Canonical Allele Identifier: CA1950236983

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616559G= , CM000673.2:g.6616559G=	GRCh38
NC_000011.9:g.6637790G= , CM000673.1:g.6637790G=	GRCh37
NC_000011.8:g.6594366G=	NCBI36
NG_008653.1:g.7903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-56C=	ENSP00000507321.1:n.773-56C=
ENST00000299427.12:c.887-56C= MANE Select	ENSP00000299427.6:n.887-56C=
ENST00000436873.7:c.313-485C=
ENST00000524903.2:n.2263C=
ENST00000528807.2:n.644C=
ENST00000530040.2:n.480-56C=
ENST00000533371.6:c.158-56C=	ENSP00000437066.1:n.158-56C=
ENST00000642892.1:c.158-56C=	ENSP00000494165.1:n.158-56C=
ENST00000643439.1:c.*627-56C=	ENSP00000495849.1:n.*627-56C=
ENST00000643479.1:n.1017C=
ENST00000643516.1:c.396-56C=
ENST00000644218.1:c.886+102C=	ENSP00000493574.1:n.886+102C=
ENST00000644683.1:c.*340-56C=	ENSP00000494085.1:n.*340-56C=
ENST00000644810.1:c.608-56C=	ENSP00000495895.1:n.608-56C=
ENST00000644831.1:n.1063-56C=
ENST00000644933.1:c.158-56C=	ENSP00000496133.1:n.158-56C=
ENST00000645020.1:n.2278C=
ENST00000645285.1:c.157+102C=	ENSP00000495058.1:n.157+102C=
ENST00000645331.1:n.1354C=
ENST00000645620.1:c.158-56C=	ENSP00000493657.1:n.158-56C=
ENST00000646777.1:n.1164C=
ENST00000647016.1:n.1367-56C=
ENST00000647152.1:c.158-56C=	ENSP00000495893.1:n.158-56C=
ENST00000647209.1:c.*756-56C=	ENSP00000495558.1:n.*756-56C=
ENST00000647346.1:n.1907-56C=
ENST00000299427.10:c.887-56C=	ENSP00000299427.6:n.887-56C=
ENST00000436873.6:c.451-56C=	ENSP00000398136.2:n.451-56C=
ENST00000528807.1:n.538C=
ENST00000533371.5:c.158-56C=	ENSP00000437066.1:n.158-56C=
ENST00000611494.4:c.887-56C=	ENSP00000484546.1:n.887-56C=
NM_000391.3:c.887-56C=	NP_000382.3:n.887-56C=
NM_000391.4:c.887-56C= MANE Select	NP_000382.3:n.887-56C=