Canonical Allele Identifier: CA1950238249
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617177G= , CM000673.2:g.6617177G= GRCh38
NC_000011.9:g.6638408G= , CM000673.1:g.6638408G= GRCh37
NC_000011.8:g.6594984G= NCBI36
NG_008653.1:g.7285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.395-24C= ENSP00000507321.1:n.395-24C=
ENST00000299427.12:c.509-24C= MANE Select ENSP00000299427.6:n.509-24C=
ENST00000428886.7:n.720C=
ENST00000436873.7:c.312+124C=
ENST00000524788.2:n.1644C=
ENST00000524903.2:n.1760C=
ENST00000528807.2:n.165-24C=
ENST00000530040.2:n.479+182C=
ENST00000533371.6:c.-221-24C= ENSP00000437066.1:n.-221-24C=
ENST00000534644.6:n.457-24C=
ENST00000642892.1:c.-221-24C= ENSP00000494165.1:n.-221-24C=
ENST00000643439.1:c.*249-24C= ENSP00000495849.1:n.*249-24C=
ENST00000643479.1:n.538-24C=
ENST00000643516.1:c.395+124C=
ENST00000644151.1:n.1924C=
ENST00000644218.1:c.509-24C= ENSP00000493574.1:n.509-24C=
ENST00000644683.1:c.451-24C= ENSP00000494085.1:n.451-24C=
ENST00000644810.1:c.230-24C= ENSP00000495895.1:n.230-24C=
ENST00000644831.1:n.661C=
ENST00000644933.1:c.-221-24C= ENSP00000496133.1:n.-221-24C=
ENST00000645020.1:n.1660C=
ENST00000645285.1:c.-221-24C= ENSP00000495058.1:n.-221-24C=
ENST00000645331.1:n.851C=
ENST00000645620.1:c.-221-24C= ENSP00000493657.1:n.-221-24C=
ENST00000646777.1:n.661C=
ENST00000647016.1:n.965C=
ENST00000647152.1:c.-221-24C= ENSP00000495893.1:n.-221-24C=
ENST00000647209.1:c.*378-24C= ENSP00000495558.1:n.*378-24C=
ENST00000647346.1:n.1529-24C=
ENST00000299427.10:c.509-24C= ENSP00000299427.6:n.509-24C=
ENST00000428886.6:n.654C=
ENST00000436873.6:c.450+182C= ENSP00000398136.2:n.450+182C=
ENST00000524788.1:n.185C=
ENST00000528571.5:c.*249-24C= ENSP00000434647.1:n.*249-24C=
ENST00000528807.1:n.35C=
ENST00000533371.5:c.-221-24C= ENSP00000437066.1:n.-221-24C=
ENST00000534644.5:n.494-24C=
ENST00000611494.4:c.509-24C= ENSP00000484546.1:n.509-24C=
NM_000391.3:c.509-24C= NP_000382.3:n.509-24C=
NM_000391.4:c.509-24C= MANE Select NP_000382.3:n.509-24C=