Canonical Allele Identifier: CA1950237258
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616740G= , CM000673.2:g.6616740G= GRCh38
NC_000011.9:g.6637971G= , CM000673.1:g.6637971G= GRCh37
NC_000011.8:g.6594547G= NCBI36
NG_008653.1:g.7722C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.693C= ENSP00000507321.1:p.Ala231=
ENST00000299427.12:c.807C= MANE Select ENSP00000299427.6:p.Ala269=
ENST00000436873.7:c.312+561C=
ENST00000524788.2:n.1966C=
ENST00000524903.2:n.2082C=
ENST00000528807.2:n.463C=
ENST00000530040.2:n.480-237C=
ENST00000533371.6:c.78C= ENSP00000437066.1:p.Ala26=
ENST00000642892.1:c.78C= ENSP00000494165.1:p.Ala26=
ENST00000643439.1:c.*547C= ENSP00000495849.1:n.*547C=
ENST00000643479.1:n.836C=
ENST00000643516.1:c.396-237C=
ENST00000644151.1:n.2246C=
ENST00000644218.1:c.807C= ENSP00000493574.1:p.Ala269=
ENST00000644683.1:c.*260C= ENSP00000494085.1:n.*260C=
ENST00000644810.1:c.528C= ENSP00000495895.1:p.Ala176=
ENST00000644831.1:n.983C=
ENST00000644933.1:c.78C= ENSP00000496133.1:p.Ala26=
ENST00000645020.1:n.2097C=
ENST00000645285.1:c.78C= ENSP00000495058.1:p.Ala26=
ENST00000645331.1:n.1173C=
ENST00000645620.1:c.78C= ENSP00000493657.1:p.Ala26=
ENST00000646777.1:n.983C=
ENST00000647016.1:n.1287C=
ENST00000647152.1:c.78C= ENSP00000495893.1:p.Ala26=
ENST00000647209.1:c.*676C= ENSP00000495558.1:n.*676C=
ENST00000647346.1:n.1827C=
ENST00000299427.10:c.807C= ENSP00000299427.6:p.Ala269=
ENST00000436873.6:c.451-237C= ENSP00000398136.2:n.451-237C=
ENST00000524788.1:n.507C=
ENST00000528807.1:n.357C=
ENST00000533371.5:c.78C= ENSP00000437066.1:p.Ala26=
ENST00000611494.4:c.807C= ENSP00000484546.1:p.Ala269=
NM_000391.3:c.807C= NP_000382.3:p.Ala269=
NM_000391.4:c.807C= MANE Select NP_000382.3:p.Ala269=