Canonical Allele Identifier: CA379476051

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638648A>G (hg19) ; chr11:g.6617417A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617417A>G , CM000673.2:g.6617417A>G	GRCh38
NC_000011.9:g.6638648A>G , CM000673.1:g.6638648A>G	GRCh37
NC_000011.8:g.6595224A>G	NCBI36
NG_008653.1:g.7045T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.278T>C	ENSP00000507321.1:p.Leu93Pro
ENST00000299427.12:c.392T>C MANE Select	ENSP00000299427.6:p.Leu131Pro
ENST00000428886.7:n.480T>C
ENST00000436873.7:c.196T>C
ENST00000524788.2:n.1404T>C
ENST00000524903.2:n.1520T>C
ENST00000528571.6:c.*132T>C	ENSP00000434647.1:n.*132T>C
ENST00000528807.2:n.48T>C
ENST00000530040.2:n.421T>C
ENST00000533371.6:c.-338T>C	ENSP00000437066.1:n.-338T>C
ENST00000534644.6:n.393T>C
ENST00000642892.1:c.-285T>C	ENSP00000494165.1:n.-285T>C
ENST00000643439.1:c.*132T>C	ENSP00000495849.1:n.*132T>C
ENST00000643479.1:n.421T>C
ENST00000643516.1:c.279T>C
ENST00000644151.1:n.1684T>C
ENST00000644218.1:c.392T>C	ENSP00000493574.1:p.Leu131Pro
ENST00000644683.1:c.392T>C	ENSP00000494085.1:p.Leu131Pro
ENST00000644810.1:c.230-264T>C	ENSP00000495895.1:n.230-264T>C
ENST00000644831.1:n.421T>C
ENST00000644933.1:c.-338T>C	ENSP00000496133.1:n.-338T>C
ENST00000645020.1:n.1420T>C
ENST00000645285.1:c.-338T>C	ENSP00000495058.1:n.-338T>C
ENST00000645331.1:n.611T>C
ENST00000645620.1:c.-280T>C	ENSP00000493657.1:n.-280T>C
ENST00000646777.1:n.421T>C
ENST00000647016.1:n.725T>C
ENST00000647152.1:c.-338T>C	ENSP00000495893.1:n.-338T>C
ENST00000647209.1:c.*261T>C	ENSP00000495558.1:n.*261T>C
ENST00000647346.1:n.1412T>C
ENST00000299427.10:c.392T>C	ENSP00000299427.6:p.Leu131Pro
ENST00000428886.6:n.414T>C
ENST00000436873.6:c.392T>C	ENSP00000398136.2:p.Leu131Pro
ENST00000528571.5:c.*132T>C	ENSP00000434647.1:n.*132T>C
ENST00000530040.1:n.504T>C
ENST00000533371.5:c.-338T>C	ENSP00000437066.1:n.-338T>C
ENST00000534644.5:n.377T>C
ENST00000611494.4:c.392T>C	ENSP00000484546.1:p.Leu131Pro
NM_000391.3:c.392T>C	NP_000382.3:p.Leu131Pro
NM_000391.4:c.392T>C MANE Select	NP_000382.3:p.Leu131Pro