Canonical Allele Identifier: CA379476162
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617638C>G , CM000673.2:g.6617638C>G GRCh38
NC_000011.9:g.6638869C>G , CM000673.1:g.6638869C>G GRCh37
NC_000011.8:g.6595445C>G NCBI36
NG_008653.1:g.6824G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.254G>C ENSP00000507321.1:p.Trp85Ser
ENST00000299427.12:c.368G>C MANE Select ENSP00000299427.6:p.Trp123Ser
ENST00000428886.7:n.456G>C
ENST00000436873.7:c.172G>C
ENST00000524788.2:n.1380G>C
ENST00000524903.2:n.1496G>C
ENST00000528571.6:c.*108G>C ENSP00000434647.1:n.*108G>C
ENST00000530040.2:n.397G>C
ENST00000533371.6:c.-362G>C ENSP00000437066.1:n.-362G>C
ENST00000534644.6:n.369G>C
ENST00000642892.1:c.-309G>C ENSP00000494165.1:n.-309G>C
ENST00000643439.1:c.*108G>C ENSP00000495849.1:n.*108G>C
ENST00000643479.1:n.397G>C
ENST00000643516.1:c.255G>C
ENST00000644151.1:n.1660G>C
ENST00000644218.1:c.368G>C ENSP00000493574.1:p.Trp123Ser
ENST00000644683.1:c.368G>C ENSP00000494085.1:p.Trp123Ser
ENST00000644810.1:c.230-485G>C ENSP00000495895.1:n.230-485G>C
ENST00000644831.1:n.397G>C
ENST00000644933.1:c.-362G>C ENSP00000496133.1:n.-362G>C
ENST00000645020.1:n.1396G>C
ENST00000645285.1:c.-362G>C ENSP00000495058.1:n.-362G>C
ENST00000645331.1:n.390G>C
ENST00000645620.1:c.-304G>C ENSP00000493657.1:n.-304G>C
ENST00000646777.1:n.397G>C
ENST00000647016.1:n.701G>C
ENST00000647152.1:c.-362G>C ENSP00000495893.1:n.-362G>C
ENST00000647209.1:c.*237G>C ENSP00000495558.1:n.*237G>C
ENST00000647346.1:n.1388G>C
ENST00000299427.10:c.368G>C ENSP00000299427.6:p.Trp123Ser
ENST00000428886.6:n.390G>C
ENST00000436873.6:c.368G>C ENSP00000398136.2:p.Trp123Ser
ENST00000528571.5:c.*108G>C ENSP00000434647.1:n.*108G>C
ENST00000530040.1:n.480G>C
ENST00000533371.5:c.-362G>C ENSP00000437066.1:n.-362G>C
ENST00000534644.5:n.353G>C
ENST00000611494.4:c.368G>C ENSP00000484546.1:p.Trp123Ser
NM_000391.3:c.368G>C NP_000382.3:p.Trp123Ser
NM_000391.4:c.368G>C MANE Select NP_000382.3:p.Trp123Ser