Canonical Allele Identifier: CA1950234460

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615413C= , CM000673.2:g.6615413C=	GRCh38
NC_000011.9:g.6636644C= , CM000673.1:g.6636644C=	GRCh37
NC_000011.8:g.6593220C=	NCBI36
NG_008653.1:g.9049G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1152+29G=	ENSP00000507321.1:n.1152+29G=
ENST00000299427.12:c.1266+29G= MANE Select	ENSP00000299427.6:n.1266+29G=
ENST00000436873.7:c.503+29G=
ENST00000524611.2:n.43G=
ENST00000524924.2:n.386+29G=
ENST00000533371.6:c.537+29G=	ENSP00000437066.1:n.537+29G=
ENST00000642892.1:c.537+29G=	ENSP00000494165.1:n.537+29G=
ENST00000643342.1:c.339+29G=
ENST00000643439.1:c.*1006+29G=	ENSP00000495849.1:n.*1006+29G=
ENST00000643479.1:n.1452+29G=
ENST00000643516.1:c.775+29G=
ENST00000644218.1:c.1077+29G=	ENSP00000493574.1:n.1077+29G=
ENST00000644683.1:c.*719+29G=	ENSP00000494085.1:n.*719+29G=
ENST00000644810.1:c.987+29G=	ENSP00000495895.1:n.987+29G=
ENST00000644831.1:n.1442+29G=
ENST00000644933.1:c.*132+29G=	ENSP00000496133.1:n.*132+29G=
ENST00000645285.1:c.*132+29G=	ENSP00000495058.1:n.*132+29G=
ENST00000645331.1:n.2471+29G=
ENST00000645620.1:c.537+29G=	ENSP00000493657.1:n.537+29G=
ENST00000646691.1:n.1070G=
ENST00000646777.1:n.1599+29G=
ENST00000647016.1:n.1746+29G=
ENST00000647152.1:c.537+29G=	ENSP00000495893.1:n.537+29G=
ENST00000647209.1:c.*1135+29G=	ENSP00000495558.1:n.*1135+29G=
ENST00000647346.1:n.2286+29G=
ENST00000299427.10:c.1266+29G=	ENSP00000299427.6:n.1266+29G=
ENST00000524611.1:n.61G=
ENST00000524924.1:n.221+29G=
ENST00000532191.1:n.319+29G=
ENST00000533371.5:c.537+29G=	ENSP00000437066.1:n.537+29G=
ENST00000611494.4:c.1266+29G=	ENSP00000484546.1:n.1266+29G=
NM_000391.3:c.1266+29G=	NP_000382.3:n.1266+29G=
NM_000391.4:c.1266+29G= MANE Select	NP_000382.3:n.1266+29G=