Canonical Allele Identifier: CA1950232835

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614689_6614690delinsAG , CM000673.2:g.6614689_6614690delinsAG	GRCh38
NC_000011.9:g.6635920_6635921delinsAG , CM000673.1:g.6635920_6635921delinsAG	GRCh37
NC_000011.8:g.6592496_6592497delinsAG	NCBI36
NG_008653.1:g.9772_9773delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1438-4_1438-3delinsCT	ENSP00000507321.1:n.1438-4_1438-3delinsCT
ENST00000299427.12:c.1552-4_1552-3delinsCT MANE Select	ENSP00000299427.6:n.1552-4_1552-3delinsCT
ENST00000524611.2:n.587_588delinsCT
ENST00000524924.2:n.672-4_672-3delinsCT
ENST00000533371.6:c.823-4_823-3delinsCT	ENSP00000437066.1:n.823-4_823-3delinsCT
ENST00000642892.1:c.823-4_823-3delinsCT	ENSP00000494165.1:n.823-4_823-3delinsCT
ENST00000643342.1:c.625-4_625-3delinsCT
ENST00000643439.1:c.*1292-4_*1292-3delinsCT	ENSP00000495849.1:n.*1292-4_*1292-3delinsCT
ENST00000643479.1:n.1738-4_1738-3delinsCT
ENST00000643516.1:c.1061-4_1061-3delinsCT
ENST00000644218.1:c.1363-4_1363-3delinsCT	ENSP00000493574.1:n.1363-4_1363-3delinsCT
ENST00000644683.1:c.*1005-4_*1005-3delinsCT	ENSP00000494085.1:n.*1005-4_*1005-3delinsCT
ENST00000644810.1:c.1273-4_1273-3delinsCT	ENSP00000495895.1:n.1273-4_1273-3delinsCT
ENST00000644831.1:n.1728-4_1728-3delinsCT
ENST00000644933.1:c.*418-4_*418-3delinsCT	ENSP00000496133.1:n.*418-4_*418-3delinsCT
ENST00000645285.1:c.*418-4_*418-3delinsCT	ENSP00000495058.1:n.*418-4_*418-3delinsCT
ENST00000645331.1:n.2757-4_2757-3delinsCT
ENST00000645620.1:c.823-4_823-3delinsCT	ENSP00000493657.1:n.823-4_823-3delinsCT
ENST00000646691.1:n.1439-4_1439-3delinsCT
ENST00000646777.1:n.1885-4_1885-3delinsCT
ENST00000647016.1:n.2032-4_2032-3delinsCT
ENST00000647152.1:c.823-4_823-3delinsCT	ENSP00000495893.1:n.823-4_823-3delinsCT
ENST00000647209.1:c.*1421-4_*1421-3delinsCT	ENSP00000495558.1:n.*1421-4_*1421-3delinsCT
ENST00000647346.1:n.2572-4_2572-3delinsCT
ENST00000299427.10:c.1552-4_1552-3delinsCT	ENSP00000299427.6:n.1552-4_1552-3delinsCT
ENST00000524611.1:n.430-4_430-3delinsCT
ENST00000533371.5:c.823-4_823-3delinsCT	ENSP00000437066.1:n.823-4_823-3delinsCT
ENST00000611494.4:c.1552-4_1552-3delinsCT	ENSP00000484546.1:n.1552-4_1552-3delinsCT
NM_000391.3:c.1552-4_1552-3delinsCT	NP_000382.3:n.1552-4_1552-3delinsCT
NM_000391.4:c.1552-4_1552-3delinsCT MANE Select	NP_000382.3:n.1552-4_1552-3delinsCT