Canonical Allele Identifier: CA379474449

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637674G>C (hg19) ; chr11:g.6616443G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616443G>C , CM000673.2:g.6616443G>C	GRCh38
NC_000011.9:g.6637674G>C , CM000673.1:g.6637674G>C	GRCh37
NC_000011.8:g.6594250G>C	NCBI36
NG_008653.1:g.8019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.833C>G	ENSP00000507321.1:p.Ala278Gly
ENST00000299427.12:c.947C>G MANE Select	ENSP00000299427.6:p.Ala316Gly
ENST00000436873.7:c.313-369C>G
ENST00000530040.2:n.540C>G
ENST00000533371.6:c.218C>G	ENSP00000437066.1:p.Ala73Gly
ENST00000642892.1:c.218C>G	ENSP00000494165.1:p.Ala73Gly
ENST00000643342.1:c.37C>G
ENST00000643439.1:c.*687C>G	ENSP00000495849.1:n.*687C>G
ENST00000643479.1:n.1133C>G
ENST00000643516.1:c.456C>G
ENST00000644218.1:c.886+218C>G	ENSP00000493574.1:n.886+218C>G
ENST00000644683.1:c.*400C>G	ENSP00000494085.1:n.*400C>G
ENST00000644810.1:c.668C>G	ENSP00000495895.1:p.Ala223Gly
ENST00000644831.1:n.1123C>G
ENST00000644933.1:c.218C>G	ENSP00000496133.1:p.Ala73Gly
ENST00000645285.1:c.157+218C>G	ENSP00000495058.1:n.157+218C>G
ENST00000645331.1:n.1470C>G
ENST00000645620.1:c.218C>G	ENSP00000493657.1:p.Ala73Gly
ENST00000646691.1:n.40C>G
ENST00000646777.1:n.1280C>G
ENST00000647016.1:n.1427C>G
ENST00000647152.1:c.218C>G	ENSP00000495893.1:p.Ala73Gly
ENST00000647209.1:c.*816C>G	ENSP00000495558.1:n.*816C>G
ENST00000647346.1:n.1967C>G
ENST00000299427.10:c.947C>G	ENSP00000299427.6:p.Ala316Gly
ENST00000436873.6:c.511C>G	ENSP00000398136.2:p.Pro171Ala
ENST00000533371.5:c.218C>G	ENSP00000437066.1:p.Ala73Gly
ENST00000611494.4:c.947C>G	ENSP00000484546.1:p.Ala316Gly
NM_000391.3:c.947C>G	NP_000382.3:p.Ala316Gly
NM_000391.4:c.947C>G MANE Select	NP_000382.3:p.Ala316Gly