Canonical Allele Identifier: CA1950214973
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617420T= , CM000673.2:g.6617420T= GRCh38
NC_000011.9:g.6638651T= , CM000673.1:g.6638651T= GRCh37
NC_000011.8:g.6595227T= NCBI36
NG_008653.1:g.7042A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.275A= ENSP00000507321.1:p.Glu92=
ENST00000299427.12:c.389A= MANE Select ENSP00000299427.6:p.Glu130=
ENST00000428886.7:n.477A=
ENST00000436873.7:c.193A=
ENST00000524788.2:n.1401A=
ENST00000524903.2:n.1517A=
ENST00000528571.6:c.*129A= ENSP00000434647.1:n.*129A=
ENST00000528807.2:n.45A=
ENST00000530040.2:n.418A=
ENST00000533371.6:c.-341A= ENSP00000437066.1:n.-341A=
ENST00000534644.6:n.390A=
ENST00000642892.1:c.-288A= ENSP00000494165.1:n.-288A=
ENST00000643439.1:c.*129A= ENSP00000495849.1:n.*129A=
ENST00000643479.1:n.418A=
ENST00000643516.1:c.276A=
ENST00000644151.1:n.1681A=
ENST00000644218.1:c.389A= ENSP00000493574.1:p.Glu130=
ENST00000644683.1:c.389A= ENSP00000494085.1:p.Glu130=
ENST00000644810.1:c.230-267A= ENSP00000495895.1:n.230-267A=
ENST00000644831.1:n.418A=
ENST00000644933.1:c.-341A= ENSP00000496133.1:n.-341A=
ENST00000645020.1:n.1417A=
ENST00000645285.1:c.-341A= ENSP00000495058.1:n.-341A=
ENST00000645331.1:n.608A=
ENST00000645620.1:c.-283A= ENSP00000493657.1:n.-283A=
ENST00000646777.1:n.418A=
ENST00000647016.1:n.722A=
ENST00000647152.1:c.-341A= ENSP00000495893.1:n.-341A=
ENST00000647209.1:c.*258A= ENSP00000495558.1:n.*258A=
ENST00000647346.1:n.1409A=
ENST00000299427.10:c.389A= ENSP00000299427.6:p.Glu130=
ENST00000428886.6:n.411A=
ENST00000436873.6:c.389A= ENSP00000398136.2:p.Glu130=
ENST00000528571.5:c.*129A= ENSP00000434647.1:n.*129A=
ENST00000530040.1:n.501A=
ENST00000533371.5:c.-341A= ENSP00000437066.1:n.-341A=
ENST00000534644.5:n.374A=
ENST00000611494.4:c.389A= ENSP00000484546.1:p.Glu130=
NM_000391.3:c.389A= NP_000382.3:p.Glu130=
NM_000391.4:c.389A= MANE Select NP_000382.3:p.Glu130=