Canonical Allele Identifier: CA1950234397

Gene: TPP1

Linked Data

• dbSNP Id: rs1855564302

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615398dup , CM000673.2:g.6615398dup	GRCh38
NC_000011.9:g.6636629dup , CM000673.1:g.6636629dup	GRCh37
NC_000011.8:g.6593205dup	NCBI36
NG_008653.1:g.9068dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1152+48dup	ENSP00000507321.1:n.1152+48dup
ENST00000299427.12:c.1266+48dup MANE Select	ENSP00000299427.6:n.1266+48dup
ENST00000436873.7:c.503+48dup
ENST00000524611.2:n.62dup
ENST00000524924.2:n.386+48dup
ENST00000533371.6:c.537+48dup	ENSP00000437066.1:n.537+48dup
ENST00000642892.1:c.537+48dup	ENSP00000494165.1:n.537+48dup
ENST00000643342.1:c.339+48dup
ENST00000643439.1:c.*1006+48dup	ENSP00000495849.1:n.*1006+48dup
ENST00000643479.1:n.1452+48dup
ENST00000643516.1:c.775+48dup
ENST00000644218.1:c.1077+48dup	ENSP00000493574.1:n.1077+48dup
ENST00000644683.1:c.*719+48dup	ENSP00000494085.1:n.*719+48dup
ENST00000644810.1:c.987+48dup	ENSP00000495895.1:n.987+48dup
ENST00000644831.1:n.1442+48dup
ENST00000644933.1:c.*132+48dup	ENSP00000496133.1:n.*132+48dup
ENST00000645285.1:c.*132+48dup	ENSP00000495058.1:n.*132+48dup
ENST00000645331.1:n.2471+48dup
ENST00000645620.1:c.537+48dup	ENSP00000493657.1:n.537+48dup
ENST00000646691.1:n.1089dup
ENST00000646777.1:n.1599+48dup
ENST00000647016.1:n.1746+48dup
ENST00000647152.1:c.537+48dup	ENSP00000495893.1:n.537+48dup
ENST00000647209.1:c.*1135+48dup	ENSP00000495558.1:n.*1135+48dup
ENST00000647346.1:n.2286+48dup
ENST00000299427.10:c.1266+48dup	ENSP00000299427.6:n.1266+48dup
ENST00000524611.1:n.80dup
ENST00000524924.1:n.221+48dup
ENST00000532191.1:n.319+48dup
ENST00000533371.5:c.537+48dup	ENSP00000437066.1:n.537+48dup
ENST00000611494.4:c.1266+48dup	ENSP00000484546.1:n.1266+48dup
NM_000391.3:c.1266+48dup	NP_000382.3:n.1266+48dup
NM_000391.4:c.1266+48dup MANE Select	NP_000382.3:n.1266+48dup