Canonical Allele Identifier: CA1950237638

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616951C= , CM000673.2:g.6616951C=	GRCh38
NC_000011.9:g.6638182C= , CM000673.1:g.6638182C=	GRCh37
NC_000011.8:g.6594758C=	NCBI36
NG_008653.1:g.7511G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.573+24G=	ENSP00000507321.1:n.573+24G=
ENST00000299427.12:c.687+24G= MANE Select	ENSP00000299427.6:n.687+24G=
ENST00000436873.7:c.312+350G=
ENST00000524788.2:n.1846+24G=
ENST00000524903.2:n.1962+24G=
ENST00000528807.2:n.343+24G=
ENST00000530040.2:n.479+408G=
ENST00000533371.6:c.-43+24G=	ENSP00000437066.1:n.-43+24G=
ENST00000642892.1:c.-43+24G=	ENSP00000494165.1:n.-43+24G=
ENST00000643439.1:c.*427+24G=	ENSP00000495849.1:n.*427+24G=
ENST00000643479.1:n.716+24G=
ENST00000643516.1:c.395+350G=
ENST00000644151.1:n.2126+24G=
ENST00000644218.1:c.687+24G=	ENSP00000493574.1:n.687+24G=
ENST00000644683.1:c.*140+24G=	ENSP00000494085.1:n.*140+24G=
ENST00000644810.1:c.408+24G=	ENSP00000495895.1:n.408+24G=
ENST00000644831.1:n.863+24G=
ENST00000644933.1:c.-43+24G=	ENSP00000496133.1:n.-43+24G=
ENST00000645020.1:n.1886G=
ENST00000645285.1:c.-43+24G=	ENSP00000495058.1:n.-43+24G=
ENST00000645331.1:n.1053+24G=
ENST00000645620.1:c.-43+24G=	ENSP00000493657.1:n.-43+24G=
ENST00000646777.1:n.863+24G=
ENST00000647016.1:n.1167+24G=
ENST00000647152.1:c.-43+24G=	ENSP00000495893.1:n.-43+24G=
ENST00000647209.1:c.*556+24G=	ENSP00000495558.1:n.*556+24G=
ENST00000647346.1:n.1707+24G=
ENST00000299427.10:c.687+24G=	ENSP00000299427.6:n.687+24G=
ENST00000436873.6:c.450+408G=	ENSP00000398136.2:n.450+408G=
ENST00000524788.1:n.387+24G=
ENST00000528807.1:n.237+24G=
ENST00000533371.5:c.-43+24G=	ENSP00000437066.1:n.-43+24G=
ENST00000611494.4:c.687+24G=	ENSP00000484546.1:n.687+24G=
NM_000391.3:c.687+24G=	NP_000382.3:n.687+24G=
NM_000391.4:c.687+24G= MANE Select	NP_000382.3:n.687+24G=