Canonical Allele Identifier: CA1950236261

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616325G= , CM000673.2:g.6616325G=	GRCh38
NC_000011.9:g.6637556G= , CM000673.1:g.6637556G=	GRCh37
NC_000011.8:g.6594132G=	NCBI36
NG_008653.1:g.8137C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.951C=	ENSP00000507321.1:p.Leu317=
ENST00000299427.12:c.1065C= MANE Select	ENSP00000299427.6:p.Leu355=
ENST00000436873.7:c.313-251C=
ENST00000533371.6:c.336C=	ENSP00000437066.1:p.Leu112=
ENST00000642892.1:c.336C=	ENSP00000494165.1:p.Leu112=
ENST00000643342.1:c.155C=
ENST00000643439.1:c.*805C=	ENSP00000495849.1:n.*805C=
ENST00000643479.1:n.1251C=
ENST00000643516.1:c.574C=
ENST00000644218.1:c.887-251C=	ENSP00000493574.1:n.887-251C=
ENST00000644683.1:c.*518C=	ENSP00000494085.1:n.*518C=
ENST00000644810.1:c.786C=	ENSP00000495895.1:p.Leu262=
ENST00000644831.1:n.1241C=
ENST00000644933.1:c.336C=	ENSP00000496133.1:p.Leu112=
ENST00000645285.1:c.158-251C=	ENSP00000495058.1:n.158-251C=
ENST00000645331.1:n.1588C=
ENST00000645620.1:c.336C=	ENSP00000493657.1:p.Leu112=
ENST00000646691.1:n.158C=
ENST00000646777.1:n.1398C=
ENST00000647016.1:n.1545C=
ENST00000647152.1:c.336C=	ENSP00000495893.1:p.Leu112=
ENST00000647209.1:c.*934C=	ENSP00000495558.1:n.*934C=
ENST00000647346.1:n.2085C=
ENST00000299427.10:c.1065C=	ENSP00000299427.6:p.Leu355=
ENST00000533371.5:c.336C=	ENSP00000437066.1:p.Leu112=
ENST00000611494.4:c.1065C=	ENSP00000484546.1:p.Leu355=
NM_000391.3:c.1065C=	NP_000382.3:p.Leu355=
NM_000391.4:c.1065C= MANE Select	NP_000382.3:p.Leu355=