Canonical Allele Identifier: CA1950215359
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617732A= , CM000673.2:g.6617732A= GRCh38
NC_000011.9:g.6638963A= , CM000673.1:g.6638963A= GRCh37
NC_000011.8:g.6595539A= NCBI36
NG_008653.1:g.6730T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.160T= ENSP00000507321.1:p.Ser54=
ENST00000299427.12:c.274T= MANE Select ENSP00000299427.6:p.Ser92=
ENST00000428886.7:n.362T=
ENST00000436873.7:c.78T=
ENST00000524788.2:n.1286T=
ENST00000524903.2:n.1402T=
ENST00000528571.6:c.*14T= ENSP00000434647.1:n.*14T=
ENST00000530040.2:n.303T=
ENST00000533371.6:c.-456T= ENSP00000437066.1:n.-456T=
ENST00000534644.6:n.275T=
ENST00000642892.1:c.-403T= ENSP00000494165.1:n.-403T=
ENST00000643439.1:c.*14T= ENSP00000495849.1:n.*14T=
ENST00000643479.1:n.303T=
ENST00000643516.1:c.161T=
ENST00000644151.1:n.1566T=
ENST00000644218.1:c.274T= ENSP00000493574.1:p.Ser92=
ENST00000644683.1:c.274T= ENSP00000494085.1:p.Ser92=
ENST00000644810.1:c.230-579T= ENSP00000495895.1:n.230-579T=
ENST00000644831.1:n.303T=
ENST00000644933.1:c.-456T= ENSP00000496133.1:n.-456T=
ENST00000645020.1:n.1302T=
ENST00000645285.1:c.-456T= ENSP00000495058.1:n.-456T=
ENST00000645331.1:n.296T=
ENST00000645620.1:c.-398T= ENSP00000493657.1:n.-398T=
ENST00000646777.1:n.303T=
ENST00000647016.1:n.607T=
ENST00000647152.1:c.-456T= ENSP00000495893.1:n.-456T=
ENST00000647209.1:c.*143T= ENSP00000495558.1:n.*143T=
ENST00000647346.1:n.1294T=
ENST00000299427.10:c.274T= ENSP00000299427.6:p.Ser92=
ENST00000428886.6:n.296T=
ENST00000436873.6:c.274T= ENSP00000398136.2:p.Ser92=
ENST00000528571.5:c.*14T= ENSP00000434647.1:n.*14T=
ENST00000530040.1:n.386T=
ENST00000533371.5:c.-456T= ENSP00000437066.1:n.-456T=
ENST00000534644.5:n.259T=
ENST00000611494.4:c.274T= ENSP00000484546.1:p.Ser92=
NM_000391.3:c.274T= NP_000382.3:p.Ser92=
NM_000391.4:c.274T= MANE Select NP_000382.3:p.Ser92=