Canonical Allele Identifier: CA2612257972

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616173-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616174del , CM000673.2:g.6616174del	GRCh38
NC_000011.9:g.6637405del , CM000673.1:g.6637405del	GRCh37
NC_000011.8:g.6593981del	NCBI36
NG_008653.1:g.8288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.962-100del	ENSP00000507321.1:n.962-100del
ENST00000299427.12:c.1076-100del MANE Select	ENSP00000299427.6:n.1076-100del
ENST00000436873.7:c.313-100del
ENST00000524924.2:n.96del
ENST00000533371.6:c.347-100del	ENSP00000437066.1:n.347-100del
ENST00000642892.1:c.347-100del	ENSP00000494165.1:n.347-100del
ENST00000643342.1:c.166-100del
ENST00000643439.1:c.*816-100del	ENSP00000495849.1:n.*816-100del
ENST00000643479.1:n.1262-100del
ENST00000643516.1:c.585-100del
ENST00000644218.1:c.887-100del	ENSP00000493574.1:n.887-100del
ENST00000644683.1:c.*529-100del	ENSP00000494085.1:n.*529-100del
ENST00000644810.1:c.797-100del	ENSP00000495895.1:n.797-100del
ENST00000644831.1:n.1252-100del
ENST00000644933.1:c.347-100del	ENSP00000496133.1:n.347-100del
ENST00000645285.1:c.158-100del	ENSP00000495058.1:n.158-100del
ENST00000645331.1:n.1739del
ENST00000645620.1:c.347-100del	ENSP00000493657.1:n.347-100del
ENST00000646691.1:n.309del
ENST00000646777.1:n.1409-100del
ENST00000647016.1:n.1556-100del
ENST00000647152.1:c.347-100del	ENSP00000495893.1:n.347-100del
ENST00000647209.1:c.*945-100del	ENSP00000495558.1:n.*945-100del
ENST00000647346.1:n.2096-100del
ENST00000299427.10:c.1076-100del	ENSP00000299427.6:n.1076-100del
ENST00000533371.5:c.347-100del	ENSP00000437066.1:n.347-100del
ENST00000611494.4:c.1076-100del	ENSP00000484546.1:n.1076-100del
NM_000391.3:c.1076-100del	NP_000382.3:n.1076-100del
NM_000391.4:c.1076-100del MANE Select	NP_000382.3:n.1076-100del