Canonical Allele Identifier: CA1950236924
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616528T= , CM000673.2:g.6616528T= GRCh38
NC_000011.9:g.6637759T= , CM000673.1:g.6637759T= GRCh37
NC_000011.8:g.6594335T= NCBI36
NG_008653.1:g.7934A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.773-25A= ENSP00000507321.1:n.773-25A=
ENST00000299427.12:c.887-25A= MANE Select ENSP00000299427.6:n.887-25A=
ENST00000436873.7:c.313-454A=
ENST00000524903.2:n.2294A=
ENST00000530040.2:n.480-25A=
ENST00000533371.6:c.158-25A= ENSP00000437066.1:n.158-25A=
ENST00000642892.1:c.158-25A= ENSP00000494165.1:n.158-25A=
ENST00000643439.1:c.*627-25A= ENSP00000495849.1:n.*627-25A=
ENST00000643479.1:n.1048A=
ENST00000643516.1:c.396-25A=
ENST00000644218.1:c.886+133A= ENSP00000493574.1:n.886+133A=
ENST00000644683.1:c.*340-25A= ENSP00000494085.1:n.*340-25A=
ENST00000644810.1:c.608-25A= ENSP00000495895.1:n.608-25A=
ENST00000644831.1:n.1063-25A=
ENST00000644933.1:c.158-25A= ENSP00000496133.1:n.158-25A=
ENST00000645285.1:c.157+133A= ENSP00000495058.1:n.157+133A=
ENST00000645331.1:n.1385A=
ENST00000645620.1:c.158-25A= ENSP00000493657.1:n.158-25A=
ENST00000646777.1:n.1195A=
ENST00000647016.1:n.1367-25A=
ENST00000647152.1:c.158-25A= ENSP00000495893.1:n.158-25A=
ENST00000647209.1:c.*756-25A= ENSP00000495558.1:n.*756-25A=
ENST00000647346.1:n.1907-25A=
ENST00000299427.10:c.887-25A= ENSP00000299427.6:n.887-25A=
ENST00000436873.6:c.451-25A= ENSP00000398136.2:n.451-25A=
ENST00000528807.1:n.569A=
ENST00000533371.5:c.158-25A= ENSP00000437066.1:n.158-25A=
ENST00000611494.4:c.887-25A= ENSP00000484546.1:n.887-25A=
NM_000391.3:c.887-25A= NP_000382.3:n.887-25A=
NM_000391.4:c.887-25A= MANE Select NP_000382.3:n.887-25A=