Canonical Allele Identifier: CA1950236829
Gene: TPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1589948296
gnomAD v4: 11-6616508-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616508A>T , CM000673.2:g.6616508A>T GRCh38
NC_000011.9:g.6637739A>T , CM000673.1:g.6637739A>T GRCh37
NC_000011.8:g.6594315A>T NCBI36
NG_008653.1:g.7954T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.773-5T>A ENSP00000507321.1:n.773-5T>A
ENST00000299427.12:c.887-5T>A MANE Select ENSP00000299427.6:n.887-5T>A
ENST00000436873.7:c.313-434T>A
ENST00000530040.2:n.480-5T>A
ENST00000533371.6:c.158-5T>A ENSP00000437066.1:n.158-5T>A
ENST00000642892.1:c.158-5T>A ENSP00000494165.1:n.158-5T>A
ENST00000643439.1:c.*627-5T>A ENSP00000495849.1:n.*627-5T>A
ENST00000643479.1:n.1068T>A
ENST00000643516.1:c.396-5T>A
ENST00000644218.1:c.886+153T>A ENSP00000493574.1:n.886+153T>A
ENST00000644683.1:c.*340-5T>A ENSP00000494085.1:n.*340-5T>A
ENST00000644810.1:c.608-5T>A ENSP00000495895.1:n.608-5T>A
ENST00000644831.1:n.1063-5T>A
ENST00000644933.1:c.158-5T>A ENSP00000496133.1:n.158-5T>A
ENST00000645285.1:c.157+153T>A ENSP00000495058.1:n.157+153T>A
ENST00000645331.1:n.1405T>A
ENST00000645620.1:c.158-5T>A ENSP00000493657.1:n.158-5T>A
ENST00000646777.1:n.1215T>A
ENST00000647016.1:n.1367-5T>A
ENST00000647152.1:c.158-5T>A ENSP00000495893.1:n.158-5T>A
ENST00000647209.1:c.*756-5T>A ENSP00000495558.1:n.*756-5T>A
ENST00000647346.1:n.1907-5T>A
ENST00000299427.10:c.887-5T>A ENSP00000299427.6:n.887-5T>A
ENST00000436873.6:c.451-5T>A ENSP00000398136.2:n.451-5T>A
ENST00000533371.5:c.158-5T>A ENSP00000437066.1:n.158-5T>A
ENST00000611494.4:c.887-5T>A ENSP00000484546.1:n.887-5T>A
NM_000391.3:c.887-5T>A NP_000382.3:n.887-5T>A
NM_000391.4:c.887-5T>A MANE Select NP_000382.3:n.887-5T>A