Canonical Allele Identifier: CA1950237693
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616985G= , CM000673.2:g.6616985G= GRCh38
NC_000011.9:g.6638216G= , CM000673.1:g.6638216G= GRCh37
NC_000011.8:g.6594792G= NCBI36
NG_008653.1:g.7477C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.563C= ENSP00000507321.1:p.Ala188=
ENST00000299427.12:c.677C= MANE Select ENSP00000299427.6:p.Ala226=
ENST00000436873.7:c.312+316C=
ENST00000524788.2:n.1836C=
ENST00000524903.2:n.1952C=
ENST00000528807.2:n.333C=
ENST00000530040.2:n.479+374C=
ENST00000533371.6:c.-53C= ENSP00000437066.1:n.-53C=
ENST00000534644.6:n.625C=
ENST00000642892.1:c.-53C= ENSP00000494165.1:n.-53C=
ENST00000643439.1:c.*417C= ENSP00000495849.1:n.*417C=
ENST00000643479.1:n.706C=
ENST00000643516.1:c.395+316C=
ENST00000644151.1:n.2116C=
ENST00000644218.1:c.677C= ENSP00000493574.1:p.Ala226=
ENST00000644683.1:c.*130C= ENSP00000494085.1:n.*130C=
ENST00000644810.1:c.398C= ENSP00000495895.1:p.Ala133=
ENST00000644831.1:n.853C=
ENST00000644933.1:c.-53C= ENSP00000496133.1:n.-53C=
ENST00000645020.1:n.1852C=
ENST00000645285.1:c.-53C= ENSP00000495058.1:n.-53C=
ENST00000645331.1:n.1043C=
ENST00000645620.1:c.-53C= ENSP00000493657.1:n.-53C=
ENST00000646777.1:n.853C=
ENST00000647016.1:n.1157C=
ENST00000647152.1:c.-53C= ENSP00000495893.1:n.-53C=
ENST00000647209.1:c.*546C= ENSP00000495558.1:n.*546C=
ENST00000647346.1:n.1697C=
ENST00000299427.10:c.677C= ENSP00000299427.6:p.Ala226=
ENST00000436873.6:c.450+374C= ENSP00000398136.2:n.450+374C=
ENST00000524788.1:n.377C=
ENST00000528571.5:c.*417C= ENSP00000434647.1:n.*417C=
ENST00000528807.1:n.227C=
ENST00000533371.5:c.-53C= ENSP00000437066.1:n.-53C=
ENST00000611494.4:c.677C= ENSP00000484546.1:p.Ala226=
NM_000391.3:c.677C= NP_000382.3:p.Ala226=
NM_000391.4:c.677C= MANE Select NP_000382.3:p.Ala226=