Canonical Allele Identifier: CA1950237219
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616721C= , CM000673.2:g.6616721C= GRCh38
NC_000011.9:g.6637952C= , CM000673.1:g.6637952C= GRCh37
NC_000011.8:g.6594528C= NCBI36
NG_008653.1:g.7741G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.712G= ENSP00000507321.1:p.Asp238=
ENST00000299427.12:c.826G= MANE Select ENSP00000299427.6:p.Asp276=
ENST00000436873.7:c.312+580G=
ENST00000524788.2:n.1985G=
ENST00000524903.2:n.2101G=
ENST00000528807.2:n.482G=
ENST00000530040.2:n.480-218G=
ENST00000533371.6:c.97G= ENSP00000437066.1:p.Asp33=
ENST00000642892.1:c.97G= ENSP00000494165.1:p.Asp33=
ENST00000643439.1:c.*566G= ENSP00000495849.1:n.*566G=
ENST00000643479.1:n.855G=
ENST00000643516.1:c.396-218G=
ENST00000644151.1:n.2265G=
ENST00000644218.1:c.826G= ENSP00000493574.1:p.Asp276=
ENST00000644683.1:c.*279G= ENSP00000494085.1:n.*279G=
ENST00000644810.1:c.547G= ENSP00000495895.1:p.Asp183=
ENST00000644831.1:n.1002G=
ENST00000644933.1:c.97G= ENSP00000496133.1:p.Asp33=
ENST00000645020.1:n.2116G=
ENST00000645285.1:c.97G= ENSP00000495058.1:p.Asp33=
ENST00000645331.1:n.1192G=
ENST00000645620.1:c.97G= ENSP00000493657.1:p.Asp33=
ENST00000646777.1:n.1002G=
ENST00000647016.1:n.1306G=
ENST00000647152.1:c.97G= ENSP00000495893.1:p.Asp33=
ENST00000647209.1:c.*695G= ENSP00000495558.1:n.*695G=
ENST00000647346.1:n.1846G=
ENST00000299427.10:c.826G= ENSP00000299427.6:p.Asp276=
ENST00000436873.6:c.451-218G= ENSP00000398136.2:n.451-218G=
ENST00000524788.1:n.526G=
ENST00000528807.1:n.376G=
ENST00000533371.5:c.97G= ENSP00000437066.1:p.Asp33=
ENST00000611494.4:c.826G= ENSP00000484546.1:p.Asp276=
NM_000391.3:c.826G= NP_000382.3:p.Asp276=
NM_000391.4:c.826G= MANE Select NP_000382.3:p.Asp276=