Canonical Allele Identifier: CA1950237079

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616655_6616656delinsTA , CM000673.2:g.6616655_6616656delinsTA	GRCh38
NC_000011.9:g.6637886_6637887delinsTA , CM000673.1:g.6637886_6637887delinsTA	GRCh37
NC_000011.8:g.6594462_6594463delinsTA	NCBI36
NG_008653.1:g.7806_7807delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.772+5_772+6delinsTA	ENSP00000507321.1:n.772+5_772+6delinsTA
ENST00000299427.12:c.886+5_886+6delinsTA MANE Select	ENSP00000299427.6:n.886+5_886+6delinsTA
ENST00000436873.7:c.313-582_313-581delinsTA
ENST00000524788.2:n.2050_2051delinsTA
ENST00000524903.2:n.2166_2167delinsTA
ENST00000528807.2:n.547_548delinsTA
ENST00000530040.2:n.480-153_480-152delinsTA
ENST00000533371.6:c.157+5_157+6delinsTA	ENSP00000437066.1:n.157+5_157+6delinsTA
ENST00000642892.1:c.157+5_157+6delinsTA	ENSP00000494165.1:n.157+5_157+6delinsTA
ENST00000643439.1:c.*626+5_*626+6delinsTA	ENSP00000495849.1:n.*626+5_*626+6delinsTA
ENST00000643479.1:n.920_921delinsTA
ENST00000643516.1:c.396-153_396-152delinsTA
ENST00000644151.1:n.2330_2331delinsTA
ENST00000644218.1:c.886+5_886+6delinsTA	ENSP00000493574.1:n.886+5_886+6delinsTA
ENST00000644683.1:c.*339+5_*339+6delinsTA	ENSP00000494085.1:n.*339+5_*339+6delinsTA
ENST00000644810.1:c.607+5_607+6delinsTA	ENSP00000495895.1:n.607+5_607+6delinsTA
ENST00000644831.1:n.1062+5_1062+6delinsTA
ENST00000644933.1:c.157+5_157+6delinsTA	ENSP00000496133.1:n.157+5_157+6delinsTA
ENST00000645020.1:n.2181_2182delinsTA
ENST00000645285.1:c.157+5_157+6delinsTA	ENSP00000495058.1:n.157+5_157+6delinsTA
ENST00000645331.1:n.1257_1258delinsTA
ENST00000645620.1:c.157+5_157+6delinsTA	ENSP00000493657.1:n.157+5_157+6delinsTA
ENST00000646777.1:n.1067_1068delinsTA
ENST00000647016.1:n.1366+5_1366+6delinsTA
ENST00000647152.1:c.157+5_157+6delinsTA	ENSP00000495893.1:n.157+5_157+6delinsTA
ENST00000647209.1:c.*755+5_*755+6delinsTA	ENSP00000495558.1:n.*755+5_*755+6delinsTA
ENST00000647346.1:n.1906+5_1906+6delinsTA
ENST00000299427.10:c.886+5_886+6delinsTA	ENSP00000299427.6:n.886+5_886+6delinsTA
ENST00000436873.6:c.451-153_451-152delinsTA	ENSP00000398136.2:n.451-153_451-152delinsTA
ENST00000528807.1:n.441_442delinsTA
ENST00000533371.5:c.157+5_157+6delinsTA	ENSP00000437066.1:n.157+5_157+6delinsTA
ENST00000611494.4:c.886+5_886+6delinsTA	ENSP00000484546.1:n.886+5_886+6delinsTA
NM_000391.3:c.886+5_886+6delinsTA	NP_000382.3:n.886+5_886+6delinsTA
NM_000391.4:c.886+5_886+6delinsTA MANE Select	NP_000382.3:n.886+5_886+6delinsTA