Canonical Allele Identifier: CA2612258067

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616525-TTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616526_6616529del , CM000673.2:g.6616526_6616529del	GRCh38
NC_000011.9:g.6637757_6637760del , CM000673.1:g.6637757_6637760del	GRCh37
NC_000011.8:g.6594333_6594336del	NCBI36
NG_008653.1:g.7933_7936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-26_773-23del	ENSP00000507321.1:n.773-26_773-23del
ENST00000299427.12:c.887-26_887-23del MANE Select	ENSP00000299427.6:n.887-26_887-23del
ENST00000436873.7:c.313-455_313-452del
ENST00000524903.2:n.2293_2296del
ENST00000530040.2:n.480-26_480-23del
ENST00000533371.6:c.158-26_158-23del	ENSP00000437066.1:n.158-26_158-23del
ENST00000642892.1:c.158-26_158-23del	ENSP00000494165.1:n.158-26_158-23del
ENST00000643439.1:c.*627-26_*627-23del	ENSP00000495849.1:n.*627-26_*627-23del
ENST00000643479.1:n.1047_1050del
ENST00000643516.1:c.396-26_396-23del
ENST00000644218.1:c.886+132_886+135del	ENSP00000493574.1:n.886+132_886+135del
ENST00000644683.1:c.*340-26_*340-23del	ENSP00000494085.1:n.*340-26_*340-23del
ENST00000644810.1:c.608-26_608-23del	ENSP00000495895.1:n.608-26_608-23del
ENST00000644831.1:n.1063-26_1063-23del
ENST00000644933.1:c.158-26_158-23del	ENSP00000496133.1:n.158-26_158-23del
ENST00000645285.1:c.157+132_157+135del	ENSP00000495058.1:n.157+132_157+135del
ENST00000645331.1:n.1384_1387del
ENST00000645620.1:c.158-26_158-23del	ENSP00000493657.1:n.158-26_158-23del
ENST00000646777.1:n.1194_1197del
ENST00000647016.1:n.1367-26_1367-23del
ENST00000647152.1:c.158-26_158-23del	ENSP00000495893.1:n.158-26_158-23del
ENST00000647209.1:c.*756-26_*756-23del	ENSP00000495558.1:n.*756-26_*756-23del
ENST00000647346.1:n.1907-26_1907-23del
ENST00000299427.10:c.887-26_887-23del	ENSP00000299427.6:n.887-26_887-23del
ENST00000436873.6:c.451-26_451-23del	ENSP00000398136.2:n.451-26_451-23del
ENST00000528807.1:n.568_571del
ENST00000533371.5:c.158-26_158-23del	ENSP00000437066.1:n.158-26_158-23del
ENST00000611494.4:c.887-26_887-23del	ENSP00000484546.1:n.887-26_887-23del
NM_000391.3:c.887-26_887-23del	NP_000382.3:n.887-26_887-23del
NM_000391.4:c.887-26_887-23del MANE Select	NP_000382.3:n.887-26_887-23del