Canonical Allele Identifier: CA1950237255
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616739C= , CM000673.2:g.6616739C= GRCh38
NC_000011.9:g.6637970C= , CM000673.1:g.6637970C= GRCh37
NC_000011.8:g.6594546C= NCBI36
NG_008653.1:g.7723G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.694G= ENSP00000507321.1:p.Gly232=
ENST00000299427.12:c.808G= MANE Select ENSP00000299427.6:p.Gly270=
ENST00000436873.7:c.312+562G=
ENST00000524788.2:n.1967G=
ENST00000524903.2:n.2083G=
ENST00000528807.2:n.464G=
ENST00000530040.2:n.480-236G=
ENST00000533371.6:c.79G= ENSP00000437066.1:p.Gly27=
ENST00000642892.1:c.79G= ENSP00000494165.1:p.Gly27=
ENST00000643439.1:c.*548G= ENSP00000495849.1:n.*548G=
ENST00000643479.1:n.837G=
ENST00000643516.1:c.396-236G=
ENST00000644151.1:n.2247G=
ENST00000644218.1:c.808G= ENSP00000493574.1:p.Gly270=
ENST00000644683.1:c.*261G= ENSP00000494085.1:n.*261G=
ENST00000644810.1:c.529G= ENSP00000495895.1:p.Gly177=
ENST00000644831.1:n.984G=
ENST00000644933.1:c.79G= ENSP00000496133.1:p.Gly27=
ENST00000645020.1:n.2098G=
ENST00000645285.1:c.79G= ENSP00000495058.1:p.Gly27=
ENST00000645331.1:n.1174G=
ENST00000645620.1:c.79G= ENSP00000493657.1:p.Gly27=
ENST00000646777.1:n.984G=
ENST00000647016.1:n.1288G=
ENST00000647152.1:c.79G= ENSP00000495893.1:p.Gly27=
ENST00000647209.1:c.*677G= ENSP00000495558.1:n.*677G=
ENST00000647346.1:n.1828G=
ENST00000299427.10:c.808G= ENSP00000299427.6:p.Gly270=
ENST00000436873.6:c.451-236G= ENSP00000398136.2:n.451-236G=
ENST00000524788.1:n.508G=
ENST00000528807.1:n.358G=
ENST00000533371.5:c.79G= ENSP00000437066.1:p.Gly27=
ENST00000611494.4:c.808G= ENSP00000484546.1:p.Gly270=
NM_000391.3:c.808G= NP_000382.3:p.Gly270=
NM_000391.4:c.808G= MANE Select NP_000382.3:p.Gly270=