Canonical Allele Identifier: CA379475615

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638360G>T (hg19) ; chr11:g.6617129G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617129G>T , CM000673.2:g.6617129G>T	GRCh38
NC_000011.9:g.6638360G>T , CM000673.1:g.6638360G>T	GRCh37
NC_000011.8:g.6594936G>T	NCBI36
NG_008653.1:g.7333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.419C>A	ENSP00000507321.1:p.Pro140Gln
ENST00000299427.12:c.533C>A MANE Select	ENSP00000299427.6:p.Pro178Gln
ENST00000428886.7:n.768C>A
ENST00000436873.7:c.312+172C>A
ENST00000524788.2:n.1692C>A
ENST00000524903.2:n.1808C>A
ENST00000528807.2:n.189C>A
ENST00000530040.2:n.479+230C>A
ENST00000533371.6:c.-197C>A	ENSP00000437066.1:n.-197C>A
ENST00000534644.6:n.481C>A
ENST00000642892.1:c.-197C>A	ENSP00000494165.1:n.-197C>A
ENST00000643439.1:c.*273C>A	ENSP00000495849.1:n.*273C>A
ENST00000643479.1:n.562C>A
ENST00000643516.1:c.395+172C>A
ENST00000644151.1:n.1972C>A
ENST00000644218.1:c.533C>A	ENSP00000493574.1:p.Pro178Gln
ENST00000644683.1:c.475C>A	ENSP00000494085.1:p.Gln159Lys
ENST00000644810.1:c.254C>A	ENSP00000495895.1:p.Pro85Gln
ENST00000644831.1:n.709C>A
ENST00000644933.1:c.-197C>A	ENSP00000496133.1:n.-197C>A
ENST00000645020.1:n.1708C>A
ENST00000645285.1:c.-197C>A	ENSP00000495058.1:n.-197C>A
ENST00000645331.1:n.899C>A
ENST00000645620.1:c.-197C>A	ENSP00000493657.1:n.-197C>A
ENST00000646777.1:n.709C>A
ENST00000647016.1:n.1013C>A
ENST00000647152.1:c.-197C>A	ENSP00000495893.1:n.-197C>A
ENST00000647209.1:c.*402C>A	ENSP00000495558.1:n.*402C>A
ENST00000647346.1:n.1553C>A
ENST00000299427.10:c.533C>A	ENSP00000299427.6:p.Pro178Gln
ENST00000428886.6:n.702C>A
ENST00000436873.6:c.450+230C>A	ENSP00000398136.2:n.450+230C>A
ENST00000524788.1:n.233C>A
ENST00000528571.5:c.*273C>A	ENSP00000434647.1:n.*273C>A
ENST00000528807.1:n.83C>A
ENST00000533371.5:c.-197C>A	ENSP00000437066.1:n.-197C>A
ENST00000534644.5:n.518C>A
ENST00000611494.4:c.533C>A	ENSP00000484546.1:p.Pro178Gln
NM_000391.3:c.533C>A	NP_000382.3:p.Pro178Gln
NM_000391.4:c.533C>A MANE Select	NP_000382.3:p.Pro178Gln