Canonical Allele Identifier: CA379476121
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617626C>G , CM000673.2:g.6617626C>G GRCh38
NC_000011.9:g.6638857C>G , CM000673.1:g.6638857C>G GRCh37
NC_000011.8:g.6595433C>G NCBI36
NG_008653.1:g.6836G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.266G>C ENSP00000507321.1:p.Arg89Pro
ENST00000299427.12:c.380G>C MANE Select ENSP00000299427.6:p.Arg127Pro
ENST00000428886.7:n.468G>C
ENST00000436873.7:c.184G>C
ENST00000524788.2:n.1392G>C
ENST00000524903.2:n.1508G>C
ENST00000528571.6:c.*120G>C ENSP00000434647.1:n.*120G>C
ENST00000530040.2:n.409G>C
ENST00000533371.6:c.-350G>C ENSP00000437066.1:n.-350G>C
ENST00000534644.6:n.381G>C
ENST00000642892.1:c.-297G>C ENSP00000494165.1:n.-297G>C
ENST00000643439.1:c.*120G>C ENSP00000495849.1:n.*120G>C
ENST00000643479.1:n.409G>C
ENST00000643516.1:c.267G>C
ENST00000644151.1:n.1672G>C
ENST00000644218.1:c.380G>C ENSP00000493574.1:p.Arg127Pro
ENST00000644683.1:c.380G>C ENSP00000494085.1:p.Arg127Pro
ENST00000644810.1:c.230-473G>C ENSP00000495895.1:n.230-473G>C
ENST00000644831.1:n.409G>C
ENST00000644933.1:c.-350G>C ENSP00000496133.1:n.-350G>C
ENST00000645020.1:n.1408G>C
ENST00000645285.1:c.-350G>C ENSP00000495058.1:n.-350G>C
ENST00000645331.1:n.402G>C
ENST00000645620.1:c.-292G>C ENSP00000493657.1:n.-292G>C
ENST00000646777.1:n.409G>C
ENST00000647016.1:n.713G>C
ENST00000647152.1:c.-350G>C ENSP00000495893.1:n.-350G>C
ENST00000647209.1:c.*249G>C ENSP00000495558.1:n.*249G>C
ENST00000647346.1:n.1400G>C
ENST00000299427.10:c.380G>C ENSP00000299427.6:p.Arg127Pro
ENST00000428886.6:n.402G>C
ENST00000436873.6:c.380G>C ENSP00000398136.2:p.Arg127Pro
ENST00000528571.5:c.*120G>C ENSP00000434647.1:n.*120G>C
ENST00000530040.1:n.492G>C
ENST00000533371.5:c.-350G>C ENSP00000437066.1:n.-350G>C
ENST00000534644.5:n.365G>C
ENST00000611494.4:c.380G>C ENSP00000484546.1:p.Arg127Pro
NM_000391.3:c.380G>C NP_000382.3:p.Arg127Pro
NM_000391.4:c.380G>C MANE Select NP_000382.3:p.Arg127Pro