Canonical Allele Identifier: CA2790314266
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616194C>A , CM000673.2:g.6616194C>A GRCh38
NC_000011.9:g.6637425C>A , CM000673.1:g.6637425C>A GRCh37
NC_000011.8:g.6594001C>A NCBI36
NG_008653.1:g.8268G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.962-120G>T ENSP00000507321.1:n.962-120G>T
ENST00000299427.12:c.1076-120G>T MANE Select ENSP00000299427.6:n.1076-120G>T
ENST00000436873.7:c.313-120G>T
ENST00000524924.2:n.76G>T
ENST00000533371.6:c.347-120G>T ENSP00000437066.1:n.347-120G>T
ENST00000642892.1:c.347-120G>T ENSP00000494165.1:n.347-120G>T
ENST00000643342.1:c.166-120G>T
ENST00000643439.1:c.*816-120G>T ENSP00000495849.1:n.*816-120G>T
ENST00000643479.1:n.1262-120G>T
ENST00000643516.1:c.585-120G>T
ENST00000644218.1:c.887-120G>T ENSP00000493574.1:n.887-120G>T
ENST00000644683.1:c.*529-120G>T ENSP00000494085.1:n.*529-120G>T
ENST00000644810.1:c.797-120G>T ENSP00000495895.1:n.797-120G>T
ENST00000644831.1:n.1252-120G>T
ENST00000644933.1:c.347-120G>T ENSP00000496133.1:n.347-120G>T
ENST00000645285.1:c.158-120G>T ENSP00000495058.1:n.158-120G>T
ENST00000645331.1:n.1719G>T
ENST00000645620.1:c.347-120G>T ENSP00000493657.1:n.347-120G>T
ENST00000646691.1:n.289G>T
ENST00000646777.1:n.1409-120G>T
ENST00000647016.1:n.1556-120G>T
ENST00000647152.1:c.347-120G>T ENSP00000495893.1:n.347-120G>T
ENST00000647209.1:c.*945-120G>T ENSP00000495558.1:n.*945-120G>T
ENST00000647346.1:n.2096-120G>T
ENST00000299427.10:c.1076-120G>T ENSP00000299427.6:n.1076-120G>T
ENST00000533371.5:c.347-120G>T ENSP00000437066.1:n.347-120G>T
ENST00000611494.4:c.1076-120G>T ENSP00000484546.1:n.1076-120G>T
NM_000391.3:c.1076-120G>T NP_000382.3:n.1076-120G>T
NM_000391.4:c.1076-120G>T MANE Select NP_000382.3:n.1076-120G>T