Canonical Allele Identifier: CA1950232529

Gene: TPP1

Linked Data

• dbSNP Id: rs1564853977

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614540A>G , CM000673.2:g.6614540A>G	GRCh38
NC_000011.9:g.6635771A>G , CM000673.1:g.6635771A>G	GRCh37
NC_000011.8:g.6592347A>G	NCBI36
NG_008653.1:g.9922T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*6T>C	ENSP00000507321.1:n.*6T>C
ENST00000299427.12:c.*6T>C MANE Select	ENSP00000299427.6:n.*6T>C
ENST00000524611.2:n.737T>C
ENST00000533371.6:c.*6T>C	ENSP00000437066.1:n.*6T>C
ENST00000642892.1:c.*6T>C	ENSP00000494165.1:n.*6T>C
ENST00000643342.1:c.771T>C
ENST00000643439.1:c.*1438T>C	ENSP00000495849.1:n.*1438T>C
ENST00000643479.1:n.1884T>C
ENST00000643516.1:c.1207T>C
ENST00000644218.1:c.*6T>C	ENSP00000493574.1:n.*6T>C
ENST00000644683.1:c.*1151T>C	ENSP00000494085.1:n.*1151T>C
ENST00000644810.1:c.*6T>C	ENSP00000495895.1:n.*6T>C
ENST00000644831.1:n.1874T>C
ENST00000644933.1:c.*564T>C	ENSP00000496133.1:n.*564T>C
ENST00000645285.1:c.*564T>C	ENSP00000495058.1:n.*564T>C
ENST00000645331.1:n.2903T>C
ENST00000645620.1:c.*6T>C	ENSP00000493657.1:n.*6T>C
ENST00000646691.1:n.1585T>C
ENST00000646777.1:n.2031T>C
ENST00000647016.1:n.2178T>C
ENST00000647152.1:c.*6T>C	ENSP00000495893.1:n.*6T>C
ENST00000647209.1:c.*1567T>C	ENSP00000495558.1:n.*1567T>C
ENST00000647346.1:n.2718T>C
ENST00000299427.10:c.*6T>C	ENSP00000299427.6:n.*6T>C
ENST00000533371.5:c.*6T>C	ENSP00000437066.1:n.*6T>C
ENST00000611494.4:c.*26T>C	ENSP00000484546.1:n.*26T>C
NM_000391.3:c.*6T>C	NP_000382.3:n.*6T>C
NM_000391.4:c.*6T>C MANE Select	NP_000382.3:n.*6T>C