Canonical Allele Identifier: CA2612256364

Gene: TPP1

Linked Data

• gnomAD v4: 11-6614544-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614544G>T , CM000673.2:g.6614544G>T	GRCh38
NC_000011.9:g.6635775G>T , CM000673.1:g.6635775G>T	GRCh37
NC_000011.8:g.6592351G>T	NCBI36
NG_008653.1:g.9918C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*2C>A	ENSP00000507321.1:n.*2C>A
ENST00000299427.12:c.*2C>A MANE Select	ENSP00000299427.6:n.*2C>A
ENST00000524611.2:n.733C>A
ENST00000533371.6:c.*2C>A	ENSP00000437066.1:n.*2C>A
ENST00000642892.1:c.*2C>A	ENSP00000494165.1:n.*2C>A
ENST00000643342.1:c.767C>A
ENST00000643439.1:c.*1434C>A	ENSP00000495849.1:n.*1434C>A
ENST00000643479.1:n.1880C>A
ENST00000643516.1:c.1203C>A
ENST00000644218.1:c.*2C>A	ENSP00000493574.1:n.*2C>A
ENST00000644683.1:c.*1147C>A	ENSP00000494085.1:n.*1147C>A
ENST00000644810.1:c.*2C>A	ENSP00000495895.1:n.*2C>A
ENST00000644831.1:n.1870C>A
ENST00000644933.1:c.*560C>A	ENSP00000496133.1:n.*560C>A
ENST00000645285.1:c.*560C>A	ENSP00000495058.1:n.*560C>A
ENST00000645331.1:n.2899C>A
ENST00000645620.1:c.*2C>A	ENSP00000493657.1:n.*2C>A
ENST00000646691.1:n.1581C>A
ENST00000646777.1:n.2027C>A
ENST00000647016.1:n.2174C>A
ENST00000647152.1:c.*2C>A	ENSP00000495893.1:n.*2C>A
ENST00000647209.1:c.*1563C>A	ENSP00000495558.1:n.*1563C>A
ENST00000647346.1:n.2714C>A
ENST00000299427.10:c.*2C>A	ENSP00000299427.6:n.*2C>A
ENST00000533371.5:c.*2C>A	ENSP00000437066.1:n.*2C>A
ENST00000611494.4:c.*22C>A	ENSP00000484546.1:n.*22C>A
NM_000391.3:c.*2C>A	NP_000382.3:n.*2C>A
NM_000391.4:c.*2C>A MANE Select	NP_000382.3:n.*2C>A