Canonical Allele Identifier: CA1950237735
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616997T= , CM000673.2:g.6616997T= GRCh38
NC_000011.9:g.6638228T= , CM000673.1:g.6638228T= GRCh37
NC_000011.8:g.6594804T= NCBI36
NG_008653.1:g.7465A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.551A= ENSP00000507321.1:p.Asn184=
ENST00000299427.12:c.665A= MANE Select ENSP00000299427.6:p.Asn222=
ENST00000436873.7:c.312+304A=
ENST00000524788.2:n.1824A=
ENST00000524903.2:n.1940A=
ENST00000528807.2:n.321A=
ENST00000530040.2:n.479+362A=
ENST00000533371.6:c.-65A= ENSP00000437066.1:n.-65A=
ENST00000534644.6:n.613A=
ENST00000642892.1:c.-65A= ENSP00000494165.1:n.-65A=
ENST00000643439.1:c.*405A= ENSP00000495849.1:n.*405A=
ENST00000643479.1:n.694A=
ENST00000643516.1:c.395+304A=
ENST00000644151.1:n.2104A=
ENST00000644218.1:c.665A= ENSP00000493574.1:p.Asn222=
ENST00000644683.1:c.*118A= ENSP00000494085.1:n.*118A=
ENST00000644810.1:c.386A= ENSP00000495895.1:p.Asn129=
ENST00000644831.1:n.841A=
ENST00000644933.1:c.-65A= ENSP00000496133.1:n.-65A=
ENST00000645020.1:n.1840A=
ENST00000645285.1:c.-65A= ENSP00000495058.1:n.-65A=
ENST00000645331.1:n.1031A=
ENST00000645620.1:c.-65A= ENSP00000493657.1:n.-65A=
ENST00000646777.1:n.841A=
ENST00000647016.1:n.1145A=
ENST00000647152.1:c.-65A= ENSP00000495893.1:n.-65A=
ENST00000647209.1:c.*534A= ENSP00000495558.1:n.*534A=
ENST00000647346.1:n.1685A=
ENST00000299427.10:c.665A= ENSP00000299427.6:p.Asn222=
ENST00000428886.6:n.834A=
ENST00000436873.6:c.450+362A= ENSP00000398136.2:n.450+362A=
ENST00000524788.1:n.365A=
ENST00000528571.5:c.*405A= ENSP00000434647.1:n.*405A=
ENST00000528807.1:n.215A=
ENST00000533371.5:c.-65A= ENSP00000437066.1:n.-65A=
ENST00000611494.4:c.665A= ENSP00000484546.1:p.Asn222=
NM_000391.3:c.665A= NP_000382.3:p.Asn222=
NM_000391.4:c.665A= MANE Select NP_000382.3:p.Asn222=