Canonical Allele Identifier: CA2612257267

Gene: TPP1

Linked Data

• gnomAD v4: 11-6615538-GCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615541_6615543del , CM000673.2:g.6615541_6615543del	GRCh38
NC_000011.9:g.6636772_6636774del , CM000673.1:g.6636772_6636774del	GRCh37
NC_000011.8:g.6593348_6593350del	NCBI36
NG_008653.1:g.8921_8923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1053_1055del	ENSP00000507321.1:p.Gly352del
ENST00000299427.12:c.1167_1169del MANE Select	ENSP00000299427.6:p.Gly390del
ENST00000436873.7:c.404_406del
ENST00000524924.2:n.287_289del
ENST00000533371.6:c.438_440del	ENSP00000437066.1:p.Gly147del
ENST00000642892.1:c.438_440del	ENSP00000494165.1:p.Gly147del
ENST00000643342.1:c.240_242del
ENST00000643439.1:c.*907_*909del	ENSP00000495849.1:n.*907_*909del
ENST00000643479.1:n.1353_1355del
ENST00000643516.1:c.676_678del
ENST00000644218.1:c.978_980del	ENSP00000493574.1:p.Gly327del
ENST00000644683.1:c.*620_*622del	ENSP00000494085.1:n.*620_*622del
ENST00000644810.1:c.888_890del	ENSP00000495895.1:p.Gly297del
ENST00000644831.1:n.1343_1345del
ENST00000644933.1:c.*33_*35del	ENSP00000496133.1:n.*33_*35del
ENST00000645285.1:c.*33_*35del	ENSP00000495058.1:n.*33_*35del
ENST00000645331.1:n.2372_2374del
ENST00000645620.1:c.438_440del	ENSP00000493657.1:p.Gly147del
ENST00000646691.1:n.942_944del
ENST00000646777.1:n.1500_1502del
ENST00000647016.1:n.1647_1649del
ENST00000647152.1:c.438_440del	ENSP00000495893.1:p.Gly147del
ENST00000647209.1:c.*1036_*1038del	ENSP00000495558.1:n.*1036_*1038del
ENST00000647346.1:n.2187_2189del
ENST00000299427.10:c.1167_1169del	ENSP00000299427.6:p.Gly390del
ENST00000524924.1:n.122_124del
ENST00000532191.1:n.220_222del
ENST00000533371.5:c.438_440del	ENSP00000437066.1:p.Gly147del
ENST00000611494.4:c.1167_1169del	ENSP00000484546.1:p.Gly390del
NM_000391.3:c.1167_1169del	NP_000382.3:p.Gly390del
NM_000391.4:c.1167_1169del MANE Select	NP_000382.3:p.Gly390del