Canonical Allele Identifier: CA2832564434

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615124dup , CM000673.2:g.6615124dup	GRCh38
NC_000011.9:g.6636355dup , CM000673.1:g.6636355dup	GRCh37
NC_000011.8:g.6592931dup	NCBI36
NG_008653.1:g.9342dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1311+51dup	ENSP00000507321.1:n.1311+51dup
ENST00000299427.12:c.1425+51dup MANE Select	ENSP00000299427.6:n.1425+51dup
ENST00000524611.2:n.285+51dup
ENST00000524924.2:n.545+51dup
ENST00000533371.6:c.696+51dup	ENSP00000437066.1:n.696+51dup
ENST00000642892.1:c.696+51dup	ENSP00000494165.1:n.696+51dup
ENST00000643342.1:c.498+51dup
ENST00000643439.1:c.*1165+51dup	ENSP00000495849.1:n.*1165+51dup
ENST00000643479.1:n.1611+51dup
ENST00000643516.1:c.934+51dup
ENST00000644218.1:c.1236+51dup	ENSP00000493574.1:n.1236+51dup
ENST00000644683.1:c.*878+51dup	ENSP00000494085.1:n.*878+51dup
ENST00000644810.1:c.1146+51dup	ENSP00000495895.1:n.1146+51dup
ENST00000644831.1:n.1601+51dup
ENST00000644933.1:c.*291+51dup	ENSP00000496133.1:n.*291+51dup
ENST00000645285.1:c.*291+51dup	ENSP00000495058.1:n.*291+51dup
ENST00000645331.1:n.2630+51dup
ENST00000645620.1:c.696+51dup	ENSP00000493657.1:n.696+51dup
ENST00000646691.1:n.1312+51dup
ENST00000646777.1:n.1758+51dup
ENST00000647016.1:n.1905+51dup
ENST00000647152.1:c.696+51dup	ENSP00000495893.1:n.696+51dup
ENST00000647209.1:c.*1294+51dup	ENSP00000495558.1:n.*1294+51dup
ENST00000647346.1:n.2445+51dup
ENST00000299427.10:c.1425+51dup	ENSP00000299427.6:n.1425+51dup
ENST00000524611.1:n.303+51dup
ENST00000533371.5:c.696+51dup	ENSP00000437066.1:n.696+51dup
ENST00000611494.4:c.1425+51dup	ENSP00000484546.1:n.1425+51dup
NM_000391.3:c.1425+51dup	NP_000382.3:n.1425+51dup
NM_000391.4:c.1425+51dup MANE Select	NP_000382.3:n.1425+51dup