Canonical Allele Identifier: CA472922927

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638281C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617050C>A , CM000673.2:g.6617050C>A	GRCh38
NC_000011.9:g.6638281C>A , CM000673.1:g.6638281C>A	GRCh37
NC_000011.8:g.6594857C>A	NCBI36
NG_008653.1:g.7412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.498G>T	ENSP00000507321.1:p.Val166=
ENST00000299427.12:c.612G>T MANE Select	ENSP00000299427.6:p.Val204=
ENST00000436873.7:c.312+251G>T
ENST00000524788.2:n.1771G>T
ENST00000524903.2:n.1887G>T
ENST00000528807.2:n.268G>T
ENST00000530040.2:n.479+309G>T
ENST00000533371.6:c.-118G>T	ENSP00000437066.1:n.-118G>T
ENST00000534644.6:n.560G>T
ENST00000642892.1:c.-118G>T	ENSP00000494165.1:n.-118G>T
ENST00000643439.1:c.*352G>T	ENSP00000495849.1:n.*352G>T
ENST00000643479.1:n.641G>T
ENST00000643516.1:c.395+251G>T
ENST00000644151.1:n.2051G>T
ENST00000644218.1:c.612G>T	ENSP00000493574.1:p.Val204=
ENST00000644683.1:c.*65G>T	ENSP00000494085.1:n.*65G>T
ENST00000644810.1:c.333G>T	ENSP00000495895.1:p.Val111=
ENST00000644831.1:n.788G>T
ENST00000644933.1:c.-118G>T	ENSP00000496133.1:n.-118G>T
ENST00000645020.1:n.1787G>T
ENST00000645285.1:c.-118G>T	ENSP00000495058.1:n.-118G>T
ENST00000645331.1:n.978G>T
ENST00000645620.1:c.-118G>T	ENSP00000493657.1:n.-118G>T
ENST00000646777.1:n.788G>T
ENST00000647016.1:n.1092G>T
ENST00000647152.1:c.-118G>T	ENSP00000495893.1:n.-118G>T
ENST00000647209.1:c.*481G>T	ENSP00000495558.1:n.*481G>T
ENST00000647346.1:n.1632G>T
ENST00000299427.10:c.612G>T	ENSP00000299427.6:p.Val204=
ENST00000428886.6:n.781G>T
ENST00000436873.6:c.450+309G>T	ENSP00000398136.2:n.450+309G>T
ENST00000524788.1:n.312G>T
ENST00000528571.5:c.*352G>T	ENSP00000434647.1:n.*352G>T
ENST00000528807.1:n.162G>T
ENST00000533371.5:c.-118G>T	ENSP00000437066.1:n.-118G>T
ENST00000534644.5:n.597G>T
ENST00000611494.4:c.612G>T	ENSP00000484546.1:p.Val204=
NM_000391.3:c.612G>T	NP_000382.3:p.Val204=
NM_000391.4:c.612G>T MANE Select	NP_000382.3:p.Val204=