Canonical Allele Identifier: CA2612258003

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616247-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616247C>G , CM000673.2:g.6616247C>G	GRCh38
NC_000011.9:g.6637478C>G , CM000673.1:g.6637478C>G	GRCh37
NC_000011.8:g.6594054C>G	NCBI36
NG_008653.1:g.8215G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.961+68G>C	ENSP00000507321.1:n.961+68G>C
ENST00000299427.12:c.1075+68G>C MANE Select	ENSP00000299427.6:n.1075+68G>C
ENST00000436873.7:c.313-173G>C
ENST00000524924.2:n.23G>C
ENST00000533371.6:c.346+68G>C	ENSP00000437066.1:n.346+68G>C
ENST00000642892.1:c.346+68G>C	ENSP00000494165.1:n.346+68G>C
ENST00000643342.1:c.165+68G>C
ENST00000643439.1:c.*815+68G>C	ENSP00000495849.1:n.*815+68G>C
ENST00000643479.1:n.1261+68G>C
ENST00000643516.1:c.584+68G>C
ENST00000644218.1:c.887-173G>C	ENSP00000493574.1:n.887-173G>C
ENST00000644683.1:c.*528+68G>C	ENSP00000494085.1:n.*528+68G>C
ENST00000644810.1:c.796+68G>C	ENSP00000495895.1:n.796+68G>C
ENST00000644831.1:n.1251+68G>C
ENST00000644933.1:c.346+68G>C	ENSP00000496133.1:n.346+68G>C
ENST00000645285.1:c.158-173G>C	ENSP00000495058.1:n.158-173G>C
ENST00000645331.1:n.1666G>C
ENST00000645620.1:c.346+68G>C	ENSP00000493657.1:n.346+68G>C
ENST00000646691.1:n.236G>C
ENST00000646777.1:n.1408+68G>C
ENST00000647016.1:n.1555+68G>C
ENST00000647152.1:c.346+68G>C	ENSP00000495893.1:n.346+68G>C
ENST00000647209.1:c.*944+68G>C	ENSP00000495558.1:n.*944+68G>C
ENST00000647346.1:n.2095+68G>C
ENST00000299427.10:c.1075+68G>C	ENSP00000299427.6:n.1075+68G>C
ENST00000533371.5:c.346+68G>C	ENSP00000437066.1:n.346+68G>C
ENST00000611494.4:c.1075+68G>C	ENSP00000484546.1:n.1075+68G>C
NM_000391.3:c.1075+68G>C	NP_000382.3:n.1075+68G>C
NM_000391.4:c.1075+68G>C MANE Select	NP_000382.3:n.1075+68G>C