Canonical Allele Identifier: CA2790314284
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616524_6616528dup , CM000673.2:g.6616524_6616528dup GRCh38
NC_000011.9:g.6637755_6637759dup , CM000673.1:g.6637755_6637759dup GRCh37
NC_000011.8:g.6594331_6594335dup NCBI36
NG_008653.1:g.7949_7953dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682424.1:c.773-10_773-6dup ENSP00000507321.1:n.773-10_773-6dup
ENST00000299427.12:c.887-10_887-6dup MANE Select ENSP00000299427.6:n.887-10_887-6dup
ENST00000436873.7:c.313-439_313-435dup
ENST00000530040.2:n.480-10_480-6dup
ENST00000533371.6:c.158-10_158-6dup ENSP00000437066.1:n.158-10_158-6dup
ENST00000642892.1:c.158-10_158-6dup ENSP00000494165.1:n.158-10_158-6dup
ENST00000643439.1:c.*627-10_*627-6dup ENSP00000495849.1:n.*627-10_*627-6dup
ENST00000643479.1:n.1063_1067dup
ENST00000643516.1:c.396-10_396-6dup
ENST00000644218.1:c.886+148_886+152dup ENSP00000493574.1:n.886+148_886+152dup
ENST00000644683.1:c.*340-10_*340-6dup ENSP00000494085.1:n.*340-10_*340-6dup
ENST00000644810.1:c.608-10_608-6dup ENSP00000495895.1:n.608-10_608-6dup
ENST00000644831.1:n.1063-10_1063-6dup
ENST00000644933.1:c.158-10_158-6dup ENSP00000496133.1:n.158-10_158-6dup
ENST00000645285.1:c.157+148_157+152dup ENSP00000495058.1:n.157+148_157+152dup
ENST00000645331.1:n.1400_1404dup
ENST00000645620.1:c.158-10_158-6dup ENSP00000493657.1:n.158-10_158-6dup
ENST00000646777.1:n.1210_1214dup
ENST00000647016.1:n.1367-10_1367-6dup
ENST00000647152.1:c.158-10_158-6dup ENSP00000495893.1:n.158-10_158-6dup
ENST00000647209.1:c.*756-10_*756-6dup ENSP00000495558.1:n.*756-10_*756-6dup
ENST00000647346.1:n.1907-10_1907-6dup
ENST00000299427.10:c.887-10_887-6dup ENSP00000299427.6:n.887-10_887-6dup
ENST00000436873.6:c.451-10_451-6dup ENSP00000398136.2:n.451-10_451-6dup
ENST00000533371.5:c.158-10_158-6dup ENSP00000437066.1:n.158-10_158-6dup
ENST00000611494.4:c.887-10_887-6dup ENSP00000484546.1:n.887-10_887-6dup
NM_000391.3:c.887-10_887-6dup NP_000382.3:n.887-10_887-6dup
NM_000391.4:c.887-10_887-6dup MANE Select NP_000382.3:n.887-10_887-6dup