Canonical Allele Identifier: CA1950237714
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616993G= , CM000673.2:g.6616993G= GRCh38
NC_000011.9:g.6638224G= , CM000673.1:g.6638224G= GRCh37
NC_000011.8:g.6594800G= NCBI36
NG_008653.1:g.7469C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.555C= ENSP00000507321.1:p.Asn185=
ENST00000299427.12:c.669C= MANE Select ENSP00000299427.6:p.Asn223=
ENST00000436873.7:c.312+308C=
ENST00000524788.2:n.1828C=
ENST00000524903.2:n.1944C=
ENST00000528807.2:n.325C=
ENST00000530040.2:n.479+366C=
ENST00000533371.6:c.-61C= ENSP00000437066.1:n.-61C=
ENST00000534644.6:n.617C=
ENST00000642892.1:c.-61C= ENSP00000494165.1:n.-61C=
ENST00000643439.1:c.*409C= ENSP00000495849.1:n.*409C=
ENST00000643479.1:n.698C=
ENST00000643516.1:c.395+308C=
ENST00000644151.1:n.2108C=
ENST00000644218.1:c.669C= ENSP00000493574.1:p.Asn223=
ENST00000644683.1:c.*122C= ENSP00000494085.1:n.*122C=
ENST00000644810.1:c.390C= ENSP00000495895.1:p.Asn130=
ENST00000644831.1:n.845C=
ENST00000644933.1:c.-61C= ENSP00000496133.1:n.-61C=
ENST00000645020.1:n.1844C=
ENST00000645285.1:c.-61C= ENSP00000495058.1:n.-61C=
ENST00000645331.1:n.1035C=
ENST00000645620.1:c.-61C= ENSP00000493657.1:n.-61C=
ENST00000646777.1:n.845C=
ENST00000647016.1:n.1149C=
ENST00000647152.1:c.-61C= ENSP00000495893.1:n.-61C=
ENST00000647209.1:c.*538C= ENSP00000495558.1:n.*538C=
ENST00000647346.1:n.1689C=
ENST00000299427.10:c.669C= ENSP00000299427.6:p.Asn223=
ENST00000428886.6:n.838C=
ENST00000436873.6:c.450+366C= ENSP00000398136.2:n.450+366C=
ENST00000524788.1:n.369C=
ENST00000528571.5:c.*409C= ENSP00000434647.1:n.*409C=
ENST00000528807.1:n.219C=
ENST00000533371.5:c.-61C= ENSP00000437066.1:n.-61C=
ENST00000611494.4:c.669C= ENSP00000484546.1:p.Asn223=
NM_000391.3:c.669C= NP_000382.3:p.Asn223=
NM_000391.4:c.669C= MANE Select NP_000382.3:p.Asn223=