Canonical Allele Identifier: CA1950237306
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616769C= , CM000673.2:g.6616769C= GRCh38
NC_000011.9:g.6638000C= , CM000673.1:g.6638000C= GRCh37
NC_000011.8:g.6594576C= NCBI36
NG_008653.1:g.7693G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.664G= ENSP00000507321.1:p.Val222=
ENST00000299427.12:c.778G= MANE Select ENSP00000299427.6:p.Val260=
ENST00000436873.7:c.312+532G=
ENST00000524788.2:n.1937G=
ENST00000524903.2:n.2053G=
ENST00000528807.2:n.434G=
ENST00000530040.2:n.480-266G=
ENST00000533371.6:c.49G= ENSP00000437066.1:p.Val17=
ENST00000642892.1:c.49G= ENSP00000494165.1:p.Val17=
ENST00000643439.1:c.*518G= ENSP00000495849.1:n.*518G=
ENST00000643479.1:n.807G=
ENST00000643516.1:c.396-266G=
ENST00000644151.1:n.2217G=
ENST00000644218.1:c.778G= ENSP00000493574.1:p.Val260=
ENST00000644683.1:c.*231G= ENSP00000494085.1:n.*231G=
ENST00000644810.1:c.499G= ENSP00000495895.1:p.Val167=
ENST00000644831.1:n.954G=
ENST00000644933.1:c.49G= ENSP00000496133.1:p.Val17=
ENST00000645020.1:n.2068G=
ENST00000645285.1:c.49G= ENSP00000495058.1:p.Val17=
ENST00000645331.1:n.1144G=
ENST00000645620.1:c.49G= ENSP00000493657.1:p.Val17=
ENST00000646777.1:n.954G=
ENST00000647016.1:n.1258G=
ENST00000647152.1:c.49G= ENSP00000495893.1:p.Val17=
ENST00000647209.1:c.*647G= ENSP00000495558.1:n.*647G=
ENST00000647346.1:n.1798G=
ENST00000299427.10:c.778G= ENSP00000299427.6:p.Val260=
ENST00000436873.6:c.451-266G= ENSP00000398136.2:n.451-266G=
ENST00000524788.1:n.478G=
ENST00000528807.1:n.328G=
ENST00000533371.5:c.49G= ENSP00000437066.1:p.Val17=
ENST00000611494.4:c.778G= ENSP00000484546.1:p.Val260=
NM_000391.3:c.778G= NP_000382.3:p.Val260=
NM_000391.4:c.778G= MANE Select NP_000382.3:p.Val260=