Canonical Allele Identifier: CA1950234122
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6615276A= , CM000673.2:g.6615276A= GRCh38
NC_000011.9:g.6636507A= , CM000673.1:g.6636507A= GRCh37
NC_000011.8:g.6593083A= NCBI36
NG_008653.1:g.9186T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.1206T= ENSP00000507321.1:p.Ser402=
ENST00000299427.12:c.1320T= MANE Select ENSP00000299427.6:p.Ser440=
ENST00000524611.2:n.180T=
ENST00000524924.2:n.440T=
ENST00000533371.6:c.591T= ENSP00000437066.1:p.Ser197=
ENST00000642892.1:c.591T= ENSP00000494165.1:p.Ser197=
ENST00000643342.1:c.393T=
ENST00000643439.1:c.*1060T= ENSP00000495849.1:n.*1060T=
ENST00000643479.1:n.1506T=
ENST00000643516.1:c.829T=
ENST00000644218.1:c.1131T= ENSP00000493574.1:p.Ser377=
ENST00000644683.1:c.*773T= ENSP00000494085.1:n.*773T=
ENST00000644810.1:c.1041T= ENSP00000495895.1:p.Ser347=
ENST00000644831.1:n.1496T=
ENST00000644933.1:c.*186T= ENSP00000496133.1:n.*186T=
ENST00000645285.1:c.*186T= ENSP00000495058.1:n.*186T=
ENST00000645331.1:n.2525T=
ENST00000645620.1:c.591T= ENSP00000493657.1:p.Ser197=
ENST00000646691.1:n.1207T=
ENST00000646777.1:n.1653T=
ENST00000647016.1:n.1800T=
ENST00000647152.1:c.591T= ENSP00000495893.1:p.Ser197=
ENST00000647209.1:c.*1189T= ENSP00000495558.1:n.*1189T=
ENST00000647346.1:n.2340T=
ENST00000299427.10:c.1320T= ENSP00000299427.6:p.Ser440=
ENST00000524611.1:n.198T=
ENST00000524924.1:n.275T=
ENST00000532191.1:n.373T=
ENST00000533371.5:c.591T= ENSP00000437066.1:p.Ser197=
ENST00000611494.4:c.1320T= ENSP00000484546.1:p.Ser440=
NM_000391.3:c.1320T= NP_000382.3:p.Ser440=
NM_000391.4:c.1320T= MANE Select NP_000382.3:p.Ser440=