Canonical Allele Identifier: CA1950238185

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617156G= , CM000673.2:g.6617156G=	GRCh38
NC_000011.9:g.6638387G= , CM000673.1:g.6638387G=	GRCh37
NC_000011.8:g.6594963G=	NCBI36
NG_008653.1:g.7306C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-3C=	ENSP00000507321.1:n.395-3C=
ENST00000299427.12:c.509-3C= MANE Select	ENSP00000299427.6:n.509-3C=
ENST00000428886.7:n.741C=
ENST00000436873.7:c.312+145C=
ENST00000524788.2:n.1665C=
ENST00000524903.2:n.1781C=
ENST00000528807.2:n.165-3C=
ENST00000530040.2:n.479+203C=
ENST00000533371.6:c.-221-3C=	ENSP00000437066.1:n.-221-3C=
ENST00000534644.6:n.457-3C=
ENST00000642892.1:c.-221-3C=	ENSP00000494165.1:n.-221-3C=
ENST00000643439.1:c.*249-3C=	ENSP00000495849.1:n.*249-3C=
ENST00000643479.1:n.538-3C=
ENST00000643516.1:c.395+145C=
ENST00000644151.1:n.1945C=
ENST00000644218.1:c.509-3C=	ENSP00000493574.1:n.509-3C=
ENST00000644683.1:c.451-3C=	ENSP00000494085.1:n.451-3C=
ENST00000644810.1:c.230-3C=	ENSP00000495895.1:n.230-3C=
ENST00000644831.1:n.682C=
ENST00000644933.1:c.-221-3C=	ENSP00000496133.1:n.-221-3C=
ENST00000645020.1:n.1681C=
ENST00000645285.1:c.-221-3C=	ENSP00000495058.1:n.-221-3C=
ENST00000645331.1:n.872C=
ENST00000645620.1:c.-221-3C=	ENSP00000493657.1:n.-221-3C=
ENST00000646777.1:n.682C=
ENST00000647016.1:n.986C=
ENST00000647152.1:c.-221-3C=	ENSP00000495893.1:n.-221-3C=
ENST00000647209.1:c.*378-3C=	ENSP00000495558.1:n.*378-3C=
ENST00000647346.1:n.1529-3C=
ENST00000299427.10:c.509-3C=	ENSP00000299427.6:n.509-3C=
ENST00000428886.6:n.675C=
ENST00000436873.6:c.450+203C=	ENSP00000398136.2:n.450+203C=
ENST00000524788.1:n.206C=
ENST00000528571.5:c.*249-3C=	ENSP00000434647.1:n.*249-3C=
ENST00000528807.1:n.56C=
ENST00000533371.5:c.-221-3C=	ENSP00000437066.1:n.-221-3C=
ENST00000534644.5:n.494-3C=
ENST00000611494.4:c.509-3C=	ENSP00000484546.1:n.509-3C=
NM_000391.3:c.509-3C=	NP_000382.3:n.509-3C=
NM_000391.4:c.509-3C= MANE Select	NP_000382.3:n.509-3C=