Canonical Allele Identifier: CA379475521
Gene: TPP1 HGNC NCBI

Linked Data

gnomAD v4: 11-6617082-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617082C>A , CM000673.2:g.6617082C>A GRCh38
NC_000011.9:g.6638313C>A , CM000673.1:g.6638313C>A GRCh37
NC_000011.8:g.6594889C>A NCBI36
NG_008653.1:g.7380G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.466G>T ENSP00000507321.1:p.Val156Leu
ENST00000299427.12:c.580G>T MANE Select ENSP00000299427.6:p.Val194Leu
ENST00000428886.7:n.815G>T
ENST00000436873.7:c.312+219G>T
ENST00000524788.2:n.1739G>T
ENST00000524903.2:n.1855G>T
ENST00000528807.2:n.236G>T
ENST00000530040.2:n.479+277G>T
ENST00000533371.6:c.-150G>T ENSP00000437066.1:n.-150G>T
ENST00000534644.6:n.528G>T
ENST00000642892.1:c.-150G>T ENSP00000494165.1:n.-150G>T
ENST00000643439.1:c.*320G>T ENSP00000495849.1:n.*320G>T
ENST00000643479.1:n.609G>T
ENST00000643516.1:c.395+219G>T
ENST00000644151.1:n.2019G>T
ENST00000644218.1:c.580G>T ENSP00000493574.1:p.Val194Leu
ENST00000644683.1:c.*33G>T ENSP00000494085.1:n.*33G>T
ENST00000644810.1:c.301G>T ENSP00000495895.1:p.Val101Leu
ENST00000644831.1:n.756G>T
ENST00000644933.1:c.-150G>T ENSP00000496133.1:n.-150G>T
ENST00000645020.1:n.1755G>T
ENST00000645285.1:c.-150G>T ENSP00000495058.1:n.-150G>T
ENST00000645331.1:n.946G>T
ENST00000645620.1:c.-150G>T ENSP00000493657.1:n.-150G>T
ENST00000646777.1:n.756G>T
ENST00000647016.1:n.1060G>T
ENST00000647152.1:c.-150G>T ENSP00000495893.1:n.-150G>T
ENST00000647209.1:c.*449G>T ENSP00000495558.1:n.*449G>T
ENST00000647346.1:n.1600G>T
ENST00000299427.10:c.580G>T ENSP00000299427.6:p.Val194Leu
ENST00000428886.6:n.749G>T
ENST00000436873.6:c.450+277G>T ENSP00000398136.2:n.450+277G>T
ENST00000524788.1:n.280G>T
ENST00000528571.5:c.*320G>T ENSP00000434647.1:n.*320G>T
ENST00000528807.1:n.130G>T
ENST00000533371.5:c.-150G>T ENSP00000437066.1:n.-150G>T
ENST00000534644.5:n.565G>T
ENST00000611494.4:c.580G>T ENSP00000484546.1:p.Val194Leu
NM_000391.3:c.580G>T NP_000382.3:p.Val194Leu
NM_000391.4:c.580G>T MANE Select NP_000382.3:p.Val194Leu