Canonical Allele Identifier: CA2790314278
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616504_6616505del , CM000673.2:g.6616504_6616505del GRCh38
NC_000011.9:g.6637735_6637736del , CM000673.1:g.6637735_6637736del GRCh37
NC_000011.8:g.6594311_6594312del NCBI36
NG_008653.1:g.7957_7958del

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.773-2_773-1del ENSP00000507321.1:n.773-2_773-1del
ENST00000299427.12:c.887-2_887-1del MANE Select ENSP00000299427.6:n.887-2_887-1del
ENST00000436873.7:c.313-431_313-430del
ENST00000530040.2:n.480-2_480-1del
ENST00000533371.6:c.158-2_158-1del ENSP00000437066.1:n.158-2_158-1del
ENST00000642892.1:c.158-2_158-1del ENSP00000494165.1:n.158-2_158-1del
ENST00000643439.1:c.*627-2_*627-1del ENSP00000495849.1:n.*627-2_*627-1del
ENST00000643479.1:n.1071_1072del
ENST00000643516.1:c.396-2_396-1del
ENST00000644218.1:c.886+156_886+157del ENSP00000493574.1:n.886+156_886+157del
ENST00000644683.1:c.*340-2_*340-1del ENSP00000494085.1:n.*340-2_*340-1del
ENST00000644810.1:c.608-2_608-1del ENSP00000495895.1:n.608-2_608-1del
ENST00000644831.1:n.1063-2_1063-1del
ENST00000644933.1:c.158-2_158-1del ENSP00000496133.1:n.158-2_158-1del
ENST00000645285.1:c.157+156_157+157del ENSP00000495058.1:n.157+156_157+157del
ENST00000645331.1:n.1408_1409del
ENST00000645620.1:c.158-2_158-1del ENSP00000493657.1:n.158-2_158-1del
ENST00000646777.1:n.1218_1219del
ENST00000647016.1:n.1367-2_1367-1del
ENST00000647152.1:c.158-2_158-1del ENSP00000495893.1:n.158-2_158-1del
ENST00000647209.1:c.*756-2_*756-1del ENSP00000495558.1:n.*756-2_*756-1del
ENST00000647346.1:n.1907-2_1907-1del
ENST00000299427.10:c.887-2_887-1del ENSP00000299427.6:n.887-2_887-1del
ENST00000436873.6:c.451-2_451-1del ENSP00000398136.2:n.451-2_451-1del
ENST00000533371.5:c.158-2_158-1del ENSP00000437066.1:n.158-2_158-1del
ENST00000611494.4:c.887-2_887-1del ENSP00000484546.1:n.887-2_887-1del
NM_000391.3:c.887-2_887-1del NP_000382.3:n.887-2_887-1del
NM_000391.4:c.887-2_887-1del MANE Select NP_000382.3:n.887-2_887-1del