Canonical Allele Identifier: CA1950214896
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617360A= , CM000673.2:g.6617360A= GRCh38
NC_000011.9:g.6638591A= , CM000673.1:g.6638591A= GRCh37
NC_000011.8:g.6595167A= NCBI36
NG_008653.1:g.7102T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.335T= ENSP00000507321.1:p.Val112=
ENST00000299427.12:c.449T= MANE Select ENSP00000299427.6:p.Val150=
ENST00000428886.7:n.537T=
ENST00000436873.7:c.253T=
ENST00000524788.2:n.1461T=
ENST00000524903.2:n.1577T=
ENST00000528571.6:c.*189T= ENSP00000434647.1:n.*189T=
ENST00000528807.2:n.105T=
ENST00000530040.2:n.478T=
ENST00000533371.6:c.-281T= ENSP00000437066.1:n.-281T=
ENST00000534644.6:n.450T=
ENST00000642892.1:c.-228T= ENSP00000494165.1:n.-228T=
ENST00000643439.1:c.*189T= ENSP00000495849.1:n.*189T=
ENST00000643479.1:n.478T=
ENST00000643516.1:c.336T=
ENST00000644151.1:n.1741T=
ENST00000644218.1:c.449T= ENSP00000493574.1:p.Val150=
ENST00000644683.1:c.449T= ENSP00000494085.1:p.Val150=
ENST00000644810.1:c.230-207T= ENSP00000495895.1:n.230-207T=
ENST00000644831.1:n.478T=
ENST00000644933.1:c.-281T= ENSP00000496133.1:n.-281T=
ENST00000645020.1:n.1477T=
ENST00000645285.1:c.-281T= ENSP00000495058.1:n.-281T=
ENST00000645331.1:n.668T=
ENST00000645620.1:c.-223T= ENSP00000493657.1:n.-223T=
ENST00000646777.1:n.478T=
ENST00000647016.1:n.782T=
ENST00000647152.1:c.-281T= ENSP00000495893.1:n.-281T=
ENST00000647209.1:c.*318T= ENSP00000495558.1:n.*318T=
ENST00000647346.1:n.1469T=
ENST00000299427.10:c.449T= ENSP00000299427.6:p.Val150=
ENST00000428886.6:n.471T=
ENST00000436873.6:c.449T= ENSP00000398136.2:p.Val150=
ENST00000524788.1:n.2T=
ENST00000528571.5:c.*189T= ENSP00000434647.1:n.*189T=
ENST00000533371.5:c.-281T= ENSP00000437066.1:n.-281T=
ENST00000534644.5:n.434T=
ENST00000611494.4:c.449T= ENSP00000484546.1:p.Val150=
NM_000391.3:c.449T= NP_000382.3:p.Val150=
NM_000391.4:c.449T= MANE Select NP_000382.3:p.Val150=