Canonical Allele Identifier: CA1950232890

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614722_6614723delinsAG , CM000673.2:g.6614722_6614723delinsAG	GRCh38
NC_000011.9:g.6635953_6635954delinsAG , CM000673.1:g.6635953_6635954delinsAG	GRCh37
NC_000011.8:g.6592529_6592530delinsAG	NCBI36
NG_008653.1:g.9739_9740delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1438-37_1438-36delinsCT	ENSP00000507321.1:n.1438-37_1438-36delinsCT
ENST00000299427.12:c.1552-37_1552-36delinsCT MANE Select	ENSP00000299427.6:n.1552-37_1552-36delinsCT
ENST00000524611.2:n.554_555delinsCT
ENST00000524924.2:n.672-37_672-36delinsCT
ENST00000533371.6:c.823-37_823-36delinsCT	ENSP00000437066.1:n.823-37_823-36delinsCT
ENST00000642892.1:c.823-37_823-36delinsCT	ENSP00000494165.1:n.823-37_823-36delinsCT
ENST00000643342.1:c.625-37_625-36delinsCT
ENST00000643439.1:c.*1292-37_*1292-36delinsCT	ENSP00000495849.1:n.*1292-37_*1292-36delinsCT
ENST00000643479.1:n.1738-37_1738-36delinsCT
ENST00000643516.1:c.1061-37_1061-36delinsCT
ENST00000644218.1:c.1363-37_1363-36delinsCT	ENSP00000493574.1:n.1363-37_1363-36delinsCT
ENST00000644683.1:c.*1005-37_*1005-36delinsCT	ENSP00000494085.1:n.*1005-37_*1005-36delinsCT
ENST00000644810.1:c.1273-37_1273-36delinsCT	ENSP00000495895.1:n.1273-37_1273-36delinsCT
ENST00000644831.1:n.1728-37_1728-36delinsCT
ENST00000644933.1:c.*418-37_*418-36delinsCT	ENSP00000496133.1:n.*418-37_*418-36delinsCT
ENST00000645285.1:c.*418-37_*418-36delinsCT	ENSP00000495058.1:n.*418-37_*418-36delinsCT
ENST00000645331.1:n.2757-37_2757-36delinsCT
ENST00000645620.1:c.823-37_823-36delinsCT	ENSP00000493657.1:n.823-37_823-36delinsCT
ENST00000646691.1:n.1439-37_1439-36delinsCT
ENST00000646777.1:n.1885-37_1885-36delinsCT
ENST00000647016.1:n.2032-37_2032-36delinsCT
ENST00000647152.1:c.823-37_823-36delinsCT	ENSP00000495893.1:n.823-37_823-36delinsCT
ENST00000647209.1:c.*1421-37_*1421-36delinsCT	ENSP00000495558.1:n.*1421-37_*1421-36delinsCT
ENST00000647346.1:n.2572-37_2572-36delinsCT
ENST00000299427.10:c.1552-37_1552-36delinsCT	ENSP00000299427.6:n.1552-37_1552-36delinsCT
ENST00000524611.1:n.430-37_430-36delinsCT
ENST00000533371.5:c.823-37_823-36delinsCT	ENSP00000437066.1:n.823-37_823-36delinsCT
ENST00000611494.4:c.1552-37_1552-36delinsCT	ENSP00000484546.1:n.1552-37_1552-36delinsCT
NM_000391.3:c.1552-37_1552-36delinsCT	NP_000382.3:n.1552-37_1552-36delinsCT
NM_000391.4:c.1552-37_1552-36delinsCT MANE Select	NP_000382.3:n.1552-37_1552-36delinsCT