Canonical Allele Identifier: CA2612258507

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616900-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616900G>T , CM000673.2:g.6616900G>T	GRCh38
NC_000011.9:g.6638131G>T , CM000673.1:g.6638131G>T	GRCh37
NC_000011.8:g.6594707G>T	NCBI36
NG_008653.1:g.7562C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.574-41C>A	ENSP00000507321.1:n.574-41C>A
ENST00000299427.12:c.688-41C>A MANE Select	ENSP00000299427.6:n.688-41C>A
ENST00000436873.7:c.312+401C>A
ENST00000524788.2:n.1847-41C>A
ENST00000524903.2:n.1963-41C>A
ENST00000528807.2:n.344-41C>A
ENST00000530040.2:n.480-397C>A
ENST00000533371.6:c.-42-41C>A	ENSP00000437066.1:n.-42-41C>A
ENST00000642892.1:c.-42-41C>A	ENSP00000494165.1:n.-42-41C>A
ENST00000643439.1:c.*428-41C>A	ENSP00000495849.1:n.*428-41C>A
ENST00000643479.1:n.717-41C>A
ENST00000643516.1:c.396-397C>A
ENST00000644151.1:n.2127-41C>A
ENST00000644218.1:c.688-41C>A	ENSP00000493574.1:n.688-41C>A
ENST00000644683.1:c.*141-41C>A	ENSP00000494085.1:n.*141-41C>A
ENST00000644810.1:c.409-41C>A	ENSP00000495895.1:n.409-41C>A
ENST00000644831.1:n.864-41C>A
ENST00000644933.1:c.-42-41C>A	ENSP00000496133.1:n.-42-41C>A
ENST00000645020.1:n.1937C>A
ENST00000645285.1:c.-42-41C>A	ENSP00000495058.1:n.-42-41C>A
ENST00000645331.1:n.1054-41C>A
ENST00000645620.1:c.-42-41C>A	ENSP00000493657.1:n.-42-41C>A
ENST00000646777.1:n.864-41C>A
ENST00000647016.1:n.1168-41C>A
ENST00000647152.1:c.-42-41C>A	ENSP00000495893.1:n.-42-41C>A
ENST00000647209.1:c.*557-41C>A	ENSP00000495558.1:n.*557-41C>A
ENST00000647346.1:n.1708-41C>A
ENST00000299427.10:c.688-41C>A	ENSP00000299427.6:n.688-41C>A
ENST00000436873.6:c.451-397C>A	ENSP00000398136.2:n.451-397C>A
ENST00000524788.1:n.388-41C>A
ENST00000528807.1:n.238-41C>A
ENST00000533371.5:c.-42-41C>A	ENSP00000437066.1:n.-42-41C>A
ENST00000611494.4:c.688-41C>A	ENSP00000484546.1:n.688-41C>A
NM_000391.3:c.688-41C>A	NP_000382.3:n.688-41C>A
NM_000391.4:c.688-41C>A MANE Select	NP_000382.3:n.688-41C>A