Canonical Allele Identifier: CA2612258058

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616507-GATT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616508_6616510del , CM000673.2:g.6616508_6616510del	GRCh38
NC_000011.9:g.6637739_6637741del , CM000673.1:g.6637739_6637741del	GRCh37
NC_000011.8:g.6594315_6594317del	NCBI36
NG_008653.1:g.7952_7954del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.773-7_773-5del	ENSP00000507321.1:n.773-7_773-5del
ENST00000299427.12:c.887-7_887-5del MANE Select	ENSP00000299427.6:n.887-7_887-5del
ENST00000436873.7:c.313-436_313-434del
ENST00000530040.2:n.480-7_480-5del
ENST00000533371.6:c.158-7_158-5del	ENSP00000437066.1:n.158-7_158-5del
ENST00000642892.1:c.158-7_158-5del	ENSP00000494165.1:n.158-7_158-5del
ENST00000643439.1:c.*627-7_*627-5del	ENSP00000495849.1:n.*627-7_*627-5del
ENST00000643479.1:n.1066_1068del
ENST00000643516.1:c.396-7_396-5del
ENST00000644218.1:c.886+151_886+153del	ENSP00000493574.1:n.886+151_886+153del
ENST00000644683.1:c.*340-7_*340-5del	ENSP00000494085.1:n.*340-7_*340-5del
ENST00000644810.1:c.608-7_608-5del	ENSP00000495895.1:n.608-7_608-5del
ENST00000644831.1:n.1063-7_1063-5del
ENST00000644933.1:c.158-7_158-5del	ENSP00000496133.1:n.158-7_158-5del
ENST00000645285.1:c.157+151_157+153del	ENSP00000495058.1:n.157+151_157+153del
ENST00000645331.1:n.1403_1405del
ENST00000645620.1:c.158-7_158-5del	ENSP00000493657.1:n.158-7_158-5del
ENST00000646777.1:n.1213_1215del
ENST00000647016.1:n.1367-7_1367-5del
ENST00000647152.1:c.158-7_158-5del	ENSP00000495893.1:n.158-7_158-5del
ENST00000647209.1:c.*756-7_*756-5del	ENSP00000495558.1:n.*756-7_*756-5del
ENST00000647346.1:n.1907-7_1907-5del
ENST00000299427.10:c.887-7_887-5del	ENSP00000299427.6:n.887-7_887-5del
ENST00000436873.6:c.451-7_451-5del	ENSP00000398136.2:n.451-7_451-5del
ENST00000533371.5:c.158-7_158-5del	ENSP00000437066.1:n.158-7_158-5del
ENST00000611494.4:c.887-7_887-5del	ENSP00000484546.1:n.887-7_887-5del
NM_000391.3:c.887-7_887-5del	NP_000382.3:n.887-7_887-5del
NM_000391.4:c.887-7_887-5del MANE Select	NP_000382.3:n.887-7_887-5del