Canonical Allele Identifier: CA2612255884
Gene: TPP1 HGNC NCBI

Linked Data

gnomAD v4: 11-6617225-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6617225A>C , CM000673.2:g.6617225A>C GRCh38
NC_000011.9:g.6638456A>C , CM000673.1:g.6638456A>C GRCh37
NC_000011.8:g.6595032A>C NCBI36
NG_008653.1:g.7237T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.395-72T>G ENSP00000507321.1:n.395-72T>G
ENST00000299427.12:c.509-72T>G MANE Select ENSP00000299427.6:n.509-72T>G
ENST00000428886.7:n.672T>G
ENST00000436873.7:c.312+76T>G
ENST00000524788.2:n.1596T>G
ENST00000524903.2:n.1712T>G
ENST00000528571.6:c.*324T>G ENSP00000434647.1:n.*324T>G
ENST00000528807.2:n.165-72T>G
ENST00000530040.2:n.479+134T>G
ENST00000533371.6:c.-221-72T>G ENSP00000437066.1:n.-221-72T>G
ENST00000534644.6:n.457-72T>G
ENST00000642892.1:c.-221-72T>G ENSP00000494165.1:n.-221-72T>G
ENST00000643439.1:c.*249-72T>G ENSP00000495849.1:n.*249-72T>G
ENST00000643479.1:n.538-72T>G
ENST00000643516.1:c.395+76T>G
ENST00000644151.1:n.1876T>G
ENST00000644218.1:c.509-72T>G ENSP00000493574.1:n.509-72T>G
ENST00000644683.1:c.451-72T>G ENSP00000494085.1:n.451-72T>G
ENST00000644810.1:c.230-72T>G ENSP00000495895.1:n.230-72T>G
ENST00000644831.1:n.613T>G
ENST00000644933.1:c.-221-72T>G ENSP00000496133.1:n.-221-72T>G
ENST00000645020.1:n.1612T>G
ENST00000645285.1:c.-221-72T>G ENSP00000495058.1:n.-221-72T>G
ENST00000645331.1:n.803T>G
ENST00000645620.1:c.-221-72T>G ENSP00000493657.1:n.-221-72T>G
ENST00000646777.1:n.613T>G
ENST00000647016.1:n.917T>G
ENST00000647152.1:c.-221-72T>G ENSP00000495893.1:n.-221-72T>G
ENST00000647209.1:c.*378-72T>G ENSP00000495558.1:n.*378-72T>G
ENST00000647346.1:n.1529-72T>G
ENST00000299427.10:c.509-72T>G ENSP00000299427.6:n.509-72T>G
ENST00000428886.6:n.606T>G
ENST00000436873.6:c.450+134T>G ENSP00000398136.2:n.450+134T>G
ENST00000524788.1:n.137T>G
ENST00000528571.5:c.*249-72T>G ENSP00000434647.1:n.*249-72T>G
ENST00000533371.5:c.-221-72T>G ENSP00000437066.1:n.-221-72T>G
ENST00000534644.5:n.494-72T>G
ENST00000611494.4:c.509-72T>G ENSP00000484546.1:n.509-72T>G
NM_000391.3:c.509-72T>G NP_000382.3:n.509-72T>G
NM_000391.4:c.509-72T>G MANE Select NP_000382.3:n.509-72T>G