Canonical Allele Identifier: CA1950215374
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617745A= , CM000673.2:g.6617745A= GRCh38
NC_000011.9:g.6638976A= , CM000673.1:g.6638976A= GRCh37
NC_000011.8:g.6595552A= NCBI36
NG_008653.1:g.6717T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.147T= ENSP00000507321.1:p.Asp49=
ENST00000299427.12:c.261T= MANE Select ENSP00000299427.6:p.Asp87=
ENST00000428886.7:n.349T=
ENST00000436873.7:c.65T=
ENST00000524788.2:n.1273T=
ENST00000524903.2:n.1389T=
ENST00000528571.6:c.*1T= ENSP00000434647.1:n.*1T=
ENST00000530040.2:n.290T=
ENST00000533371.6:c.-469T= ENSP00000437066.1:n.-469T=
ENST00000534644.6:n.262T=
ENST00000642892.1:c.-416T= ENSP00000494165.1:n.-416T=
ENST00000643439.1:c.*1T= ENSP00000495849.1:n.*1T=
ENST00000643479.1:n.290T=
ENST00000643516.1:c.148T=
ENST00000644151.1:n.1553T=
ENST00000644218.1:c.261T= ENSP00000493574.1:p.Asp87=
ENST00000644683.1:c.261T= ENSP00000494085.1:p.Asp87=
ENST00000644810.1:c.230-592T= ENSP00000495895.1:n.230-592T=
ENST00000644831.1:n.290T=
ENST00000644933.1:c.-469T= ENSP00000496133.1:n.-469T=
ENST00000645020.1:n.1289T=
ENST00000645285.1:c.-469T= ENSP00000495058.1:n.-469T=
ENST00000645331.1:n.283T=
ENST00000645620.1:c.-411T= ENSP00000493657.1:n.-411T=
ENST00000646777.1:n.290T=
ENST00000647016.1:n.594T=
ENST00000647152.1:c.-469T= ENSP00000495893.1:n.-469T=
ENST00000647209.1:c.*130T= ENSP00000495558.1:n.*130T=
ENST00000647346.1:n.1281T=
ENST00000299427.10:c.261T= ENSP00000299427.6:p.Asp87=
ENST00000428886.6:n.283T=
ENST00000436873.6:c.261T= ENSP00000398136.2:p.Asp87=
ENST00000528571.5:c.*1T= ENSP00000434647.1:n.*1T=
ENST00000530040.1:n.373T=
ENST00000533371.5:c.-469T= ENSP00000437066.1:n.-469T=
ENST00000534644.5:n.246T=
ENST00000611494.4:c.261T= ENSP00000484546.1:p.Asp87=
NM_000391.3:c.261T= NP_000382.3:p.Asp87=
NM_000391.4:c.261T= MANE Select NP_000382.3:p.Asp87=