Canonical Allele Identifier: CA472922862
Gene: TPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1163311968
gnomAD v2: 11-6638376-G-A
gnomAD v4: 11-6617145-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617145G>A , CM000673.2:g.6617145G>A GRCh38
NC_000011.9:g.6638376G>A , CM000673.1:g.6638376G>A GRCh37
NC_000011.8:g.6594952G>A NCBI36
NG_008653.1:g.7317C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.403C>T ENSP00000507321.1:p.Leu135=
ENST00000299427.12:c.517C>T MANE Select ENSP00000299427.6:p.Leu173=
ENST00000428886.7:n.752C>T
ENST00000436873.7:c.312+156C>T
ENST00000524788.2:n.1676C>T
ENST00000524903.2:n.1792C>T
ENST00000528807.2:n.173C>T
ENST00000530040.2:n.479+214C>T
ENST00000533371.6:c.-213C>T ENSP00000437066.1:n.-213C>T
ENST00000534644.6:n.465C>T
ENST00000642892.1:c.-213C>T ENSP00000494165.1:n.-213C>T
ENST00000643439.1:c.*257C>T ENSP00000495849.1:n.*257C>T
ENST00000643479.1:n.546C>T
ENST00000643516.1:c.395+156C>T
ENST00000644151.1:n.1956C>T
ENST00000644218.1:c.517C>T ENSP00000493574.1:p.Leu173=
ENST00000644683.1:c.459C>T ENSP00000494085.1:p.Asp153=
ENST00000644810.1:c.238C>T ENSP00000495895.1:p.Leu80=
ENST00000644831.1:n.693C>T
ENST00000644933.1:c.-213C>T ENSP00000496133.1:n.-213C>T
ENST00000645020.1:n.1692C>T
ENST00000645285.1:c.-213C>T ENSP00000495058.1:n.-213C>T
ENST00000645331.1:n.883C>T
ENST00000645620.1:c.-213C>T ENSP00000493657.1:n.-213C>T
ENST00000646777.1:n.693C>T
ENST00000647016.1:n.997C>T
ENST00000647152.1:c.-213C>T ENSP00000495893.1:n.-213C>T
ENST00000647209.1:c.*386C>T ENSP00000495558.1:n.*386C>T
ENST00000647346.1:n.1537C>T
ENST00000299427.10:c.517C>T ENSP00000299427.6:p.Leu173=
ENST00000428886.6:n.686C>T
ENST00000436873.6:c.450+214C>T ENSP00000398136.2:n.450+214C>T
ENST00000524788.1:n.217C>T
ENST00000528571.5:c.*257C>T ENSP00000434647.1:n.*257C>T
ENST00000528807.1:n.67C>T
ENST00000533371.5:c.-213C>T ENSP00000437066.1:n.-213C>T
ENST00000534644.5:n.502C>T
ENST00000611494.4:c.517C>T ENSP00000484546.1:p.Leu173=
NM_000391.3:c.517C>T NP_000382.3:p.Leu173=
NM_000391.4:c.517C>T MANE Select NP_000382.3:p.Leu173=