Canonical Allele Identifier: CA2790314305

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616556_6616562del , CM000673.2:g.6616556_6616562del	GRCh38
NC_000011.9:g.6637787_6637793del , CM000673.1:g.6637787_6637793del	GRCh37
NC_000011.8:g.6594363_6594369del	NCBI36
NG_008653.1:g.7902_7908del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-57_773-51del	ENSP00000507321.1:n.773-57_773-51del
ENST00000299427.12:c.887-57_887-51del MANE Select	ENSP00000299427.6:n.887-57_887-51del
ENST00000436873.7:c.313-486_313-480del
ENST00000524903.2:n.2262_2268del
ENST00000528807.2:n.643_649del
ENST00000530040.2:n.480-57_480-51del
ENST00000533371.6:c.158-57_158-51del	ENSP00000437066.1:n.158-57_158-51del
ENST00000642892.1:c.158-57_158-51del	ENSP00000494165.1:n.158-57_158-51del
ENST00000643439.1:c.*627-57_*627-51del	ENSP00000495849.1:n.*627-57_*627-51del
ENST00000643479.1:n.1016_1022del
ENST00000643516.1:c.396-57_396-51del
ENST00000644218.1:c.886+101_886+107del	ENSP00000493574.1:n.886+101_886+107del
ENST00000644683.1:c.*340-57_*340-51del	ENSP00000494085.1:n.*340-57_*340-51del
ENST00000644810.1:c.608-57_608-51del	ENSP00000495895.1:n.608-57_608-51del
ENST00000644831.1:n.1063-57_1063-51del
ENST00000644933.1:c.158-57_158-51del	ENSP00000496133.1:n.158-57_158-51del
ENST00000645020.1:n.2277_2283del
ENST00000645285.1:c.157+101_157+107del	ENSP00000495058.1:n.157+101_157+107del
ENST00000645331.1:n.1353_1359del
ENST00000645620.1:c.158-57_158-51del	ENSP00000493657.1:n.158-57_158-51del
ENST00000646777.1:n.1163_1169del
ENST00000647016.1:n.1367-57_1367-51del
ENST00000647152.1:c.158-57_158-51del	ENSP00000495893.1:n.158-57_158-51del
ENST00000647209.1:c.*756-57_*756-51del	ENSP00000495558.1:n.*756-57_*756-51del
ENST00000647346.1:n.1907-57_1907-51del
ENST00000299427.10:c.887-57_887-51del	ENSP00000299427.6:n.887-57_887-51del
ENST00000436873.6:c.451-57_451-51del	ENSP00000398136.2:n.451-57_451-51del
ENST00000528807.1:n.537_543del
ENST00000533371.5:c.158-57_158-51del	ENSP00000437066.1:n.158-57_158-51del
ENST00000611494.4:c.887-57_887-51del	ENSP00000484546.1:n.887-57_887-51del
NM_000391.3:c.887-57_887-51del	NP_000382.3:n.887-57_887-51del
NM_000391.4:c.887-57_887-51del MANE Select	NP_000382.3:n.887-57_887-51del