Canonical Allele Identifier: CA2790314311
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616562_6616564del , CM000673.2:g.6616562_6616564del GRCh38
NC_000011.9:g.6637793_6637795del , CM000673.1:g.6637793_6637795del GRCh37
NC_000011.8:g.6594369_6594371del NCBI36
NG_008653.1:g.7898_7900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.773-61_773-59del ENSP00000507321.1:n.773-61_773-59del
ENST00000299427.12:c.887-61_887-59del MANE Select ENSP00000299427.6:n.887-61_887-59del
ENST00000436873.7:c.313-490_313-488del
ENST00000524903.2:n.2258_2260del
ENST00000528807.2:n.639_641del
ENST00000530040.2:n.480-61_480-59del
ENST00000533371.6:c.158-61_158-59del ENSP00000437066.1:n.158-61_158-59del
ENST00000642892.1:c.158-61_158-59del ENSP00000494165.1:n.158-61_158-59del
ENST00000643439.1:c.*627-61_*627-59del ENSP00000495849.1:n.*627-61_*627-59del
ENST00000643479.1:n.1012_1014del
ENST00000643516.1:c.396-61_396-59del
ENST00000644218.1:c.886+97_886+99del ENSP00000493574.1:n.886+97_886+99del
ENST00000644683.1:c.*340-61_*340-59del ENSP00000494085.1:n.*340-61_*340-59del
ENST00000644810.1:c.608-61_608-59del ENSP00000495895.1:n.608-61_608-59del
ENST00000644831.1:n.1063-61_1063-59del
ENST00000644933.1:c.158-61_158-59del ENSP00000496133.1:n.158-61_158-59del
ENST00000645020.1:n.2273_2275del
ENST00000645285.1:c.157+97_157+99del ENSP00000495058.1:n.157+97_157+99del
ENST00000645331.1:n.1349_1351del
ENST00000645620.1:c.158-61_158-59del ENSP00000493657.1:n.158-61_158-59del
ENST00000646777.1:n.1159_1161del
ENST00000647016.1:n.1367-61_1367-59del
ENST00000647152.1:c.158-61_158-59del ENSP00000495893.1:n.158-61_158-59del
ENST00000647209.1:c.*756-61_*756-59del ENSP00000495558.1:n.*756-61_*756-59del
ENST00000647346.1:n.1907-61_1907-59del
ENST00000299427.10:c.887-61_887-59del ENSP00000299427.6:n.887-61_887-59del
ENST00000436873.6:c.451-61_451-59del ENSP00000398136.2:n.451-61_451-59del
ENST00000528807.1:n.533_535del
ENST00000533371.5:c.158-61_158-59del ENSP00000437066.1:n.158-61_158-59del
ENST00000611494.4:c.887-61_887-59del ENSP00000484546.1:n.887-61_887-59del
NM_000391.3:c.887-61_887-59del NP_000382.3:n.887-61_887-59del
NM_000391.4:c.887-61_887-59del MANE Select NP_000382.3:n.887-61_887-59del