Canonical Allele Identifier: CA2612256792

Gene: TPP1

Linked Data

• gnomAD v4: 11-6615069-AGACAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615070_6615074del , CM000673.2:g.6615070_6615074del	GRCh38
NC_000011.9:g.6636301_6636305del , CM000673.1:g.6636301_6636305del	GRCh37
NC_000011.8:g.6592877_6592881del	NCBI36
NG_008653.1:g.9388_9392del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1312-83_1312-79del	ENSP00000507321.1:n.1312-83_1312-79del
ENST00000299427.12:c.1426-83_1426-79del MANE Select	ENSP00000299427.6:n.1426-83_1426-79del
ENST00000524611.2:n.286-83_286-79del
ENST00000524924.2:n.546-83_546-79del
ENST00000533371.6:c.697-83_697-79del	ENSP00000437066.1:n.697-83_697-79del
ENST00000642892.1:c.697-83_697-79del	ENSP00000494165.1:n.697-83_697-79del
ENST00000643342.1:c.499-83_499-79del
ENST00000643439.1:c.*1166-83_*1166-79del	ENSP00000495849.1:n.*1166-83_*1166-79del
ENST00000643479.1:n.1612-83_1612-79del
ENST00000643516.1:c.935-83_935-79del
ENST00000644218.1:c.1237-83_1237-79del	ENSP00000493574.1:n.1237-83_1237-79del
ENST00000644683.1:c.*879-83_*879-79del	ENSP00000494085.1:n.*879-83_*879-79del
ENST00000644810.1:c.1147-83_1147-79del	ENSP00000495895.1:n.1147-83_1147-79del
ENST00000644831.1:n.1602-83_1602-79del
ENST00000644933.1:c.*292-83_*292-79del	ENSP00000496133.1:n.*292-83_*292-79del
ENST00000645285.1:c.*292-83_*292-79del	ENSP00000495058.1:n.*292-83_*292-79del
ENST00000645331.1:n.2631-83_2631-79del
ENST00000645620.1:c.697-83_697-79del	ENSP00000493657.1:n.697-83_697-79del
ENST00000646691.1:n.1313-83_1313-79del
ENST00000646777.1:n.1759-83_1759-79del
ENST00000647016.1:n.1906-83_1906-79del
ENST00000647152.1:c.697-83_697-79del	ENSP00000495893.1:n.697-83_697-79del
ENST00000647209.1:c.*1295-83_*1295-79del	ENSP00000495558.1:n.*1295-83_*1295-79del
ENST00000647346.1:n.2446-83_2446-79del
ENST00000299427.10:c.1426-83_1426-79del	ENSP00000299427.6:n.1426-83_1426-79del
ENST00000524611.1:n.304-83_304-79del
ENST00000533371.5:c.697-83_697-79del	ENSP00000437066.1:n.697-83_697-79del
ENST00000611494.4:c.1426-83_1426-79del	ENSP00000484546.1:n.1426-83_1426-79del
NM_000391.3:c.1426-83_1426-79del	NP_000382.3:n.1426-83_1426-79del
NM_000391.4:c.1426-83_1426-79del MANE Select	NP_000382.3:n.1426-83_1426-79del