Canonical Allele Identifier: CA1950236681

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616472C= , CM000673.2:g.6616472C=	GRCh38
NC_000011.9:g.6637703C= , CM000673.1:g.6637703C=	GRCh37
NC_000011.8:g.6594279C=	NCBI36
NG_008653.1:g.7990G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.804G=	ENSP00000507321.1:p.Gln268=
ENST00000299427.12:c.918G= MANE Select	ENSP00000299427.6:p.Gln306=
ENST00000436873.7:c.313-398G=
ENST00000530040.2:n.511G=
ENST00000533371.6:c.189G=	ENSP00000437066.1:p.Gln63=
ENST00000642892.1:c.189G=	ENSP00000494165.1:p.Gln63=
ENST00000643342.1:c.8G=
ENST00000643439.1:c.*658G=	ENSP00000495849.1:n.*658G=
ENST00000643479.1:n.1104G=
ENST00000643516.1:c.427G=
ENST00000644218.1:c.886+189G=	ENSP00000493574.1:n.886+189G=
ENST00000644683.1:c.*371G=	ENSP00000494085.1:n.*371G=
ENST00000644810.1:c.639G=	ENSP00000495895.1:p.Gln213=
ENST00000644831.1:n.1094G=
ENST00000644933.1:c.189G=	ENSP00000496133.1:p.Gln63=
ENST00000645285.1:c.157+189G=	ENSP00000495058.1:n.157+189G=
ENST00000645331.1:n.1441G=
ENST00000645620.1:c.189G=	ENSP00000493657.1:p.Gln63=
ENST00000646691.1:n.11G=
ENST00000646777.1:n.1251G=
ENST00000647016.1:n.1398G=
ENST00000647152.1:c.189G=	ENSP00000495893.1:p.Gln63=
ENST00000647209.1:c.*787G=	ENSP00000495558.1:n.*787G=
ENST00000647346.1:n.1938G=
ENST00000299427.10:c.918G=	ENSP00000299427.6:p.Gln306=
ENST00000436873.6:c.482G=	ENSP00000398136.2:p.Ser161=
ENST00000533371.5:c.189G=	ENSP00000437066.1:p.Gln63=
ENST00000611494.4:c.918G=	ENSP00000484546.1:p.Gln306=
NM_000391.3:c.918G=	NP_000382.3:p.Gln306=
NM_000391.4:c.918G= MANE Select	NP_000382.3:p.Gln306=