Canonical Allele Identifier: CA379475786

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638573G>C (hg19) ; chr11:g.6617342G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617342G>C , CM000673.2:g.6617342G>C	GRCh38
NC_000011.9:g.6638573G>C , CM000673.1:g.6638573G>C	GRCh37
NC_000011.8:g.6595149G>C	NCBI36
NG_008653.1:g.7120C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.353C>G	ENSP00000507321.1:p.Pro118Arg
ENST00000299427.12:c.467C>G MANE Select	ENSP00000299427.6:p.Pro156Arg
ENST00000428886.7:n.555C>G
ENST00000436873.7:c.271C>G
ENST00000524788.2:n.1479C>G
ENST00000524903.2:n.1595C>G
ENST00000528571.6:c.*207C>G	ENSP00000434647.1:n.*207C>G
ENST00000528807.2:n.123C>G
ENST00000530040.2:n.479+17C>G
ENST00000533371.6:c.-263C>G	ENSP00000437066.1:n.-263C>G
ENST00000534644.6:n.456+12C>G
ENST00000642892.1:c.-222+12C>G	ENSP00000494165.1:n.-222+12C>G
ENST00000643439.1:c.*207C>G	ENSP00000495849.1:n.*207C>G
ENST00000643479.1:n.496C>G
ENST00000643516.1:c.354C>G
ENST00000644151.1:n.1759C>G
ENST00000644218.1:c.467C>G	ENSP00000493574.1:p.Pro156Arg
ENST00000644683.1:c.450+17C>G	ENSP00000494085.1:n.450+17C>G
ENST00000644810.1:c.230-189C>G	ENSP00000495895.1:n.230-189C>G
ENST00000644831.1:n.496C>G
ENST00000644933.1:c.-263C>G	ENSP00000496133.1:n.-263C>G
ENST00000645020.1:n.1495C>G
ENST00000645285.1:c.-263C>G	ENSP00000495058.1:n.-263C>G
ENST00000645331.1:n.686C>G
ENST00000645620.1:c.-222+17C>G	ENSP00000493657.1:n.-222+17C>G
ENST00000646777.1:n.496C>G
ENST00000647016.1:n.800C>G
ENST00000647152.1:c.-263C>G	ENSP00000495893.1:n.-263C>G
ENST00000647209.1:c.*336C>G	ENSP00000495558.1:n.*336C>G
ENST00000647346.1:n.1487C>G
ENST00000299427.10:c.467C>G	ENSP00000299427.6:p.Pro156Arg
ENST00000428886.6:n.489C>G
ENST00000436873.6:c.450+17C>G	ENSP00000398136.2:n.450+17C>G
ENST00000524788.1:n.20C>G
ENST00000528571.5:c.*207C>G	ENSP00000434647.1:n.*207C>G
ENST00000533371.5:c.-263C>G	ENSP00000437066.1:n.-263C>G
ENST00000534644.5:n.452C>G
ENST00000611494.4:c.467C>G	ENSP00000484546.1:p.Pro156Arg
NM_000391.3:c.467C>G	NP_000382.3:p.Pro156Arg
NM_000391.4:c.467C>G MANE Select	NP_000382.3:p.Pro156Arg