Canonical Allele Identifier: CA1950235471

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615990G= , CM000673.2:g.6615990G=	GRCh38
NC_000011.9:g.6637221G= , CM000673.1:g.6637221G=	GRCh37
NC_000011.8:g.6593797G=	NCBI36
NG_008653.1:g.8472C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1031+15C=	ENSP00000507321.1:n.1031+15C=
ENST00000299427.12:c.1145+15C= MANE Select	ENSP00000299427.6:n.1145+15C=
ENST00000436873.7:c.382+15C=
ENST00000524924.2:n.265+15C=
ENST00000533371.6:c.416+15C=	ENSP00000437066.1:n.416+15C=
ENST00000642892.1:c.416+15C=	ENSP00000494165.1:n.416+15C=
ENST00000643342.1:c.235+15C=
ENST00000643439.1:c.*885+15C=	ENSP00000495849.1:n.*885+15C=
ENST00000643479.1:n.1331+15C=
ENST00000643516.1:c.654+15C=
ENST00000644218.1:c.956+15C=	ENSP00000493574.1:n.956+15C=
ENST00000644683.1:c.*598+15C=	ENSP00000494085.1:n.*598+15C=
ENST00000644810.1:c.866+15C=	ENSP00000495895.1:n.866+15C=
ENST00000644831.1:n.1321+15C=
ENST00000644933.1:c.416+15C=	ENSP00000496133.1:n.416+15C=
ENST00000645285.1:c.227+15C=	ENSP00000495058.1:n.227+15C=
ENST00000645331.1:n.1923C=
ENST00000645620.1:c.416+15C=	ENSP00000493657.1:n.416+15C=
ENST00000646691.1:n.493C=
ENST00000646777.1:n.1478+15C=
ENST00000647016.1:n.1625+15C=
ENST00000647152.1:c.416+15C=	ENSP00000495893.1:n.416+15C=
ENST00000647209.1:c.*1014+15C=	ENSP00000495558.1:n.*1014+15C=
ENST00000647346.1:n.2165+15C=
ENST00000299427.10:c.1145+15C=	ENSP00000299427.6:n.1145+15C=
ENST00000524924.1:n.100+15C=
ENST00000533371.5:c.416+15C=	ENSP00000437066.1:n.416+15C=
ENST00000611494.4:c.1145+15C=	ENSP00000484546.1:n.1145+15C=
NM_000391.3:c.1145+15C=	NP_000382.3:n.1145+15C=
NM_000391.4:c.1145+15C= MANE Select	NP_000382.3:n.1145+15C=