Canonical Allele Identifier: CA1950232608

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614578G= , CM000673.2:g.6614578G=	GRCh38
NC_000011.9:g.6635809G= , CM000673.1:g.6635809G=	GRCh37
NC_000011.8:g.6592385G=	NCBI36
NG_008653.1:g.9884C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1546C=	ENSP00000507321.1:p.Pro516=
ENST00000299427.12:c.1660C= MANE Select	ENSP00000299427.6:p.Pro554=
ENST00000524611.2:n.699C=
ENST00000533371.6:c.931C=	ENSP00000437066.1:p.Pro311=
ENST00000642892.1:c.931C=	ENSP00000494165.1:p.Pro311=
ENST00000643342.1:c.733C=
ENST00000643439.1:c.*1400C=	ENSP00000495849.1:n.*1400C=
ENST00000643479.1:n.1846C=
ENST00000643516.1:c.1169C=
ENST00000644218.1:c.1471C=	ENSP00000493574.1:p.Pro491=
ENST00000644683.1:c.*1113C=	ENSP00000494085.1:n.*1113C=
ENST00000644810.1:c.1381C=	ENSP00000495895.1:p.Pro461=
ENST00000644831.1:n.1836C=
ENST00000644933.1:c.*526C=	ENSP00000496133.1:n.*526C=
ENST00000645285.1:c.*526C=	ENSP00000495058.1:n.*526C=
ENST00000645331.1:n.2865C=
ENST00000645620.1:c.931C=	ENSP00000493657.1:p.Pro311=
ENST00000646691.1:n.1547C=
ENST00000646777.1:n.1993C=
ENST00000647016.1:n.2140C=
ENST00000647152.1:c.931C=	ENSP00000495893.1:p.Pro311=
ENST00000647209.1:c.*1529C=	ENSP00000495558.1:n.*1529C=
ENST00000647346.1:n.2680C=
ENST00000299427.10:c.1660C=	ENSP00000299427.6:p.Pro554=
ENST00000533371.5:c.931C=	ENSP00000437066.1:p.Pro311=
ENST00000611494.4:c.1659C=	ENSP00000484546.1:p.Ser553=
NM_000391.3:c.1660C=	NP_000382.3:p.Pro554=
NM_000391.4:c.1660C= MANE Select	NP_000382.3:p.Pro554=