Canonical Allele Identifier: CA472769333

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6635846G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614615G>C , CM000673.2:g.6614615G>C	GRCh38
NC_000011.9:g.6635846G>C , CM000673.1:g.6635846G>C	GRCh37
NC_000011.8:g.6592422G>C	NCBI36
NG_008653.1:g.9847C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1509C>G	ENSP00000507321.1:p.Gly503=
ENST00000299427.12:c.1623C>G MANE Select	ENSP00000299427.6:p.Gly541=
ENST00000524611.2:n.662C>G
ENST00000524924.2:n.743C>G
ENST00000533371.6:c.894C>G	ENSP00000437066.1:p.Gly298=
ENST00000642892.1:c.894C>G	ENSP00000494165.1:p.Gly298=
ENST00000643342.1:c.696C>G
ENST00000643439.1:c.*1363C>G	ENSP00000495849.1:n.*1363C>G
ENST00000643479.1:n.1809C>G
ENST00000643516.1:c.1132C>G
ENST00000644218.1:c.1434C>G	ENSP00000493574.1:p.Gly478=
ENST00000644683.1:c.*1076C>G	ENSP00000494085.1:n.*1076C>G
ENST00000644810.1:c.1344C>G	ENSP00000495895.1:p.Gly448=
ENST00000644831.1:n.1799C>G
ENST00000644933.1:c.*489C>G	ENSP00000496133.1:n.*489C>G
ENST00000645285.1:c.*489C>G	ENSP00000495058.1:n.*489C>G
ENST00000645331.1:n.2828C>G
ENST00000645620.1:c.894C>G	ENSP00000493657.1:p.Gly298=
ENST00000646691.1:n.1510C>G
ENST00000646777.1:n.1956C>G
ENST00000647016.1:n.2103C>G
ENST00000647152.1:c.894C>G	ENSP00000495893.1:p.Gly298=
ENST00000647209.1:c.*1492C>G	ENSP00000495558.1:n.*1492C>G
ENST00000647346.1:n.2643C>G
ENST00000299427.10:c.1623C>G	ENSP00000299427.6:p.Gly541=
ENST00000533371.5:c.894C>G	ENSP00000437066.1:p.Gly298=
ENST00000611494.4:c.1623C>G	ENSP00000484546.1:p.Gly541=
NM_000391.3:c.1623C>G	NP_000382.3:p.Gly541=
NM_000391.4:c.1623C>G MANE Select	NP_000382.3:p.Gly541=