Canonical Allele Identifier: CA1950237047
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616618A= , CM000673.2:g.6616618A= GRCh38
NC_000011.9:g.6637849A= , CM000673.1:g.6637849A= GRCh37
NC_000011.8:g.6594425A= NCBI36
NG_008653.1:g.7844T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.772+43T= ENSP00000507321.1:n.772+43T=
ENST00000299427.12:c.886+43T= MANE Select ENSP00000299427.6:n.886+43T=
ENST00000436873.7:c.313-544T=
ENST00000524788.2:n.2088T=
ENST00000524903.2:n.2204T=
ENST00000528807.2:n.585T=
ENST00000530040.2:n.480-115T=
ENST00000533371.6:c.157+43T= ENSP00000437066.1:n.157+43T=
ENST00000642892.1:c.157+43T= ENSP00000494165.1:n.157+43T=
ENST00000643439.1:c.*626+43T= ENSP00000495849.1:n.*626+43T=
ENST00000643479.1:n.958T=
ENST00000643516.1:c.396-115T=
ENST00000644218.1:c.886+43T= ENSP00000493574.1:n.886+43T=
ENST00000644683.1:c.*339+43T= ENSP00000494085.1:n.*339+43T=
ENST00000644810.1:c.607+43T= ENSP00000495895.1:n.607+43T=
ENST00000644831.1:n.1062+43T=
ENST00000644933.1:c.157+43T= ENSP00000496133.1:n.157+43T=
ENST00000645020.1:n.2219T=
ENST00000645285.1:c.157+43T= ENSP00000495058.1:n.157+43T=
ENST00000645331.1:n.1295T=
ENST00000645620.1:c.157+43T= ENSP00000493657.1:n.157+43T=
ENST00000646777.1:n.1105T=
ENST00000647016.1:n.1366+43T=
ENST00000647152.1:c.157+43T= ENSP00000495893.1:n.157+43T=
ENST00000647209.1:c.*755+43T= ENSP00000495558.1:n.*755+43T=
ENST00000647346.1:n.1906+43T=
ENST00000299427.10:c.886+43T= ENSP00000299427.6:n.886+43T=
ENST00000436873.6:c.451-115T= ENSP00000398136.2:n.451-115T=
ENST00000528807.1:n.479T=
ENST00000533371.5:c.157+43T= ENSP00000437066.1:n.157+43T=
ENST00000611494.4:c.886+43T= ENSP00000484546.1:n.886+43T=
NM_000391.3:c.886+43T= NP_000382.3:n.886+43T=
NM_000391.4:c.886+43T= MANE Select NP_000382.3:n.886+43T=