Canonical Allele Identifier: CA1950236838

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616508A= , CM000673.2:g.6616508A=	GRCh38
NC_000011.9:g.6637739A= , CM000673.1:g.6637739A=	GRCh37
NC_000011.8:g.6594315A=	NCBI36
NG_008653.1:g.7954T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.773-5T=	ENSP00000507321.1:n.773-5T=
ENST00000299427.12:c.887-5T= MANE Select	ENSP00000299427.6:n.887-5T=
ENST00000436873.7:c.313-434T=
ENST00000530040.2:n.480-5T=
ENST00000533371.6:c.158-5T=	ENSP00000437066.1:n.158-5T=
ENST00000642892.1:c.158-5T=	ENSP00000494165.1:n.158-5T=
ENST00000643439.1:c.*627-5T=	ENSP00000495849.1:n.*627-5T=
ENST00000643479.1:n.1068T=
ENST00000643516.1:c.396-5T=
ENST00000644218.1:c.886+153T=	ENSP00000493574.1:n.886+153T=
ENST00000644683.1:c.*340-5T=	ENSP00000494085.1:n.*340-5T=
ENST00000644810.1:c.608-5T=	ENSP00000495895.1:n.608-5T=
ENST00000644831.1:n.1063-5T=
ENST00000644933.1:c.158-5T=	ENSP00000496133.1:n.158-5T=
ENST00000645285.1:c.157+153T=	ENSP00000495058.1:n.157+153T=
ENST00000645331.1:n.1405T=
ENST00000645620.1:c.158-5T=	ENSP00000493657.1:n.158-5T=
ENST00000646777.1:n.1215T=
ENST00000647016.1:n.1367-5T=
ENST00000647152.1:c.158-5T=	ENSP00000495893.1:n.158-5T=
ENST00000647209.1:c.*756-5T=	ENSP00000495558.1:n.*756-5T=
ENST00000647346.1:n.1907-5T=
ENST00000299427.10:c.887-5T=	ENSP00000299427.6:n.887-5T=
ENST00000436873.6:c.451-5T=	ENSP00000398136.2:n.451-5T=
ENST00000533371.5:c.158-5T=	ENSP00000437066.1:n.158-5T=
ENST00000611494.4:c.887-5T=	ENSP00000484546.1:n.887-5T=
NM_000391.3:c.887-5T=	NP_000382.3:n.887-5T=
NM_000391.4:c.887-5T= MANE Select	NP_000382.3:n.887-5T=