Canonical Allele Identifier: CA1950237058

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616630C= , CM000673.2:g.6616630C=	GRCh38
NC_000011.9:g.6637861C= , CM000673.1:g.6637861C=	GRCh37
NC_000011.8:g.6594437C=	NCBI36
NG_008653.1:g.7832G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.772+31G=	ENSP00000507321.1:n.772+31G=
ENST00000299427.12:c.886+31G= MANE Select	ENSP00000299427.6:n.886+31G=
ENST00000436873.7:c.313-556G=
ENST00000524788.2:n.2076G=
ENST00000524903.2:n.2192G=
ENST00000528807.2:n.573G=
ENST00000530040.2:n.480-127G=
ENST00000533371.6:c.157+31G=	ENSP00000437066.1:n.157+31G=
ENST00000642892.1:c.157+31G=	ENSP00000494165.1:n.157+31G=
ENST00000643439.1:c.*626+31G=	ENSP00000495849.1:n.*626+31G=
ENST00000643479.1:n.946G=
ENST00000643516.1:c.396-127G=
ENST00000644218.1:c.886+31G=	ENSP00000493574.1:n.886+31G=
ENST00000644683.1:c.*339+31G=	ENSP00000494085.1:n.*339+31G=
ENST00000644810.1:c.607+31G=	ENSP00000495895.1:n.607+31G=
ENST00000644831.1:n.1062+31G=
ENST00000644933.1:c.157+31G=	ENSP00000496133.1:n.157+31G=
ENST00000645020.1:n.2207G=
ENST00000645285.1:c.157+31G=	ENSP00000495058.1:n.157+31G=
ENST00000645331.1:n.1283G=
ENST00000645620.1:c.157+31G=	ENSP00000493657.1:n.157+31G=
ENST00000646777.1:n.1093G=
ENST00000647016.1:n.1366+31G=
ENST00000647152.1:c.157+31G=	ENSP00000495893.1:n.157+31G=
ENST00000647209.1:c.*755+31G=	ENSP00000495558.1:n.*755+31G=
ENST00000647346.1:n.1906+31G=
ENST00000299427.10:c.886+31G=	ENSP00000299427.6:n.886+31G=
ENST00000436873.6:c.451-127G=	ENSP00000398136.2:n.451-127G=
ENST00000528807.1:n.467G=
ENST00000533371.5:c.157+31G=	ENSP00000437066.1:n.157+31G=
ENST00000611494.4:c.886+31G=	ENSP00000484546.1:n.886+31G=
NM_000391.3:c.886+31G=	NP_000382.3:n.886+31G=
NM_000391.4:c.886+31G= MANE Select	NP_000382.3:n.886+31G=