Canonical Allele Identifier: CA1950238358
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617267G= , CM000673.2:g.6617267G= GRCh38
NC_000011.9:g.6638498G= , CM000673.1:g.6638498G= GRCh37
NC_000011.8:g.6595074G= NCBI36
NG_008653.1:g.7195C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.394+34C= ENSP00000507321.1:n.394+34C=
ENST00000299427.12:c.508+34C= MANE Select ENSP00000299427.6:n.508+34C=
ENST00000428886.7:n.630C=
ENST00000436873.7:c.312+34C=
ENST00000524788.2:n.1554C=
ENST00000524903.2:n.1670C=
ENST00000528571.6:c.*282C= ENSP00000434647.1:n.*282C=
ENST00000528807.2:n.164+34C=
ENST00000530040.2:n.479+92C=
ENST00000533371.6:c.-222+34C= ENSP00000437066.1:n.-222+34C=
ENST00000534644.6:n.456+87C=
ENST00000642892.1:c.-222+87C= ENSP00000494165.1:n.-222+87C=
ENST00000643439.1:c.*248+34C= ENSP00000495849.1:n.*248+34C=
ENST00000643479.1:n.537+34C=
ENST00000643516.1:c.395+34C=
ENST00000644151.1:n.1834C=
ENST00000644218.1:c.508+34C= ENSP00000493574.1:n.508+34C=
ENST00000644683.1:c.450+92C= ENSP00000494085.1:n.450+92C=
ENST00000644810.1:c.230-114C= ENSP00000495895.1:n.230-114C=
ENST00000644831.1:n.571C=
ENST00000644933.1:c.-222+34C= ENSP00000496133.1:n.-222+34C=
ENST00000645020.1:n.1570C=
ENST00000645285.1:c.-222+34C= ENSP00000495058.1:n.-222+34C=
ENST00000645331.1:n.761C=
ENST00000645620.1:c.-222+92C= ENSP00000493657.1:n.-222+92C=
ENST00000646777.1:n.571C=
ENST00000647016.1:n.875C=
ENST00000647152.1:c.-222+34C= ENSP00000495893.1:n.-222+34C=
ENST00000647209.1:c.*377+34C= ENSP00000495558.1:n.*377+34C=
ENST00000647346.1:n.1528+34C=
ENST00000299427.10:c.508+34C= ENSP00000299427.6:n.508+34C=
ENST00000428886.6:n.564C=
ENST00000436873.6:c.450+92C= ENSP00000398136.2:n.450+92C=
ENST00000524788.1:n.95C=
ENST00000528571.5:c.*248+34C= ENSP00000434647.1:n.*248+34C=
ENST00000533371.5:c.-222+34C= ENSP00000437066.1:n.-222+34C=
ENST00000534644.5:n.493+34C=
ENST00000611494.4:c.508+34C= ENSP00000484546.1:n.508+34C=
NM_000391.3:c.508+34C= NP_000382.3:n.508+34C=
NM_000391.4:c.508+34C= MANE Select NP_000382.3:n.508+34C=