Canonical Allele Identifier: CA2497029228

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616508_6616510delinsATT , CM000673.2:g.6616508_6616510delinsATT	GRCh38
NC_000011.9:g.6637739_6637741delinsATT , CM000673.1:g.6637739_6637741delinsATT	GRCh37
NC_000011.8:g.6594315_6594317delinsATT	NCBI36
NG_008653.1:g.7952_7954delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-7_773-5delinsAAT	ENSP00000507321.1:n.773-7_773-5delinsAAT
ENST00000299427.12:c.887-7_887-5delinsAAT MANE Select	ENSP00000299427.6:n.887-7_887-5delinsAAT
ENST00000436873.7:c.313-436_313-434delinsAAT
ENST00000530040.2:n.480-7_480-5delinsAAT
ENST00000533371.6:c.158-7_158-5delinsAAT	ENSP00000437066.1:n.158-7_158-5delinsAAT
ENST00000642892.1:c.158-7_158-5delinsAAT	ENSP00000494165.1:n.158-7_158-5delinsAAT
ENST00000643439.1:c.*627-7_*627-5delinsAAT	ENSP00000495849.1:n.*627-7_*627-5delinsAAT
ENST00000643479.1:n.1066_1068delinsAAT
ENST00000643516.1:c.396-7_396-5delinsAAT
ENST00000644218.1:c.886+151_886+153delinsAAT	ENSP00000493574.1:n.886+151_886+153delinsAAT
ENST00000644683.1:c.*340-7_*340-5delinsAAT	ENSP00000494085.1:n.*340-7_*340-5delinsAAT
ENST00000644810.1:c.608-7_608-5delinsAAT	ENSP00000495895.1:n.608-7_608-5delinsAAT
ENST00000644831.1:n.1063-7_1063-5delinsAAT
ENST00000644933.1:c.158-7_158-5delinsAAT	ENSP00000496133.1:n.158-7_158-5delinsAAT
ENST00000645285.1:c.157+151_157+153delinsAAT	ENSP00000495058.1:n.157+151_157+153delinsAAT
ENST00000645331.1:n.1403_1405delinsAAT
ENST00000645620.1:c.158-7_158-5delinsAAT	ENSP00000493657.1:n.158-7_158-5delinsAAT
ENST00000646777.1:n.1213_1215delinsAAT
ENST00000647016.1:n.1367-7_1367-5delinsAAT
ENST00000647152.1:c.158-7_158-5delinsAAT	ENSP00000495893.1:n.158-7_158-5delinsAAT
ENST00000647209.1:c.*756-7_*756-5delinsAAT	ENSP00000495558.1:n.*756-7_*756-5delinsAAT
ENST00000647346.1:n.1907-7_1907-5delinsAAT
ENST00000299427.10:c.887-7_887-5delinsAAT	ENSP00000299427.6:n.887-7_887-5delinsAAT
ENST00000436873.6:c.451-7_451-5delinsAAT	ENSP00000398136.2:n.451-7_451-5delinsAAT
ENST00000533371.5:c.158-7_158-5delinsAAT	ENSP00000437066.1:n.158-7_158-5delinsAAT
ENST00000611494.4:c.887-7_887-5delinsAAT	ENSP00000484546.1:n.887-7_887-5delinsAAT
NM_000391.3:c.887-7_887-5delinsAAT	NP_000382.3:n.887-7_887-5delinsAAT
NM_000391.4:c.887-7_887-5delinsAAT MANE Select	NP_000382.3:n.887-7_887-5delinsAAT