: 11-6615379-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6615379A>T , CM000673.2:g.6615379A>T GRCh38
NC_000011.9:g.6636610A>T , CM000673.1:g.6636610A>T GRCh37
NC_000011.8:g.6593186A>T NCBI36
NG_008653.1:g.9083T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.1153-50T>A ENSP00000507321.1:n.1153-50T>A
ENST00000299427.12:c.1267-50T>A MANE Select ENSP00000299427.6:n.1267-50T>A
ENST00000436873.7:c.504-50T>A
ENST00000524611.2:n.77T>A
ENST00000524924.2:n.387-50T>A
ENST00000533371.6:c.538-50T>A ENSP00000437066.1:n.538-50T>A
ENST00000642892.1:c.538-50T>A ENSP00000494165.1:n.538-50T>A
ENST00000643342.1:c.340-50T>A
ENST00000643439.1:c.*1007-50T>A ENSP00000495849.1:n.*1007-50T>A
ENST00000643479.1:n.1453-50T>A
ENST00000643516.1:c.776-50T>A
ENST00000644218.1:c.1078-50T>A ENSP00000493574.1:n.1078-50T>A
ENST00000644683.1:c.*720-50T>A ENSP00000494085.1:n.*720-50T>A
ENST00000644810.1:c.988-50T>A ENSP00000495895.1:n.988-50T>A
ENST00000644831.1:n.1443-50T>A
ENST00000644933.1:c.*133-50T>A ENSP00000496133.1:n.*133-50T>A
ENST00000645285.1:c.*133-50T>A ENSP00000495058.1:n.*133-50T>A
ENST00000645331.1:n.2472-50T>A
ENST00000645620.1:c.538-50T>A ENSP00000493657.1:n.538-50T>A
ENST00000646691.1:n.1104T>A
ENST00000646777.1:n.1600-50T>A
ENST00000647016.1:n.1747-50T>A
ENST00000647152.1:c.538-50T>A ENSP00000495893.1:n.538-50T>A
ENST00000647209.1:c.*1136-50T>A ENSP00000495558.1:n.*1136-50T>A
ENST00000647346.1:n.2287-50T>A
ENST00000299427.10:c.1267-50T>A ENSP00000299427.6:n.1267-50T>A
ENST00000524611.1:n.95T>A
ENST00000524924.1:n.222-50T>A
ENST00000532191.1:n.320-50T>A
ENST00000533371.5:c.538-50T>A ENSP00000437066.1:n.538-50T>A
ENST00000611494.4:c.1267-50T>A ENSP00000484546.1:n.1267-50T>A
NM_000391.3:c.1267-50T>A NP_000382.3:n.1267-50T>A
NM_000391.4:c.1267-50T>A MANE Select NP_000382.3:n.1267-50T>A