Canonical Allele Identifier: CA1950237752

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617012C= , CM000673.2:g.6617012C=	GRCh38
NC_000011.9:g.6638243C= , CM000673.1:g.6638243C=	GRCh37
NC_000011.8:g.6594819C=	NCBI36
NG_008653.1:g.7450G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.536G=	ENSP00000507321.1:p.Gly179=
ENST00000299427.12:c.650G= MANE Select	ENSP00000299427.6:p.Gly217=
ENST00000436873.7:c.312+289G=
ENST00000524788.2:n.1809G=
ENST00000524903.2:n.1925G=
ENST00000528807.2:n.306G=
ENST00000530040.2:n.479+347G=
ENST00000533371.6:c.-80G=	ENSP00000437066.1:n.-80G=
ENST00000534644.6:n.598G=
ENST00000642892.1:c.-80G=	ENSP00000494165.1:n.-80G=
ENST00000643439.1:c.*390G=	ENSP00000495849.1:n.*390G=
ENST00000643479.1:n.679G=
ENST00000643516.1:c.395+289G=
ENST00000644151.1:n.2089G=
ENST00000644218.1:c.650G=	ENSP00000493574.1:p.Gly217=
ENST00000644683.1:c.*103G=	ENSP00000494085.1:n.*103G=
ENST00000644810.1:c.371G=	ENSP00000495895.1:p.Gly124=
ENST00000644831.1:n.826G=
ENST00000644933.1:c.-80G=	ENSP00000496133.1:n.-80G=
ENST00000645020.1:n.1825G=
ENST00000645285.1:c.-80G=	ENSP00000495058.1:n.-80G=
ENST00000645331.1:n.1016G=
ENST00000645620.1:c.-80G=	ENSP00000493657.1:n.-80G=
ENST00000646777.1:n.826G=
ENST00000647016.1:n.1130G=
ENST00000647152.1:c.-80G=	ENSP00000495893.1:n.-80G=
ENST00000647209.1:c.*519G=	ENSP00000495558.1:n.*519G=
ENST00000647346.1:n.1670G=
ENST00000299427.10:c.650G=	ENSP00000299427.6:p.Gly217=
ENST00000428886.6:n.819G=
ENST00000436873.6:c.450+347G=	ENSP00000398136.2:n.450+347G=
ENST00000524788.1:n.350G=
ENST00000528571.5:c.*390G=	ENSP00000434647.1:n.*390G=
ENST00000528807.1:n.200G=
ENST00000533371.5:c.-80G=	ENSP00000437066.1:n.-80G=
ENST00000534644.5:n.635G=
ENST00000611494.4:c.650G=	ENSP00000484546.1:p.Gly217=
NM_000391.3:c.650G=	NP_000382.3:p.Gly217=
NM_000391.4:c.650G= MANE Select	NP_000382.3:p.Gly217=