Canonical Allele Identifier: CA1950232490

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614507C= , CM000673.2:g.6614507C=	GRCh38
NC_000011.9:g.6635738C= , CM000673.1:g.6635738C=	GRCh37
NC_000011.8:g.6592314C=	NCBI36
NG_008653.1:g.9955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*39G=	ENSP00000507321.1:n.*39G=
ENST00000299427.12:c.*39G= MANE Select	ENSP00000299427.6:n.*39G=
ENST00000524611.2:n.770G=
ENST00000533371.6:c.*39G=	ENSP00000437066.1:n.*39G=
ENST00000642892.1:c.*39G=	ENSP00000494165.1:n.*39G=
ENST00000643342.1:c.804G=
ENST00000643439.1:c.*1471G=	ENSP00000495849.1:n.*1471G=
ENST00000643479.1:n.1917G=
ENST00000643516.1:c.1240G=
ENST00000644218.1:c.*39G=	ENSP00000493574.1:n.*39G=
ENST00000644683.1:c.*1184G=	ENSP00000494085.1:n.*1184G=
ENST00000644810.1:c.*39G=	ENSP00000495895.1:n.*39G=
ENST00000644831.1:n.1907G=
ENST00000644933.1:c.*597G=	ENSP00000496133.1:n.*597G=
ENST00000645285.1:c.*597G=	ENSP00000495058.1:n.*597G=
ENST00000645331.1:n.2936G=
ENST00000645620.1:c.*39G=	ENSP00000493657.1:n.*39G=
ENST00000646691.1:n.1618G=
ENST00000646777.1:n.2064G=
ENST00000647016.1:n.2211G=
ENST00000647152.1:c.*39G=	ENSP00000495893.1:n.*39G=
ENST00000647209.1:c.*1600G=	ENSP00000495558.1:n.*1600G=
ENST00000647346.1:n.2751G=
ENST00000299427.10:c.*39G=	ENSP00000299427.6:n.*39G=
ENST00000533371.5:c.*39G=	ENSP00000437066.1:n.*39G=
ENST00000611494.4:c.*59G=	ENSP00000484546.1:n.*59G=
NM_000391.3:c.*39G=	NP_000382.3:n.*39G=
NM_000391.4:c.*39G= MANE Select	NP_000382.3:n.*39G=