Canonical Allele Identifier: CA1950237947
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617077G= , CM000673.2:g.6617077G= GRCh38
NC_000011.9:g.6638308G= , CM000673.1:g.6638308G= GRCh37
NC_000011.8:g.6594884G= NCBI36
NG_008653.1:g.7385C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.471C= ENSP00000507321.1:p.Gly157=
ENST00000299427.12:c.585C= MANE Select ENSP00000299427.6:p.Gly195=
ENST00000428886.7:n.820C=
ENST00000436873.7:c.312+224C=
ENST00000524788.2:n.1744C=
ENST00000524903.2:n.1860C=
ENST00000528807.2:n.241C=
ENST00000530040.2:n.479+282C=
ENST00000533371.6:c.-145C= ENSP00000437066.1:n.-145C=
ENST00000534644.6:n.533C=
ENST00000642892.1:c.-145C= ENSP00000494165.1:n.-145C=
ENST00000643439.1:c.*325C= ENSP00000495849.1:n.*325C=
ENST00000643479.1:n.614C=
ENST00000643516.1:c.395+224C=
ENST00000644151.1:n.2024C=
ENST00000644218.1:c.585C= ENSP00000493574.1:p.Gly195=
ENST00000644683.1:c.*38C= ENSP00000494085.1:n.*38C=
ENST00000644810.1:c.306C= ENSP00000495895.1:p.Gly102=
ENST00000644831.1:n.761C=
ENST00000644933.1:c.-145C= ENSP00000496133.1:n.-145C=
ENST00000645020.1:n.1760C=
ENST00000645285.1:c.-145C= ENSP00000495058.1:n.-145C=
ENST00000645331.1:n.951C=
ENST00000645620.1:c.-145C= ENSP00000493657.1:n.-145C=
ENST00000646777.1:n.761C=
ENST00000647016.1:n.1065C=
ENST00000647152.1:c.-145C= ENSP00000495893.1:n.-145C=
ENST00000647209.1:c.*454C= ENSP00000495558.1:n.*454C=
ENST00000647346.1:n.1605C=
ENST00000299427.10:c.585C= ENSP00000299427.6:p.Gly195=
ENST00000428886.6:n.754C=
ENST00000436873.6:c.450+282C= ENSP00000398136.2:n.450+282C=
ENST00000524788.1:n.285C=
ENST00000528571.5:c.*325C= ENSP00000434647.1:n.*325C=
ENST00000528807.1:n.135C=
ENST00000533371.5:c.-145C= ENSP00000437066.1:n.-145C=
ENST00000534644.5:n.570C=
ENST00000611494.4:c.585C= ENSP00000484546.1:p.Gly195=
NM_000391.3:c.585C= NP_000382.3:p.Gly195=
NM_000391.4:c.585C= MANE Select NP_000382.3:p.Gly195=