Canonical Allele Identifier: CA2612256251

Gene: TPP1

Linked Data

• gnomAD v4: 11-6617433-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617435del , CM000673.2:g.6617435del	GRCh38
NC_000011.9:g.6638666del , CM000673.1:g.6638666del	GRCh37
NC_000011.8:g.6595242del	NCBI36
NG_008653.1:g.7028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.267-6del	ENSP00000507321.1:n.267-6del
ENST00000299427.12:c.381-6del MANE Select	ENSP00000299427.6:n.381-6del
ENST00000428886.7:n.469-6del
ENST00000436873.7:c.185-6del
ENST00000524788.2:n.1393-6del
ENST00000524903.2:n.1509-6del
ENST00000528571.6:c.*121-6del	ENSP00000434647.1:n.*121-6del
ENST00000528807.2:n.31del
ENST00000530040.2:n.410-6del
ENST00000533371.6:c.-349-6del	ENSP00000437066.1:n.-349-6del
ENST00000534644.6:n.382-6del
ENST00000642892.1:c.-296-6del	ENSP00000494165.1:n.-296-6del
ENST00000643439.1:c.*121-6del	ENSP00000495849.1:n.*121-6del
ENST00000643479.1:n.410-6del
ENST00000643516.1:c.268-6del
ENST00000644151.1:n.1673-6del
ENST00000644218.1:c.381-6del	ENSP00000493574.1:n.381-6del
ENST00000644683.1:c.381-6del	ENSP00000494085.1:n.381-6del
ENST00000644810.1:c.230-281del	ENSP00000495895.1:n.230-281del
ENST00000644831.1:n.410-6del
ENST00000644933.1:c.-349-6del	ENSP00000496133.1:n.-349-6del
ENST00000645020.1:n.1409-6del
ENST00000645285.1:c.-349-6del	ENSP00000495058.1:n.-349-6del
ENST00000645331.1:n.594del
ENST00000645620.1:c.-291-6del	ENSP00000493657.1:n.-291-6del
ENST00000646777.1:n.410-6del
ENST00000647016.1:n.714-6del
ENST00000647152.1:c.-349-6del	ENSP00000495893.1:n.-349-6del
ENST00000647209.1:c.*250-6del	ENSP00000495558.1:n.*250-6del
ENST00000647346.1:n.1401-6del
ENST00000299427.10:c.381-6del	ENSP00000299427.6:n.381-6del
ENST00000428886.6:n.403-6del
ENST00000436873.6:c.381-6del	ENSP00000398136.2:n.381-6del
ENST00000528571.5:c.*121-6del	ENSP00000434647.1:n.*121-6del
ENST00000530040.1:n.493-6del
ENST00000533371.5:c.-349-6del	ENSP00000437066.1:n.-349-6del
ENST00000534644.5:n.366-6del
ENST00000611494.4:c.381-6del	ENSP00000484546.1:n.381-6del
NM_000391.3:c.381-6del	NP_000382.3:n.381-6del
NM_000391.4:c.381-6del MANE Select	NP_000382.3:n.381-6del