Canonical Allele Identifier: CA1950232892

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614725_6614726delinsAC , CM000673.2:g.6614725_6614726delinsAC	GRCh38
NC_000011.9:g.6635956_6635957delinsAC , CM000673.1:g.6635956_6635957delinsAC	GRCh37
NC_000011.8:g.6592532_6592533delinsAC	NCBI36
NG_008653.1:g.9736_9737delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1438-40_1438-39delinsGT	ENSP00000507321.1:n.1438-40_1438-39delinsGT
ENST00000299427.12:c.1552-40_1552-39delinsGT MANE Select	ENSP00000299427.6:n.1552-40_1552-39delinsGT
ENST00000524611.2:n.551_552delinsGT
ENST00000524924.2:n.672-40_672-39delinsGT
ENST00000533371.6:c.823-40_823-39delinsGT	ENSP00000437066.1:n.823-40_823-39delinsGT
ENST00000642892.1:c.823-40_823-39delinsGT	ENSP00000494165.1:n.823-40_823-39delinsGT
ENST00000643342.1:c.625-40_625-39delinsGT
ENST00000643439.1:c.*1292-40_*1292-39delinsGT	ENSP00000495849.1:n.*1292-40_*1292-39delinsGT
ENST00000643479.1:n.1738-40_1738-39delinsGT
ENST00000643516.1:c.1061-40_1061-39delinsGT
ENST00000644218.1:c.1363-40_1363-39delinsGT	ENSP00000493574.1:n.1363-40_1363-39delinsGT
ENST00000644683.1:c.*1005-40_*1005-39delinsGT	ENSP00000494085.1:n.*1005-40_*1005-39delinsGT
ENST00000644810.1:c.1273-40_1273-39delinsGT	ENSP00000495895.1:n.1273-40_1273-39delinsGT
ENST00000644831.1:n.1728-40_1728-39delinsGT
ENST00000644933.1:c.*418-40_*418-39delinsGT	ENSP00000496133.1:n.*418-40_*418-39delinsGT
ENST00000645285.1:c.*418-40_*418-39delinsGT	ENSP00000495058.1:n.*418-40_*418-39delinsGT
ENST00000645331.1:n.2757-40_2757-39delinsGT
ENST00000645620.1:c.823-40_823-39delinsGT	ENSP00000493657.1:n.823-40_823-39delinsGT
ENST00000646691.1:n.1439-40_1439-39delinsGT
ENST00000646777.1:n.1885-40_1885-39delinsGT
ENST00000647016.1:n.2032-40_2032-39delinsGT
ENST00000647152.1:c.823-40_823-39delinsGT	ENSP00000495893.1:n.823-40_823-39delinsGT
ENST00000647209.1:c.*1421-40_*1421-39delinsGT	ENSP00000495558.1:n.*1421-40_*1421-39delinsGT
ENST00000647346.1:n.2572-40_2572-39delinsGT
ENST00000299427.10:c.1552-40_1552-39delinsGT	ENSP00000299427.6:n.1552-40_1552-39delinsGT
ENST00000524611.1:n.430-40_430-39delinsGT
ENST00000533371.5:c.823-40_823-39delinsGT	ENSP00000437066.1:n.823-40_823-39delinsGT
ENST00000611494.4:c.1552-40_1552-39delinsGT	ENSP00000484546.1:n.1552-40_1552-39delinsGT
NM_000391.3:c.1552-40_1552-39delinsGT	NP_000382.3:n.1552-40_1552-39delinsGT
NM_000391.4:c.1552-40_1552-39delinsGT MANE Select	NP_000382.3:n.1552-40_1552-39delinsGT