Canonical Allele Identifier: CA2790314279
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616503_6616504insA , CM000673.2:g.6616503_6616504insA GRCh38
NC_000011.9:g.6637734_6637735insA , CM000673.1:g.6637734_6637735insA GRCh37
NC_000011.8:g.6594310_6594311insA NCBI36
NG_008653.1:g.7958_7959insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.773-1_773insT ENSP00000507321.1:n.773-1_773insT
ENST00000299427.12:c.887-1_887insT MANE Select ENSP00000299427.6:n.887-1_887insT
ENST00000436873.7:c.313-430_313-429insT
ENST00000530040.2:n.480-1_480insT
ENST00000533371.6:c.158-1_158insT ENSP00000437066.1:n.158-1_158insT
ENST00000642892.1:c.158-1_158insT ENSP00000494165.1:n.158-1_158insT
ENST00000643439.1:c.*627-1_*627insT ENSP00000495849.1:n.*627-1_*627insT
ENST00000643479.1:n.1072_1073insT
ENST00000643516.1:c.396-1_396insT
ENST00000644218.1:c.886+157_886+158insT ENSP00000493574.1:n.886+157_886+158insT
ENST00000644683.1:c.*340-1_*340insT ENSP00000494085.1:n.*340-1_*340insT
ENST00000644810.1:c.608-1_608insT ENSP00000495895.1:n.608-1_608insT
ENST00000644831.1:n.1063-1_1063insT
ENST00000644933.1:c.158-1_158insT ENSP00000496133.1:n.158-1_158insT
ENST00000645285.1:c.157+157_157+158insT ENSP00000495058.1:n.157+157_157+158insT
ENST00000645331.1:n.1409_1410insT
ENST00000645620.1:c.158-1_158insT ENSP00000493657.1:n.158-1_158insT
ENST00000646777.1:n.1219_1220insT
ENST00000647016.1:n.1367-1_1367insT
ENST00000647152.1:c.158-1_158insT ENSP00000495893.1:n.158-1_158insT
ENST00000647209.1:c.*756-1_*756insT ENSP00000495558.1:n.*756-1_*756insT
ENST00000647346.1:n.1907-1_1907insT
ENST00000299427.10:c.887-1_887insT ENSP00000299427.6:n.887-1_887insT
ENST00000436873.6:c.451-1_451insT ENSP00000398136.2:n.451-1_451insT
ENST00000533371.5:c.158-1_158insT ENSP00000437066.1:n.158-1_158insT
ENST00000611494.4:c.887-1_887insT ENSP00000484546.1:n.887-1_887insT
NM_000391.3:c.887-1_887insT NP_000382.3:n.887-1_887insT
NM_000391.4:c.887-1_887insT MANE Select NP_000382.3:n.887-1_887insT