Canonical Allele Identifier: CA1950236974
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616554_6616555delinsTG , CM000673.2:g.6616554_6616555delinsTG GRCh38
NC_000011.9:g.6637785_6637786delinsTG , CM000673.1:g.6637785_6637786delinsTG GRCh37
NC_000011.8:g.6594361_6594362delinsTG NCBI36
NG_008653.1:g.7907_7908delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.773-52_773-51delinsCA ENSP00000507321.1:n.773-52_773-51delinsCA
ENST00000299427.12:c.887-52_887-51delinsCA MANE Select ENSP00000299427.6:n.887-52_887-51delinsCA
ENST00000436873.7:c.313-481_313-480delinsCA
ENST00000524903.2:n.2267_2268delinsCA
ENST00000528807.2:n.648_649delinsCA
ENST00000530040.2:n.480-52_480-51delinsCA
ENST00000533371.6:c.158-52_158-51delinsCA ENSP00000437066.1:n.158-52_158-51delinsCA
ENST00000642892.1:c.158-52_158-51delinsCA ENSP00000494165.1:n.158-52_158-51delinsCA
ENST00000643439.1:c.*627-52_*627-51delinsCA ENSP00000495849.1:n.*627-52_*627-51delinsCA
ENST00000643479.1:n.1021_1022delinsCA
ENST00000643516.1:c.396-52_396-51delinsCA
ENST00000644218.1:c.886+106_886+107delinsCA ENSP00000493574.1:n.886+106_886+107delinsCA
ENST00000644683.1:c.*340-52_*340-51delinsCA ENSP00000494085.1:n.*340-52_*340-51delinsCA
ENST00000644810.1:c.608-52_608-51delinsCA ENSP00000495895.1:n.608-52_608-51delinsCA
ENST00000644831.1:n.1063-52_1063-51delinsCA
ENST00000644933.1:c.158-52_158-51delinsCA ENSP00000496133.1:n.158-52_158-51delinsCA
ENST00000645020.1:n.2282_2283delinsCA
ENST00000645285.1:c.157+106_157+107delinsCA ENSP00000495058.1:n.157+106_157+107delinsCA
ENST00000645331.1:n.1358_1359delinsCA
ENST00000645620.1:c.158-52_158-51delinsCA ENSP00000493657.1:n.158-52_158-51delinsCA
ENST00000646777.1:n.1168_1169delinsCA
ENST00000647016.1:n.1367-52_1367-51delinsCA
ENST00000647152.1:c.158-52_158-51delinsCA ENSP00000495893.1:n.158-52_158-51delinsCA
ENST00000647209.1:c.*756-52_*756-51delinsCA ENSP00000495558.1:n.*756-52_*756-51delinsCA
ENST00000647346.1:n.1907-52_1907-51delinsCA
ENST00000299427.10:c.887-52_887-51delinsCA ENSP00000299427.6:n.887-52_887-51delinsCA
ENST00000436873.6:c.451-52_451-51delinsCA ENSP00000398136.2:n.451-52_451-51delinsCA
ENST00000528807.1:n.542_543delinsCA
ENST00000533371.5:c.158-52_158-51delinsCA ENSP00000437066.1:n.158-52_158-51delinsCA
ENST00000611494.4:c.887-52_887-51delinsCA ENSP00000484546.1:n.887-52_887-51delinsCA
NM_000391.3:c.887-52_887-51delinsCA NP_000382.3:n.887-52_887-51delinsCA
NM_000391.4:c.887-52_887-51delinsCA MANE Select NP_000382.3:n.887-52_887-51delinsCA