Canonical Allele Identifier: CA1950232439

Gene: TPP1

Linked Data

• dbSNP Id: rs1855543936
• gnomAD v4: 11-6614477-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614477G>A , CM000673.2:g.6614477G>A	GRCh38
NC_000011.9:g.6635708G>A , CM000673.1:g.6635708G>A	GRCh37
NC_000011.8:g.6592284G>A	NCBI36
NG_008653.1:g.9985C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*69C>T	ENSP00000507321.1:n.*69C>T
ENST00000299427.12:c.*69C>T MANE Select	ENSP00000299427.6:n.*69C>T
ENST00000524611.2:n.800C>T
ENST00000533371.6:c.*69C>T	ENSP00000437066.1:n.*69C>T
ENST00000642892.1:c.*69C>T	ENSP00000494165.1:n.*69C>T
ENST00000643342.1:c.834C>T
ENST00000643439.1:c.*1501C>T	ENSP00000495849.1:n.*1501C>T
ENST00000643479.1:n.1947C>T
ENST00000643516.1:c.1270C>T
ENST00000644218.1:c.*69C>T	ENSP00000493574.1:n.*69C>T
ENST00000644683.1:c.*1214C>T	ENSP00000494085.1:n.*1214C>T
ENST00000644810.1:c.*69C>T	ENSP00000495895.1:n.*69C>T
ENST00000644831.1:n.1937C>T
ENST00000644933.1:c.*627C>T	ENSP00000496133.1:n.*627C>T
ENST00000645285.1:c.*627C>T	ENSP00000495058.1:n.*627C>T
ENST00000645331.1:n.2966C>T
ENST00000645620.1:c.*69C>T	ENSP00000493657.1:n.*69C>T
ENST00000646691.1:n.1648C>T
ENST00000646777.1:n.2094C>T
ENST00000647016.1:n.2241C>T
ENST00000647152.1:c.*69C>T	ENSP00000495893.1:n.*69C>T
ENST00000647209.1:c.*1630C>T	ENSP00000495558.1:n.*1630C>T
ENST00000647346.1:n.2781C>T
ENST00000299427.10:c.*69C>T	ENSP00000299427.6:n.*69C>T
ENST00000533371.5:c.*69C>T	ENSP00000437066.1:n.*69C>T
ENST00000611494.4:c.*89C>T	ENSP00000484546.1:n.*89C>T
NM_000391.3:c.*69C>T	NP_000382.3:n.*69C>T
NM_000391.4:c.*69C>T MANE Select	NP_000382.3:n.*69C>T