Canonical Allele Identifier: CA2739276122
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2838151
ClinVar RCV Id: RCV003694897

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617782G>A , CM000673.2:g.6617782G>A GRCh38
NC_000011.9:g.6639013G>A , CM000673.1:g.6639013G>A GRCh37
NC_000011.8:g.6595589G>A NCBI36
NG_008653.1:g.6680C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.116-6C>T ENSP00000507321.1:n.116-6C>T
ENST00000299427.12:c.230-6C>T MANE Select ENSP00000299427.6:n.230-6C>T
ENST00000428886.7:n.318-6C>T
ENST00000436873.7:c.34-6C>T
ENST00000524788.2:n.1236C>T
ENST00000524903.2:n.1352C>T
ENST00000528571.6:c.90-6C>T ENSP00000434647.1:n.90-6C>T
ENST00000530040.2:n.259-6C>T
ENST00000533371.6:c.-500-6C>T ENSP00000437066.1:n.-500-6C>T
ENST00000534644.6:n.231-6C>T
ENST00000642892.1:c.-447-6C>T ENSP00000494165.1:n.-447-6C>T
ENST00000643439.1:c.90-6C>T ENSP00000495849.1:n.90-6C>T
ENST00000643479.1:n.259-6C>T
ENST00000643516.1:c.117-6C>T
ENST00000644151.1:n.1516C>T
ENST00000644218.1:c.230-6C>T ENSP00000493574.1:n.230-6C>T
ENST00000644683.1:c.230-6C>T ENSP00000494085.1:n.230-6C>T
ENST00000644810.1:c.230-629C>T ENSP00000495895.1:n.230-629C>T
ENST00000644831.1:n.259-6C>T
ENST00000644933.1:c.-500-6C>T ENSP00000496133.1:n.-500-6C>T
ENST00000645020.1:n.1252C>T
ENST00000645285.1:c.-500-6C>T ENSP00000495058.1:n.-500-6C>T
ENST00000645331.1:n.252-6C>T
ENST00000645620.1:c.-442-6C>T ENSP00000493657.1:n.-442-6C>T
ENST00000646777.1:n.259-6C>T
ENST00000647016.1:n.557C>T
ENST00000647152.1:c.-500-6C>T ENSP00000495893.1:n.-500-6C>T
ENST00000647209.1:c.*99-6C>T ENSP00000495558.1:n.*99-6C>T
ENST00000647346.1:n.1244C>T
ENST00000299427.10:c.230-6C>T ENSP00000299427.6:n.230-6C>T
ENST00000428886.6:n.252-6C>T
ENST00000436873.6:c.230-6C>T ENSP00000398136.2:n.230-6C>T
ENST00000528571.5:c.90-6C>T ENSP00000434647.1:n.90-6C>T
ENST00000528917.1:n.531-6C>T
ENST00000530040.1:n.342-6C>T
ENST00000533371.5:c.-500-6C>T ENSP00000437066.1:n.-500-6C>T
ENST00000534644.5:n.215-6C>T
ENST00000611494.4:c.230-6C>T ENSP00000484546.1:n.230-6C>T
NM_000391.3:c.230-6C>T NP_000382.3:n.230-6C>T
NM_000391.4:c.230-6C>T MANE Select NP_000382.3:n.230-6C>T