Canonical Allele Identifier: CA2832564436

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616630dup , CM000673.2:g.6616630dup	GRCh38
NC_000011.9:g.6637861dup , CM000673.1:g.6637861dup	GRCh37
NC_000011.8:g.6594437dup	NCBI36
NG_008653.1:g.7836dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.772+35dup	ENSP00000507321.1:n.772+35dup
ENST00000299427.12:c.886+35dup MANE Select	ENSP00000299427.6:n.886+35dup
ENST00000436873.7:c.313-552dup
ENST00000524788.2:n.2080dup
ENST00000524903.2:n.2196dup
ENST00000528807.2:n.577dup
ENST00000530040.2:n.480-123dup
ENST00000533371.6:c.157+35dup	ENSP00000437066.1:n.157+35dup
ENST00000642892.1:c.157+35dup	ENSP00000494165.1:n.157+35dup
ENST00000643439.1:c.*626+35dup	ENSP00000495849.1:n.*626+35dup
ENST00000643479.1:n.950dup
ENST00000643516.1:c.396-123dup
ENST00000644218.1:c.886+35dup	ENSP00000493574.1:n.886+35dup
ENST00000644683.1:c.*339+35dup	ENSP00000494085.1:n.*339+35dup
ENST00000644810.1:c.607+35dup	ENSP00000495895.1:n.607+35dup
ENST00000644831.1:n.1062+35dup
ENST00000644933.1:c.157+35dup	ENSP00000496133.1:n.157+35dup
ENST00000645020.1:n.2211dup
ENST00000645285.1:c.157+35dup	ENSP00000495058.1:n.157+35dup
ENST00000645331.1:n.1287dup
ENST00000645620.1:c.157+35dup	ENSP00000493657.1:n.157+35dup
ENST00000646777.1:n.1097dup
ENST00000647016.1:n.1366+35dup
ENST00000647152.1:c.157+35dup	ENSP00000495893.1:n.157+35dup
ENST00000647209.1:c.*755+35dup	ENSP00000495558.1:n.*755+35dup
ENST00000647346.1:n.1906+35dup
ENST00000299427.10:c.886+35dup	ENSP00000299427.6:n.886+35dup
ENST00000436873.6:c.451-123dup	ENSP00000398136.2:n.451-123dup
ENST00000528807.1:n.471dup
ENST00000533371.5:c.157+35dup	ENSP00000437066.1:n.157+35dup
ENST00000611494.4:c.886+35dup	ENSP00000484546.1:n.886+35dup
NM_000391.3:c.886+35dup	NP_000382.3:n.886+35dup
NM_000391.4:c.886+35dup MANE Select	NP_000382.3:n.886+35dup