Canonical Allele Identifier: CA2574741277

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616508-A-ATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616526_6616528dup , CM000673.2:g.6616526_6616528dup	GRCh38
NC_000011.9:g.6637757_6637759dup , CM000673.1:g.6637757_6637759dup	GRCh37
NC_000011.8:g.6594333_6594335dup	NCBI36
NG_008653.1:g.7951_7953dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-8_773-6dup	ENSP00000507321.1:n.773-8_773-6dup
ENST00000299427.12:c.887-8_887-6dup MANE Select	ENSP00000299427.6:n.887-8_887-6dup
ENST00000436873.7:c.313-437_313-435dup
ENST00000530040.2:n.480-8_480-6dup
ENST00000533371.6:c.158-8_158-6dup	ENSP00000437066.1:n.158-8_158-6dup
ENST00000642892.1:c.158-8_158-6dup	ENSP00000494165.1:n.158-8_158-6dup
ENST00000643439.1:c.*627-8_*627-6dup	ENSP00000495849.1:n.*627-8_*627-6dup
ENST00000643479.1:n.1065_1067dup
ENST00000643516.1:c.396-8_396-6dup
ENST00000644218.1:c.886+150_886+152dup	ENSP00000493574.1:n.886+150_886+152dup
ENST00000644683.1:c.*340-8_*340-6dup	ENSP00000494085.1:n.*340-8_*340-6dup
ENST00000644810.1:c.608-8_608-6dup	ENSP00000495895.1:n.608-8_608-6dup
ENST00000644831.1:n.1063-8_1063-6dup
ENST00000644933.1:c.158-8_158-6dup	ENSP00000496133.1:n.158-8_158-6dup
ENST00000645285.1:c.157+150_157+152dup	ENSP00000495058.1:n.157+150_157+152dup
ENST00000645331.1:n.1402_1404dup
ENST00000645620.1:c.158-8_158-6dup	ENSP00000493657.1:n.158-8_158-6dup
ENST00000646777.1:n.1212_1214dup
ENST00000647016.1:n.1367-8_1367-6dup
ENST00000647152.1:c.158-8_158-6dup	ENSP00000495893.1:n.158-8_158-6dup
ENST00000647209.1:c.*756-8_*756-6dup	ENSP00000495558.1:n.*756-8_*756-6dup
ENST00000647346.1:n.1907-8_1907-6dup
ENST00000299427.10:c.887-8_887-6dup	ENSP00000299427.6:n.887-8_887-6dup
ENST00000436873.6:c.451-8_451-6dup	ENSP00000398136.2:n.451-8_451-6dup
ENST00000533371.5:c.158-8_158-6dup	ENSP00000437066.1:n.158-8_158-6dup
ENST00000611494.4:c.887-8_887-6dup	ENSP00000484546.1:n.887-8_887-6dup
NM_000391.3:c.887-8_887-6dup	NP_000382.3:n.887-8_887-6dup
NM_000391.4:c.887-8_887-6dup MANE Select	NP_000382.3:n.887-8_887-6dup