Canonical Allele Identifier: CA1950234430

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615397C= , CM000673.2:g.6615397C=	GRCh38
NC_000011.9:g.6636628C= , CM000673.1:g.6636628C=	GRCh37
NC_000011.8:g.6593204C=	NCBI36
NG_008653.1:g.9065G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1152+45G=	ENSP00000507321.1:n.1152+45G=
ENST00000299427.12:c.1266+45G= MANE Select	ENSP00000299427.6:n.1266+45G=
ENST00000436873.7:c.503+45G=
ENST00000524611.2:n.59G=
ENST00000524924.2:n.386+45G=
ENST00000533371.6:c.537+45G=	ENSP00000437066.1:n.537+45G=
ENST00000642892.1:c.537+45G=	ENSP00000494165.1:n.537+45G=
ENST00000643342.1:c.339+45G=
ENST00000643439.1:c.*1006+45G=	ENSP00000495849.1:n.*1006+45G=
ENST00000643479.1:n.1452+45G=
ENST00000643516.1:c.775+45G=
ENST00000644218.1:c.1077+45G=	ENSP00000493574.1:n.1077+45G=
ENST00000644683.1:c.*719+45G=	ENSP00000494085.1:n.*719+45G=
ENST00000644810.1:c.987+45G=	ENSP00000495895.1:n.987+45G=
ENST00000644831.1:n.1442+45G=
ENST00000644933.1:c.*132+45G=	ENSP00000496133.1:n.*132+45G=
ENST00000645285.1:c.*132+45G=	ENSP00000495058.1:n.*132+45G=
ENST00000645331.1:n.2471+45G=
ENST00000645620.1:c.537+45G=	ENSP00000493657.1:n.537+45G=
ENST00000646691.1:n.1086G=
ENST00000646777.1:n.1599+45G=
ENST00000647016.1:n.1746+45G=
ENST00000647152.1:c.537+45G=	ENSP00000495893.1:n.537+45G=
ENST00000647209.1:c.*1135+45G=	ENSP00000495558.1:n.*1135+45G=
ENST00000647346.1:n.2286+45G=
ENST00000299427.10:c.1266+45G=	ENSP00000299427.6:n.1266+45G=
ENST00000524611.1:n.77G=
ENST00000524924.1:n.221+45G=
ENST00000532191.1:n.319+45G=
ENST00000533371.5:c.537+45G=	ENSP00000437066.1:n.537+45G=
ENST00000611494.4:c.1266+45G=	ENSP00000484546.1:n.1266+45G=
NM_000391.3:c.1266+45G=	NP_000382.3:n.1266+45G=
NM_000391.4:c.1266+45G= MANE Select	NP_000382.3:n.1266+45G=