Canonical Allele Identifier: CA1950215363
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617735G= , CM000673.2:g.6617735G= GRCh38
NC_000011.9:g.6638966G= , CM000673.1:g.6638966G= GRCh37
NC_000011.8:g.6595542G= NCBI36
NG_008653.1:g.6727C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.157C= ENSP00000507321.1:p.Pro53=
ENST00000299427.12:c.271C= MANE Select ENSP00000299427.6:p.Pro91=
ENST00000428886.7:n.359C=
ENST00000436873.7:c.75C=
ENST00000524788.2:n.1283C=
ENST00000524903.2:n.1399C=
ENST00000528571.6:c.*11C= ENSP00000434647.1:n.*11C=
ENST00000530040.2:n.300C=
ENST00000533371.6:c.-459C= ENSP00000437066.1:n.-459C=
ENST00000534644.6:n.272C=
ENST00000642892.1:c.-406C= ENSP00000494165.1:n.-406C=
ENST00000643439.1:c.*11C= ENSP00000495849.1:n.*11C=
ENST00000643479.1:n.300C=
ENST00000643516.1:c.158C=
ENST00000644151.1:n.1563C=
ENST00000644218.1:c.271C= ENSP00000493574.1:p.Pro91=
ENST00000644683.1:c.271C= ENSP00000494085.1:p.Pro91=
ENST00000644810.1:c.230-582C= ENSP00000495895.1:n.230-582C=
ENST00000644831.1:n.300C=
ENST00000644933.1:c.-459C= ENSP00000496133.1:n.-459C=
ENST00000645020.1:n.1299C=
ENST00000645285.1:c.-459C= ENSP00000495058.1:n.-459C=
ENST00000645331.1:n.293C=
ENST00000645620.1:c.-401C= ENSP00000493657.1:n.-401C=
ENST00000646777.1:n.300C=
ENST00000647016.1:n.604C=
ENST00000647152.1:c.-459C= ENSP00000495893.1:n.-459C=
ENST00000647209.1:c.*140C= ENSP00000495558.1:n.*140C=
ENST00000647346.1:n.1291C=
ENST00000299427.10:c.271C= ENSP00000299427.6:p.Pro91=
ENST00000428886.6:n.293C=
ENST00000436873.6:c.271C= ENSP00000398136.2:p.Pro91=
ENST00000528571.5:c.*11C= ENSP00000434647.1:n.*11C=
ENST00000530040.1:n.383C=
ENST00000533371.5:c.-459C= ENSP00000437066.1:n.-459C=
ENST00000534644.5:n.256C=
ENST00000611494.4:c.271C= ENSP00000484546.1:p.Pro91=
NM_000391.3:c.271C= NP_000382.3:p.Pro91=
NM_000391.4:c.271C= MANE Select NP_000382.3:p.Pro91=