Canonical Allele Identifier: CA1950214867
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617338G= , CM000673.2:g.6617338G= GRCh38
NC_000011.9:g.6638569G= , CM000673.1:g.6638569G= GRCh37
NC_000011.8:g.6595145G= NCBI36
NG_008653.1:g.7124C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.357C= ENSP00000507321.1:p.Tyr119=
ENST00000299427.12:c.471C= MANE Select ENSP00000299427.6:p.Tyr157=
ENST00000428886.7:n.559C=
ENST00000436873.7:c.275C=
ENST00000524788.2:n.1483C=
ENST00000524903.2:n.1599C=
ENST00000528571.6:c.*211C= ENSP00000434647.1:n.*211C=
ENST00000528807.2:n.127C=
ENST00000530040.2:n.479+21C=
ENST00000533371.6:c.-259C= ENSP00000437066.1:n.-259C=
ENST00000534644.6:n.456+16C=
ENST00000642892.1:c.-222+16C= ENSP00000494165.1:n.-222+16C=
ENST00000643439.1:c.*211C= ENSP00000495849.1:n.*211C=
ENST00000643479.1:n.500C=
ENST00000643516.1:c.358C=
ENST00000644151.1:n.1763C=
ENST00000644218.1:c.471C= ENSP00000493574.1:p.Tyr157=
ENST00000644683.1:c.450+21C= ENSP00000494085.1:n.450+21C=
ENST00000644810.1:c.230-185C= ENSP00000495895.1:n.230-185C=
ENST00000644831.1:n.500C=
ENST00000644933.1:c.-259C= ENSP00000496133.1:n.-259C=
ENST00000645020.1:n.1499C=
ENST00000645285.1:c.-259C= ENSP00000495058.1:n.-259C=
ENST00000645331.1:n.690C=
ENST00000645620.1:c.-222+21C= ENSP00000493657.1:n.-222+21C=
ENST00000646777.1:n.500C=
ENST00000647016.1:n.804C=
ENST00000647152.1:c.-259C= ENSP00000495893.1:n.-259C=
ENST00000647209.1:c.*340C= ENSP00000495558.1:n.*340C=
ENST00000647346.1:n.1491C=
ENST00000299427.10:c.471C= ENSP00000299427.6:p.Tyr157=
ENST00000428886.6:n.493C=
ENST00000436873.6:c.450+21C= ENSP00000398136.2:n.450+21C=
ENST00000524788.1:n.24C=
ENST00000528571.5:c.*211C= ENSP00000434647.1:n.*211C=
ENST00000533371.5:c.-259C= ENSP00000437066.1:n.-259C=
ENST00000534644.5:n.456C=
ENST00000611494.4:c.471C= ENSP00000484546.1:p.Tyr157=
NM_000391.3:c.471C= NP_000382.3:p.Tyr157=
NM_000391.4:c.471C= MANE Select NP_000382.3:p.Tyr157=