Canonical Allele Identifier: CA379475074

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637993C>A (hg19) ; chr11:g.6616762C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616762C>A , CM000673.2:g.6616762C>A	GRCh38
NC_000011.9:g.6637993C>A , CM000673.1:g.6637993C>A	GRCh37
NC_000011.8:g.6594569C>A	NCBI36
NG_008653.1:g.7700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.671G>T	ENSP00000507321.1:p.Gly224Val
ENST00000299427.12:c.785G>T MANE Select	ENSP00000299427.6:p.Gly262Val
ENST00000436873.7:c.312+539G>T
ENST00000524788.2:n.1944G>T
ENST00000524903.2:n.2060G>T
ENST00000528807.2:n.441G>T
ENST00000530040.2:n.480-259G>T
ENST00000533371.6:c.56G>T	ENSP00000437066.1:p.Gly19Val
ENST00000642892.1:c.56G>T	ENSP00000494165.1:p.Gly19Val
ENST00000643439.1:c.*525G>T	ENSP00000495849.1:n.*525G>T
ENST00000643479.1:n.814G>T
ENST00000643516.1:c.396-259G>T
ENST00000644151.1:n.2224G>T
ENST00000644218.1:c.785G>T	ENSP00000493574.1:p.Gly262Val
ENST00000644683.1:c.*238G>T	ENSP00000494085.1:n.*238G>T
ENST00000644810.1:c.506G>T	ENSP00000495895.1:p.Gly169Val
ENST00000644831.1:n.961G>T
ENST00000644933.1:c.56G>T	ENSP00000496133.1:p.Gly19Val
ENST00000645020.1:n.2075G>T
ENST00000645285.1:c.56G>T	ENSP00000495058.1:p.Gly19Val
ENST00000645331.1:n.1151G>T
ENST00000645620.1:c.56G>T	ENSP00000493657.1:p.Gly19Val
ENST00000646777.1:n.961G>T
ENST00000647016.1:n.1265G>T
ENST00000647152.1:c.56G>T	ENSP00000495893.1:p.Gly19Val
ENST00000647209.1:c.*654G>T	ENSP00000495558.1:n.*654G>T
ENST00000647346.1:n.1805G>T
ENST00000299427.10:c.785G>T	ENSP00000299427.6:p.Gly262Val
ENST00000436873.6:c.451-259G>T	ENSP00000398136.2:n.451-259G>T
ENST00000524788.1:n.485G>T
ENST00000528807.1:n.335G>T
ENST00000533371.5:c.56G>T	ENSP00000437066.1:p.Gly19Val
ENST00000611494.4:c.785G>T	ENSP00000484546.1:p.Gly262Val
NM_000391.3:c.785G>T	NP_000382.3:p.Gly262Val
NM_000391.4:c.785G>T MANE Select	NP_000382.3:p.Gly262Val