Canonical Allele Identifier: CA1950237893

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617055_6617056delinsAG , CM000673.2:g.6617055_6617056delinsAG	GRCh38
NC_000011.9:g.6638286_6638287delinsAG , CM000673.1:g.6638286_6638287delinsAG	GRCh37
NC_000011.8:g.6594862_6594863delinsAG	NCBI36
NG_008653.1:g.7406_7407delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.492_493delinsCT	ENSP00000507321.1:p.Pro164=
ENST00000299427.12:c.606_607delinsCT MANE Select	ENSP00000299427.6:p.Pro202=
ENST00000436873.7:c.312+245_312+246delinsCT
ENST00000524788.2:n.1765_1766delinsCT
ENST00000524903.2:n.1881_1882delinsCT
ENST00000528807.2:n.262_263delinsCT
ENST00000530040.2:n.479+303_479+304delinsCT
ENST00000533371.6:c.-124_-123delinsCT	ENSP00000437066.1:n.-124_-123delinsCT
ENST00000534644.6:n.554_555delinsCT
ENST00000642892.1:c.-124_-123delinsCT	ENSP00000494165.1:n.-124_-123delinsCT
ENST00000643439.1:c.*346_*347delinsCT	ENSP00000495849.1:n.*346_*347delinsCT
ENST00000643479.1:n.635_636delinsCT
ENST00000643516.1:c.395+245_395+246delinsCT
ENST00000644151.1:n.2045_2046delinsCT
ENST00000644218.1:c.606_607delinsCT	ENSP00000493574.1:p.Pro202=
ENST00000644683.1:c.*59_*60delinsCT	ENSP00000494085.1:n.*59_*60delinsCT
ENST00000644810.1:c.327_328delinsCT	ENSP00000495895.1:p.Pro109=
ENST00000644831.1:n.782_783delinsCT
ENST00000644933.1:c.-124_-123delinsCT	ENSP00000496133.1:n.-124_-123delinsCT
ENST00000645020.1:n.1781_1782delinsCT
ENST00000645285.1:c.-124_-123delinsCT	ENSP00000495058.1:n.-124_-123delinsCT
ENST00000645331.1:n.972_973delinsCT
ENST00000645620.1:c.-124_-123delinsCT	ENSP00000493657.1:n.-124_-123delinsCT
ENST00000646777.1:n.782_783delinsCT
ENST00000647016.1:n.1086_1087delinsCT
ENST00000647152.1:c.-124_-123delinsCT	ENSP00000495893.1:n.-124_-123delinsCT
ENST00000647209.1:c.*475_*476delinsCT	ENSP00000495558.1:n.*475_*476delinsCT
ENST00000647346.1:n.1626_1627delinsCT
ENST00000299427.10:c.606_607delinsCT	ENSP00000299427.6:p.Pro202=
ENST00000428886.6:n.775_776delinsCT
ENST00000436873.6:c.450+303_450+304delinsCT	ENSP00000398136.2:n.450+303_450+304delinsCT
ENST00000524788.1:n.306_307delinsCT
ENST00000528571.5:c.*346_*347delinsCT	ENSP00000434647.1:n.*346_*347delinsCT
ENST00000528807.1:n.156_157delinsCT
ENST00000533371.5:c.-124_-123delinsCT	ENSP00000437066.1:n.-124_-123delinsCT
ENST00000534644.5:n.591_592delinsCT
ENST00000611494.4:c.606_607delinsCT	ENSP00000484546.1:p.Pro202=
NM_000391.3:c.606_607delinsCT	NP_000382.3:p.Pro202=
NM_000391.4:c.606_607delinsCT MANE Select	NP_000382.3:p.Pro202=