Canonical Allele Identifier: CA1950215356
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617731G= , CM000673.2:g.6617731G= GRCh38
NC_000011.9:g.6638962G= , CM000673.1:g.6638962G= GRCh37
NC_000011.8:g.6595538G= NCBI36
NG_008653.1:g.6731C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.161C= ENSP00000507321.1:p.Ser54=
ENST00000299427.12:c.275C= MANE Select ENSP00000299427.6:p.Ser92=
ENST00000428886.7:n.363C=
ENST00000436873.7:c.79C=
ENST00000524788.2:n.1287C=
ENST00000524903.2:n.1403C=
ENST00000528571.6:c.*15C= ENSP00000434647.1:n.*15C=
ENST00000530040.2:n.304C=
ENST00000533371.6:c.-455C= ENSP00000437066.1:n.-455C=
ENST00000534644.6:n.276C=
ENST00000642892.1:c.-402C= ENSP00000494165.1:n.-402C=
ENST00000643439.1:c.*15C= ENSP00000495849.1:n.*15C=
ENST00000643479.1:n.304C=
ENST00000643516.1:c.162C=
ENST00000644151.1:n.1567C=
ENST00000644218.1:c.275C= ENSP00000493574.1:p.Ser92=
ENST00000644683.1:c.275C= ENSP00000494085.1:p.Ser92=
ENST00000644810.1:c.230-578C= ENSP00000495895.1:n.230-578C=
ENST00000644831.1:n.304C=
ENST00000644933.1:c.-455C= ENSP00000496133.1:n.-455C=
ENST00000645020.1:n.1303C=
ENST00000645285.1:c.-455C= ENSP00000495058.1:n.-455C=
ENST00000645331.1:n.297C=
ENST00000645620.1:c.-397C= ENSP00000493657.1:n.-397C=
ENST00000646777.1:n.304C=
ENST00000647016.1:n.608C=
ENST00000647152.1:c.-455C= ENSP00000495893.1:n.-455C=
ENST00000647209.1:c.*144C= ENSP00000495558.1:n.*144C=
ENST00000647346.1:n.1295C=
ENST00000299427.10:c.275C= ENSP00000299427.6:p.Ser92=
ENST00000428886.6:n.297C=
ENST00000436873.6:c.275C= ENSP00000398136.2:p.Ser92=
ENST00000528571.5:c.*15C= ENSP00000434647.1:n.*15C=
ENST00000530040.1:n.387C=
ENST00000533371.5:c.-455C= ENSP00000437066.1:n.-455C=
ENST00000534644.5:n.260C=
ENST00000611494.4:c.275C= ENSP00000484546.1:p.Ser92=
NM_000391.3:c.275C= NP_000382.3:p.Ser92=
NM_000391.4:c.275C= MANE Select NP_000382.3:p.Ser92=