Canonical Allele Identifier: CA1950236959

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616547T= , CM000673.2:g.6616547T=	GRCh38
NC_000011.9:g.6637778T= , CM000673.1:g.6637778T=	GRCh37
NC_000011.8:g.6594354T=	NCBI36
NG_008653.1:g.7915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-44A=	ENSP00000507321.1:n.773-44A=
ENST00000299427.12:c.887-44A= MANE Select	ENSP00000299427.6:n.887-44A=
ENST00000436873.7:c.313-473A=
ENST00000524903.2:n.2275A=
ENST00000528807.2:n.656A=
ENST00000530040.2:n.480-44A=
ENST00000533371.6:c.158-44A=	ENSP00000437066.1:n.158-44A=
ENST00000642892.1:c.158-44A=	ENSP00000494165.1:n.158-44A=
ENST00000643439.1:c.*627-44A=	ENSP00000495849.1:n.*627-44A=
ENST00000643479.1:n.1029A=
ENST00000643516.1:c.396-44A=
ENST00000644218.1:c.886+114A=	ENSP00000493574.1:n.886+114A=
ENST00000644683.1:c.*340-44A=	ENSP00000494085.1:n.*340-44A=
ENST00000644810.1:c.608-44A=	ENSP00000495895.1:n.608-44A=
ENST00000644831.1:n.1063-44A=
ENST00000644933.1:c.158-44A=	ENSP00000496133.1:n.158-44A=
ENST00000645020.1:n.2290A=
ENST00000645285.1:c.157+114A=	ENSP00000495058.1:n.157+114A=
ENST00000645331.1:n.1366A=
ENST00000645620.1:c.158-44A=	ENSP00000493657.1:n.158-44A=
ENST00000646777.1:n.1176A=
ENST00000647016.1:n.1367-44A=
ENST00000647152.1:c.158-44A=	ENSP00000495893.1:n.158-44A=
ENST00000647209.1:c.*756-44A=	ENSP00000495558.1:n.*756-44A=
ENST00000647346.1:n.1907-44A=
ENST00000299427.10:c.887-44A=	ENSP00000299427.6:n.887-44A=
ENST00000436873.6:c.451-44A=	ENSP00000398136.2:n.451-44A=
ENST00000528807.1:n.550A=
ENST00000533371.5:c.158-44A=	ENSP00000437066.1:n.158-44A=
ENST00000611494.4:c.887-44A=	ENSP00000484546.1:n.887-44A=
NM_000391.3:c.887-44A=	NP_000382.3:n.887-44A=
NM_000391.4:c.887-44A= MANE Select	NP_000382.3:n.887-44A=