Canonical Allele Identifier: CA2790314281
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616506_6616507del , CM000673.2:g.6616506_6616507del GRCh38
NC_000011.9:g.6637737_6637738del , CM000673.1:g.6637737_6637738del GRCh37
NC_000011.8:g.6594313_6594314del NCBI36
NG_008653.1:g.7955_7956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.773-4_773-3del ENSP00000507321.1:n.773-4_773-3del
ENST00000299427.12:c.887-4_887-3del MANE Select ENSP00000299427.6:n.887-4_887-3del
ENST00000436873.7:c.313-433_313-432del
ENST00000530040.2:n.480-4_480-3del
ENST00000533371.6:c.158-4_158-3del ENSP00000437066.1:n.158-4_158-3del
ENST00000642892.1:c.158-4_158-3del ENSP00000494165.1:n.158-4_158-3del
ENST00000643439.1:c.*627-4_*627-3del ENSP00000495849.1:n.*627-4_*627-3del
ENST00000643479.1:n.1069_1070del
ENST00000643516.1:c.396-4_396-3del
ENST00000644218.1:c.886+154_886+155del ENSP00000493574.1:n.886+154_886+155del
ENST00000644683.1:c.*340-4_*340-3del ENSP00000494085.1:n.*340-4_*340-3del
ENST00000644810.1:c.608-4_608-3del ENSP00000495895.1:n.608-4_608-3del
ENST00000644831.1:n.1063-4_1063-3del
ENST00000644933.1:c.158-4_158-3del ENSP00000496133.1:n.158-4_158-3del
ENST00000645285.1:c.157+154_157+155del ENSP00000495058.1:n.157+154_157+155del
ENST00000645331.1:n.1406_1407del
ENST00000645620.1:c.158-4_158-3del ENSP00000493657.1:n.158-4_158-3del
ENST00000646777.1:n.1216_1217del
ENST00000647016.1:n.1367-4_1367-3del
ENST00000647152.1:c.158-4_158-3del ENSP00000495893.1:n.158-4_158-3del
ENST00000647209.1:c.*756-4_*756-3del ENSP00000495558.1:n.*756-4_*756-3del
ENST00000647346.1:n.1907-4_1907-3del
ENST00000299427.10:c.887-4_887-3del ENSP00000299427.6:n.887-4_887-3del
ENST00000436873.6:c.451-4_451-3del ENSP00000398136.2:n.451-4_451-3del
ENST00000533371.5:c.158-4_158-3del ENSP00000437066.1:n.158-4_158-3del
ENST00000611494.4:c.887-4_887-3del ENSP00000484546.1:n.887-4_887-3del
NM_000391.3:c.887-4_887-3del NP_000382.3:n.887-4_887-3del
NM_000391.4:c.887-4_887-3del MANE Select NP_000382.3:n.887-4_887-3del