Canonical Allele Identifier: CA379476168
Gene: TPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617639A>T , CM000673.2:g.6617639A>T GRCh38
NC_000011.9:g.6638870A>T , CM000673.1:g.6638870A>T GRCh37
NC_000011.8:g.6595446A>T NCBI36
NG_008653.1:g.6823T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.253T>A ENSP00000507321.1:p.Trp85Arg
ENST00000299427.12:c.367T>A MANE Select ENSP00000299427.6:p.Trp123Arg
ENST00000428886.7:n.455T>A
ENST00000436873.7:c.171T>A
ENST00000524788.2:n.1379T>A
ENST00000524903.2:n.1495T>A
ENST00000528571.6:c.*107T>A ENSP00000434647.1:n.*107T>A
ENST00000530040.2:n.396T>A
ENST00000533371.6:c.-363T>A ENSP00000437066.1:n.-363T>A
ENST00000534644.6:n.368T>A
ENST00000642892.1:c.-310T>A ENSP00000494165.1:n.-310T>A
ENST00000643439.1:c.*107T>A ENSP00000495849.1:n.*107T>A
ENST00000643479.1:n.396T>A
ENST00000643516.1:c.254T>A
ENST00000644151.1:n.1659T>A
ENST00000644218.1:c.367T>A ENSP00000493574.1:p.Trp123Arg
ENST00000644683.1:c.367T>A ENSP00000494085.1:p.Trp123Arg
ENST00000644810.1:c.230-486T>A ENSP00000495895.1:n.230-486T>A
ENST00000644831.1:n.396T>A
ENST00000644933.1:c.-363T>A ENSP00000496133.1:n.-363T>A
ENST00000645020.1:n.1395T>A
ENST00000645285.1:c.-363T>A ENSP00000495058.1:n.-363T>A
ENST00000645331.1:n.389T>A
ENST00000645620.1:c.-305T>A ENSP00000493657.1:n.-305T>A
ENST00000646777.1:n.396T>A
ENST00000647016.1:n.700T>A
ENST00000647152.1:c.-363T>A ENSP00000495893.1:n.-363T>A
ENST00000647209.1:c.*236T>A ENSP00000495558.1:n.*236T>A
ENST00000647346.1:n.1387T>A
ENST00000299427.10:c.367T>A ENSP00000299427.6:p.Trp123Arg
ENST00000428886.6:n.389T>A
ENST00000436873.6:c.367T>A ENSP00000398136.2:p.Trp123Arg
ENST00000528571.5:c.*107T>A ENSP00000434647.1:n.*107T>A
ENST00000530040.1:n.479T>A
ENST00000533371.5:c.-363T>A ENSP00000437066.1:n.-363T>A
ENST00000534644.5:n.352T>A
ENST00000611494.4:c.367T>A ENSP00000484546.1:p.Trp123Arg
NM_000391.3:c.367T>A NP_000382.3:p.Trp123Arg
NM_000391.4:c.367T>A MANE Select NP_000382.3:p.Trp123Arg