Canonical Allele Identifier: CA1950238338
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617259G= , CM000673.2:g.6617259G= GRCh38
NC_000011.9:g.6638490G= , CM000673.1:g.6638490G= GRCh37
NC_000011.8:g.6595066G= NCBI36
NG_008653.1:g.7203C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.394+42C= ENSP00000507321.1:n.394+42C=
ENST00000299427.12:c.508+42C= MANE Select ENSP00000299427.6:n.508+42C=
ENST00000428886.7:n.638C=
ENST00000436873.7:c.312+42C=
ENST00000524788.2:n.1562C=
ENST00000524903.2:n.1678C=
ENST00000528571.6:c.*290C= ENSP00000434647.1:n.*290C=
ENST00000528807.2:n.164+42C=
ENST00000530040.2:n.479+100C=
ENST00000533371.6:c.-222+42C= ENSP00000437066.1:n.-222+42C=
ENST00000534644.6:n.456+95C=
ENST00000642892.1:c.-222+95C= ENSP00000494165.1:n.-222+95C=
ENST00000643439.1:c.*248+42C= ENSP00000495849.1:n.*248+42C=
ENST00000643479.1:n.537+42C=
ENST00000643516.1:c.395+42C=
ENST00000644151.1:n.1842C=
ENST00000644218.1:c.508+42C= ENSP00000493574.1:n.508+42C=
ENST00000644683.1:c.450+100C= ENSP00000494085.1:n.450+100C=
ENST00000644810.1:c.230-106C= ENSP00000495895.1:n.230-106C=
ENST00000644831.1:n.579C=
ENST00000644933.1:c.-222+42C= ENSP00000496133.1:n.-222+42C=
ENST00000645020.1:n.1578C=
ENST00000645285.1:c.-222+42C= ENSP00000495058.1:n.-222+42C=
ENST00000645331.1:n.769C=
ENST00000645620.1:c.-222+100C= ENSP00000493657.1:n.-222+100C=
ENST00000646777.1:n.579C=
ENST00000647016.1:n.883C=
ENST00000647152.1:c.-222+42C= ENSP00000495893.1:n.-222+42C=
ENST00000647209.1:c.*377+42C= ENSP00000495558.1:n.*377+42C=
ENST00000647346.1:n.1528+42C=
ENST00000299427.10:c.508+42C= ENSP00000299427.6:n.508+42C=
ENST00000428886.6:n.572C=
ENST00000436873.6:c.450+100C= ENSP00000398136.2:n.450+100C=
ENST00000524788.1:n.103C=
ENST00000528571.5:c.*248+42C= ENSP00000434647.1:n.*248+42C=
ENST00000533371.5:c.-222+42C= ENSP00000437066.1:n.-222+42C=
ENST00000534644.5:n.493+42C=
ENST00000611494.4:c.508+42C= ENSP00000484546.1:n.508+42C=
NM_000391.3:c.508+42C= NP_000382.3:n.508+42C=
NM_000391.4:c.508+42C= MANE Select NP_000382.3:n.508+42C=