Canonical Allele Identifier: CA1950236840
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616508_6616514delinsATTTTTT , CM000673.2:g.6616508_6616514delinsATTTTTT GRCh38
NC_000011.9:g.6637739_6637745delinsATTTTTT , CM000673.1:g.6637739_6637745delinsATTTTTT GRCh37
NC_000011.8:g.6594315_6594321delinsATTTTTT NCBI36
NG_008653.1:g.7948_7954delinsAAAAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.773-11_773-5delinsAAAAAAT ENSP00000507321.1:n.773-11_773-5delinsAAAAAAT
ENST00000299427.12:c.887-11_887-5delinsAAAAAAT MANE Select ENSP00000299427.6:n.887-11_887-5delinsAAAAAAT
ENST00000436873.7:c.313-440_313-434delinsAAAAAAT
ENST00000530040.2:n.480-11_480-5delinsAAAAAAT
ENST00000533371.6:c.158-11_158-5delinsAAAAAAT ENSP00000437066.1:n.158-11_158-5delinsAAAAAAT
ENST00000642892.1:c.158-11_158-5delinsAAAAAAT ENSP00000494165.1:n.158-11_158-5delinsAAAAAAT
ENST00000643439.1:c.*627-11_*627-5delinsAAAAAAT ENSP00000495849.1:n.*627-11_*627-5delinsAAAAAAT
ENST00000643479.1:n.1062_1068delinsAAAAAAT
ENST00000643516.1:c.396-11_396-5delinsAAAAAAT
ENST00000644218.1:c.886+147_886+153delinsAAAAAAT ENSP00000493574.1:n.886+147_886+153delinsAAAAAAT
ENST00000644683.1:c.*340-11_*340-5delinsAAAAAAT ENSP00000494085.1:n.*340-11_*340-5delinsAAAAAAT
ENST00000644810.1:c.608-11_608-5delinsAAAAAAT ENSP00000495895.1:n.608-11_608-5delinsAAAAAAT
ENST00000644831.1:n.1063-11_1063-5delinsAAAAAAT
ENST00000644933.1:c.158-11_158-5delinsAAAAAAT ENSP00000496133.1:n.158-11_158-5delinsAAAAAAT
ENST00000645285.1:c.157+147_157+153delinsAAAAAAT ENSP00000495058.1:n.157+147_157+153delinsAAAAAAT
ENST00000645331.1:n.1399_1405delinsAAAAAAT
ENST00000645620.1:c.158-11_158-5delinsAAAAAAT ENSP00000493657.1:n.158-11_158-5delinsAAAAAAT
ENST00000646777.1:n.1209_1215delinsAAAAAAT
ENST00000647016.1:n.1367-11_1367-5delinsAAAAAAT
ENST00000647152.1:c.158-11_158-5delinsAAAAAAT ENSP00000495893.1:n.158-11_158-5delinsAAAAAAT
ENST00000647209.1:c.*756-11_*756-5delinsAAAAAAT ENSP00000495558.1:n.*756-11_*756-5delinsAAAAAAT
ENST00000647346.1:n.1907-11_1907-5delinsAAAAAAT
ENST00000299427.10:c.887-11_887-5delinsAAAAAAT ENSP00000299427.6:n.887-11_887-5delinsAAAAAAT
ENST00000436873.6:c.451-11_451-5delinsAAAAAAT ENSP00000398136.2:n.451-11_451-5delinsAAAAAAT
ENST00000533371.5:c.158-11_158-5delinsAAAAAAT ENSP00000437066.1:n.158-11_158-5delinsAAAAAAT
ENST00000611494.4:c.887-11_887-5delinsAAAAAAT ENSP00000484546.1:n.887-11_887-5delinsAAAAAAT
NM_000391.3:c.887-11_887-5delinsAAAAAAT NP_000382.3:n.887-11_887-5delinsAAAAAAT
NM_000391.4:c.887-11_887-5delinsAAAAAAT MANE Select NP_000382.3:n.887-11_887-5delinsAAAAAAT