Canonical Allele Identifier: CA1950214832
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617318_6617352delinsGCCAAGGCCTGTGGAAGCTGGTAGGGATGTGGGGA , CM000673.2:g.6617318_6617352delinsGCCAAGGCCTGTGGAAGCTGGTAGGGATGTGGGGA GRCh38
NC_000011.9:g.6638549_6638583delinsGCCAAGGCCTGTGGAAGCTGGTAGGGATGTGGGGA , CM000673.1:g.6638549_6638583delinsGCCAAGGCCTGTGGAAGCTGGTAGGGATGTGGGGA GRCh37
NC_000011.8:g.6595125_6595159delinsGCCAAGGCCTGTGGAAGCTGGTAGGGATGTGGGGA NCBI36
NG_008653.1:g.7110_7144delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.343_377delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000507321.1:p.Ser115=
ENST00000299427.12:c.457_491delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC MANE Select ENSP00000299427.6:p.Ser153=
ENST00000428886.7:n.545_579delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000436873.7:c.261_295delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000524788.2:n.1469_1503delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000524903.2:n.1585_1619delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000528571.6:c.*197_*231delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000434647.1:n.*197_*231delinsTCCCCA...
ENST00000528807.2:n.113_147delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000530040.2:n.479+7_479+41delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000533371.6:c.-273_-239delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000437066.1:n.-273_-239delinsTCCCCA...
ENST00000534644.6:n.456+2_456+36delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000642892.1:c.-222+2_-222+36delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000494165.1:n.-222+2_-222+36delinsT...
ENST00000643439.1:c.*197_*231delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000495849.1:n.*197_*231delinsTCCCCA...
ENST00000643479.1:n.486_520delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000643516.1:c.344_378delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000644151.1:n.1749_1783delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000644218.1:c.457_491delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000493574.1:p.Ser153=
ENST00000644683.1:c.450+7_450+41delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000494085.1:n.450+7_450+41delinsTCC...
ENST00000644810.1:c.230-199_230-165delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000495895.1:n.230-199_230-165delins...
ENST00000644831.1:n.486_520delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000644933.1:c.-273_-239delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000496133.1:n.-273_-239delinsTCCCCA...
ENST00000645020.1:n.1485_1519delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000645285.1:c.-273_-239delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000495058.1:n.-273_-239delinsTCCCCA...
ENST00000645331.1:n.676_710delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000645620.1:c.-222+7_-222+41delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000493657.1:n.-222+7_-222+41delinsT...
ENST00000646777.1:n.486_520delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000647016.1:n.790_824delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000647152.1:c.-273_-239delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000495893.1:n.-273_-239delinsTCCCCA...
ENST00000647209.1:c.*326_*360delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000495558.1:n.*326_*360delinsTCCCCA...
ENST00000647346.1:n.1477_1511delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000299427.10:c.457_491delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000299427.6:p.Ser153=
ENST00000428886.6:n.479_513delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000436873.6:c.450+7_450+41delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000398136.2:n.450+7_450+41delinsTCC...
ENST00000524788.1:n.10_44delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000528571.5:c.*197_*231delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000434647.1:n.*197_*231delinsTCCCCA...
ENST00000533371.5:c.-273_-239delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000437066.1:n.-273_-239delinsTCCCCA...
ENST00000534644.5:n.442_476delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC
ENST00000611494.4:c.457_491delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC ENSP00000484546.1:p.Ser153=
NM_000391.3:c.457_491delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC NP_000382.3:p.Ser153=
NM_000391.4:c.457_491delinsTCCCCACATCCCTACCAGCTTCCACAGGCCTTGGC MANE Select NP_000382.3:p.Ser153=