Canonical Allele Identifier: CA2612258498

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616863-TGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616868_6616871del , CM000673.2:g.6616868_6616871del	GRCh38
NC_000011.9:g.6638099_6638102del , CM000673.1:g.6638099_6638102del	GRCh37
NC_000011.8:g.6594675_6594678del	NCBI36
NG_008653.1:g.7595_7598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.574-8_574-5del	ENSP00000507321.1:n.574-8_574-5del
ENST00000299427.12:c.688-8_688-5del MANE Select	ENSP00000299427.6:n.688-8_688-5del
ENST00000436873.7:c.312+434_312+437del
ENST00000524788.2:n.1847-8_1847-5del
ENST00000524903.2:n.1963-8_1963-5del
ENST00000528807.2:n.344-8_344-5del
ENST00000530040.2:n.480-364_480-361del
ENST00000533371.6:c.-42-8_-42-5del	ENSP00000437066.1:n.-42-8_-42-5del
ENST00000642892.1:c.-42-8_-42-5del	ENSP00000494165.1:n.-42-8_-42-5del
ENST00000643439.1:c.*428-8_*428-5del	ENSP00000495849.1:n.*428-8_*428-5del
ENST00000643479.1:n.717-8_717-5del
ENST00000643516.1:c.396-364_396-361del
ENST00000644151.1:n.2127-8_2127-5del
ENST00000644218.1:c.688-8_688-5del	ENSP00000493574.1:n.688-8_688-5del
ENST00000644683.1:c.*141-8_*141-5del	ENSP00000494085.1:n.*141-8_*141-5del
ENST00000644810.1:c.409-8_409-5del	ENSP00000495895.1:n.409-8_409-5del
ENST00000644831.1:n.864-8_864-5del
ENST00000644933.1:c.-42-8_-42-5del	ENSP00000496133.1:n.-42-8_-42-5del
ENST00000645020.1:n.1970_1973del
ENST00000645285.1:c.-42-8_-42-5del	ENSP00000495058.1:n.-42-8_-42-5del
ENST00000645331.1:n.1054-8_1054-5del
ENST00000645620.1:c.-42-8_-42-5del	ENSP00000493657.1:n.-42-8_-42-5del
ENST00000646777.1:n.864-8_864-5del
ENST00000647016.1:n.1168-8_1168-5del
ENST00000647152.1:c.-42-8_-42-5del	ENSP00000495893.1:n.-42-8_-42-5del
ENST00000647209.1:c.*557-8_*557-5del	ENSP00000495558.1:n.*557-8_*557-5del
ENST00000647346.1:n.1708-8_1708-5del
ENST00000299427.10:c.688-8_688-5del	ENSP00000299427.6:n.688-8_688-5del
ENST00000436873.6:c.451-364_451-361del	ENSP00000398136.2:n.451-364_451-361del
ENST00000524788.1:n.388-8_388-5del
ENST00000528807.1:n.238-8_238-5del
ENST00000533371.5:c.-42-8_-42-5del	ENSP00000437066.1:n.-42-8_-42-5del
ENST00000611494.4:c.688-8_688-5del	ENSP00000484546.1:n.688-8_688-5del
NM_000391.3:c.688-8_688-5del	NP_000382.3:n.688-8_688-5del
NM_000391.4:c.688-8_688-5del MANE Select	NP_000382.3:n.688-8_688-5del