Canonical Allele Identifier: CA472922889

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638536G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617305G>A , CM000673.2:g.6617305G>A	GRCh38
NC_000011.9:g.6638536G>A , CM000673.1:g.6638536G>A	GRCh37
NC_000011.8:g.6595112G>A	NCBI36
NG_008653.1:g.7157C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.390C>T	ENSP00000507321.1:p.Asp130=
ENST00000299427.12:c.504C>T MANE Select	ENSP00000299427.6:p.Asp168=
ENST00000428886.7:n.592C>T
ENST00000436873.7:c.308C>T
ENST00000524788.2:n.1516C>T
ENST00000524903.2:n.1632C>T
ENST00000528571.6:c.*244C>T	ENSP00000434647.1:n.*244C>T
ENST00000528807.2:n.160C>T
ENST00000530040.2:n.479+54C>T
ENST00000533371.6:c.-226C>T	ENSP00000437066.1:n.-226C>T
ENST00000534644.6:n.456+49C>T
ENST00000642892.1:c.-222+49C>T	ENSP00000494165.1:n.-222+49C>T
ENST00000643439.1:c.*244C>T	ENSP00000495849.1:n.*244C>T
ENST00000643479.1:n.533C>T
ENST00000643516.1:c.391C>T
ENST00000644151.1:n.1796C>T
ENST00000644218.1:c.504C>T	ENSP00000493574.1:p.Asp168=
ENST00000644683.1:c.450+54C>T	ENSP00000494085.1:n.450+54C>T
ENST00000644810.1:c.230-152C>T	ENSP00000495895.1:n.230-152C>T
ENST00000644831.1:n.533C>T
ENST00000644933.1:c.-226C>T	ENSP00000496133.1:n.-226C>T
ENST00000645020.1:n.1532C>T
ENST00000645285.1:c.-226C>T	ENSP00000495058.1:n.-226C>T
ENST00000645331.1:n.723C>T
ENST00000645620.1:c.-222+54C>T	ENSP00000493657.1:n.-222+54C>T
ENST00000646777.1:n.533C>T
ENST00000647016.1:n.837C>T
ENST00000647152.1:c.-226C>T	ENSP00000495893.1:n.-226C>T
ENST00000647209.1:c.*373C>T	ENSP00000495558.1:n.*373C>T
ENST00000647346.1:n.1524C>T
ENST00000299427.10:c.504C>T	ENSP00000299427.6:p.Asp168=
ENST00000428886.6:n.526C>T
ENST00000436873.6:c.450+54C>T	ENSP00000398136.2:n.450+54C>T
ENST00000524788.1:n.57C>T
ENST00000528571.5:c.*244C>T	ENSP00000434647.1:n.*244C>T
ENST00000533371.5:c.-226C>T	ENSP00000437066.1:n.-226C>T
ENST00000534644.5:n.489C>T
ENST00000611494.4:c.504C>T	ENSP00000484546.1:p.Asp168=
NM_000391.3:c.504C>T	NP_000382.3:p.Asp168=
NM_000391.4:c.504C>T MANE Select	NP_000382.3:p.Asp168=