Canonical Allele Identifier: CA1950237100

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616664G= , CM000673.2:g.6616664G=	GRCh38
NC_000011.9:g.6637895G= , CM000673.1:g.6637895G=	GRCh37
NC_000011.8:g.6594471G=	NCBI36
NG_008653.1:g.7798C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.769C=	ENSP00000507321.1:p.Pro257=
ENST00000299427.12:c.883C= MANE Select	ENSP00000299427.6:p.Pro295=
ENST00000436873.7:c.313-590C=
ENST00000524788.2:n.2042C=
ENST00000524903.2:n.2158C=
ENST00000528807.2:n.539C=
ENST00000530040.2:n.480-161C=
ENST00000533371.6:c.154C=	ENSP00000437066.1:p.Pro52=
ENST00000642892.1:c.154C=	ENSP00000494165.1:p.Pro52=
ENST00000643439.1:c.*623C=	ENSP00000495849.1:n.*623C=
ENST00000643479.1:n.912C=
ENST00000643516.1:c.396-161C=
ENST00000644151.1:n.2322C=
ENST00000644218.1:c.883C=	ENSP00000493574.1:p.Pro295=
ENST00000644683.1:c.*336C=	ENSP00000494085.1:n.*336C=
ENST00000644810.1:c.604C=	ENSP00000495895.1:p.Pro202=
ENST00000644831.1:n.1059C=
ENST00000644933.1:c.154C=	ENSP00000496133.1:p.Pro52=
ENST00000645020.1:n.2173C=
ENST00000645285.1:c.154C=	ENSP00000495058.1:p.Pro52=
ENST00000645331.1:n.1249C=
ENST00000645620.1:c.154C=	ENSP00000493657.1:p.Pro52=
ENST00000646777.1:n.1059C=
ENST00000647016.1:n.1363C=
ENST00000647152.1:c.154C=	ENSP00000495893.1:p.Pro52=
ENST00000647209.1:c.*752C=	ENSP00000495558.1:n.*752C=
ENST00000647346.1:n.1903C=
ENST00000299427.10:c.883C=	ENSP00000299427.6:p.Pro295=
ENST00000436873.6:c.451-161C=	ENSP00000398136.2:n.451-161C=
ENST00000528807.1:n.433C=
ENST00000533371.5:c.154C=	ENSP00000437066.1:p.Pro52=
ENST00000611494.4:c.883C=	ENSP00000484546.1:p.Pro295=
NM_000391.3:c.883C=	NP_000382.3:p.Pro295=
NM_000391.4:c.883C= MANE Select	NP_000382.3:p.Pro295=