Canonical Allele Identifier: CA2612256362

Gene: TPP1

Linked Data

• gnomAD v4: 11-6614538-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614538G>C , CM000673.2:g.6614538G>C	GRCh38
NC_000011.9:g.6635769G>C , CM000673.1:g.6635769G>C	GRCh37
NC_000011.8:g.6592345G>C	NCBI36
NG_008653.1:g.9924C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*8C>G	ENSP00000507321.1:n.*8C>G
ENST00000299427.12:c.*8C>G MANE Select	ENSP00000299427.6:n.*8C>G
ENST00000524611.2:n.739C>G
ENST00000533371.6:c.*8C>G	ENSP00000437066.1:n.*8C>G
ENST00000642892.1:c.*8C>G	ENSP00000494165.1:n.*8C>G
ENST00000643342.1:c.773C>G
ENST00000643439.1:c.*1440C>G	ENSP00000495849.1:n.*1440C>G
ENST00000643479.1:n.1886C>G
ENST00000643516.1:c.1209C>G
ENST00000644218.1:c.*8C>G	ENSP00000493574.1:n.*8C>G
ENST00000644683.1:c.*1153C>G	ENSP00000494085.1:n.*1153C>G
ENST00000644810.1:c.*8C>G	ENSP00000495895.1:n.*8C>G
ENST00000644831.1:n.1876C>G
ENST00000644933.1:c.*566C>G	ENSP00000496133.1:n.*566C>G
ENST00000645285.1:c.*566C>G	ENSP00000495058.1:n.*566C>G
ENST00000645331.1:n.2905C>G
ENST00000645620.1:c.*8C>G	ENSP00000493657.1:n.*8C>G
ENST00000646691.1:n.1587C>G
ENST00000646777.1:n.2033C>G
ENST00000647016.1:n.2180C>G
ENST00000647152.1:c.*8C>G	ENSP00000495893.1:n.*8C>G
ENST00000647209.1:c.*1569C>G	ENSP00000495558.1:n.*1569C>G
ENST00000647346.1:n.2720C>G
ENST00000299427.10:c.*8C>G	ENSP00000299427.6:n.*8C>G
ENST00000533371.5:c.*8C>G	ENSP00000437066.1:n.*8C>G
ENST00000611494.4:c.*28C>G	ENSP00000484546.1:n.*28C>G
NM_000391.3:c.*8C>G	NP_000382.3:n.*8C>G
NM_000391.4:c.*8C>G MANE Select	NP_000382.3:n.*8C>G