Canonical Allele Identifier: CA597439882
Gene: TPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1203798488
gnomAD v2: 11-6636603-A-C
gnomAD v3: 11-6615372-A-C
gnomAD v4: 11-6615372-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6615372A>C , CM000673.2:g.6615372A>C GRCh38
NC_000011.9:g.6636603A>C , CM000673.1:g.6636603A>C GRCh37
NC_000011.8:g.6593179A>C NCBI36
NG_008653.1:g.9090T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.1153-43T>G ENSP00000507321.1:n.1153-43T>G
ENST00000299427.12:c.1267-43T>G MANE Select ENSP00000299427.6:n.1267-43T>G
ENST00000436873.7:c.504-43T>G
ENST00000524611.2:n.84T>G
ENST00000524924.2:n.387-43T>G
ENST00000533371.6:c.538-43T>G ENSP00000437066.1:n.538-43T>G
ENST00000642892.1:c.538-43T>G ENSP00000494165.1:n.538-43T>G
ENST00000643342.1:c.340-43T>G
ENST00000643439.1:c.*1007-43T>G ENSP00000495849.1:n.*1007-43T>G
ENST00000643479.1:n.1453-43T>G
ENST00000643516.1:c.776-43T>G
ENST00000644218.1:c.1078-43T>G ENSP00000493574.1:n.1078-43T>G
ENST00000644683.1:c.*720-43T>G ENSP00000494085.1:n.*720-43T>G
ENST00000644810.1:c.988-43T>G ENSP00000495895.1:n.988-43T>G
ENST00000644831.1:n.1443-43T>G
ENST00000644933.1:c.*133-43T>G ENSP00000496133.1:n.*133-43T>G
ENST00000645285.1:c.*133-43T>G ENSP00000495058.1:n.*133-43T>G
ENST00000645331.1:n.2472-43T>G
ENST00000645620.1:c.538-43T>G ENSP00000493657.1:n.538-43T>G
ENST00000646691.1:n.1111T>G
ENST00000646777.1:n.1600-43T>G
ENST00000647016.1:n.1747-43T>G
ENST00000647152.1:c.538-43T>G ENSP00000495893.1:n.538-43T>G
ENST00000647209.1:c.*1136-43T>G ENSP00000495558.1:n.*1136-43T>G
ENST00000647346.1:n.2287-43T>G
ENST00000299427.10:c.1267-43T>G ENSP00000299427.6:n.1267-43T>G
ENST00000524611.1:n.102T>G
ENST00000524924.1:n.222-43T>G
ENST00000532191.1:n.320-43T>G
ENST00000533371.5:c.538-43T>G ENSP00000437066.1:n.538-43T>G
ENST00000611494.4:c.1267-43T>G ENSP00000484546.1:n.1267-43T>G
NM_000391.3:c.1267-43T>G NP_000382.3:n.1267-43T>G
NM_000391.4:c.1267-43T>G MANE Select NP_000382.3:n.1267-43T>G