Canonical Allele Identifier: CA1950237351
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616786T= , CM000673.2:g.6616786T= GRCh38
NC_000011.9:g.6638017T= , CM000673.1:g.6638017T= GRCh37
NC_000011.8:g.6594593T= NCBI36
NG_008653.1:g.7676A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.647A= ENSP00000507321.1:p.Gln216=
ENST00000299427.12:c.761A= MANE Select ENSP00000299427.6:p.Gln254=
ENST00000436873.7:c.312+515A=
ENST00000524788.2:n.1920A=
ENST00000524903.2:n.2036A=
ENST00000528807.2:n.417A=
ENST00000530040.2:n.480-283A=
ENST00000533371.6:c.32A= ENSP00000437066.1:p.Gln11=
ENST00000642892.1:c.32A= ENSP00000494165.1:p.Gln11=
ENST00000643439.1:c.*501A= ENSP00000495849.1:n.*501A=
ENST00000643479.1:n.790A=
ENST00000643516.1:c.396-283A=
ENST00000644151.1:n.2200A=
ENST00000644218.1:c.761A= ENSP00000493574.1:p.Gln254=
ENST00000644683.1:c.*214A= ENSP00000494085.1:n.*214A=
ENST00000644810.1:c.482A= ENSP00000495895.1:p.Gln161=
ENST00000644831.1:n.937A=
ENST00000644933.1:c.32A= ENSP00000496133.1:p.Gln11=
ENST00000645020.1:n.2051A=
ENST00000645285.1:c.32A= ENSP00000495058.1:p.Gln11=
ENST00000645331.1:n.1127A=
ENST00000645620.1:c.32A= ENSP00000493657.1:p.Gln11=
ENST00000646777.1:n.937A=
ENST00000647016.1:n.1241A=
ENST00000647152.1:c.32A= ENSP00000495893.1:p.Gln11=
ENST00000647209.1:c.*630A= ENSP00000495558.1:n.*630A=
ENST00000647346.1:n.1781A=
ENST00000299427.10:c.761A= ENSP00000299427.6:p.Gln254=
ENST00000436873.6:c.451-283A= ENSP00000398136.2:n.451-283A=
ENST00000524788.1:n.461A=
ENST00000528807.1:n.311A=
ENST00000533371.5:c.32A= ENSP00000437066.1:p.Gln11=
ENST00000611494.4:c.761A= ENSP00000484546.1:p.Gln254=
NM_000391.3:c.761A= NP_000382.3:p.Gln254=
NM_000391.4:c.761A= MANE Select NP_000382.3:p.Gln254=