Canonical Allele Identifier: CA379475588

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638345C>A (hg19) ; chr11:g.6617114C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617114C>A , CM000673.2:g.6617114C>A	GRCh38
NC_000011.9:g.6638345C>A , CM000673.1:g.6638345C>A	GRCh37
NC_000011.8:g.6594921C>A	NCBI36
NG_008653.1:g.7348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.434G>T	ENSP00000507321.1:p.Arg145Met
ENST00000299427.12:c.548G>T MANE Select	ENSP00000299427.6:p.Arg183Met
ENST00000428886.7:n.783G>T
ENST00000436873.7:c.312+187G>T
ENST00000524788.2:n.1707G>T
ENST00000524903.2:n.1823G>T
ENST00000528807.2:n.204G>T
ENST00000530040.2:n.479+245G>T
ENST00000533371.6:c.-182G>T	ENSP00000437066.1:n.-182G>T
ENST00000534644.6:n.496G>T
ENST00000642892.1:c.-182G>T	ENSP00000494165.1:n.-182G>T
ENST00000643439.1:c.*288G>T	ENSP00000495849.1:n.*288G>T
ENST00000643479.1:n.577G>T
ENST00000643516.1:c.395+187G>T
ENST00000644151.1:n.1987G>T
ENST00000644218.1:c.548G>T	ENSP00000493574.1:p.Arg183Met
ENST00000644683.1:c.*1G>T	ENSP00000494085.1:n.*1G>T
ENST00000644810.1:c.269G>T	ENSP00000495895.1:p.Arg90Met
ENST00000644831.1:n.724G>T
ENST00000644933.1:c.-182G>T	ENSP00000496133.1:n.-182G>T
ENST00000645020.1:n.1723G>T
ENST00000645285.1:c.-182G>T	ENSP00000495058.1:n.-182G>T
ENST00000645331.1:n.914G>T
ENST00000645620.1:c.-182G>T	ENSP00000493657.1:n.-182G>T
ENST00000646777.1:n.724G>T
ENST00000647016.1:n.1028G>T
ENST00000647152.1:c.-182G>T	ENSP00000495893.1:n.-182G>T
ENST00000647209.1:c.*417G>T	ENSP00000495558.1:n.*417G>T
ENST00000647346.1:n.1568G>T
ENST00000299427.10:c.548G>T	ENSP00000299427.6:p.Arg183Met
ENST00000428886.6:n.717G>T
ENST00000436873.6:c.450+245G>T	ENSP00000398136.2:n.450+245G>T
ENST00000524788.1:n.248G>T
ENST00000528571.5:c.*288G>T	ENSP00000434647.1:n.*288G>T
ENST00000528807.1:n.98G>T
ENST00000533371.5:c.-182G>T	ENSP00000437066.1:n.-182G>T
ENST00000534644.5:n.533G>T
ENST00000611494.4:c.548G>T	ENSP00000484546.1:p.Arg183Met
NM_000391.3:c.548G>T	NP_000382.3:p.Arg183Met
NM_000391.4:c.548G>T MANE Select	NP_000382.3:p.Arg183Met