Canonical Allele Identifier: CA1950235726

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616064C= , CM000673.2:g.6616064C=	GRCh38
NC_000011.9:g.6637295C= , CM000673.1:g.6637295C=	GRCh37
NC_000011.8:g.6593871C=	NCBI36
NG_008653.1:g.8398G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.972G=	ENSP00000507321.1:p.Gly324=
ENST00000299427.12:c.1086G= MANE Select	ENSP00000299427.6:p.Gly362=
ENST00000436873.7:c.323G=
ENST00000524924.2:n.206G=
ENST00000533371.6:c.357G=	ENSP00000437066.1:p.Gly119=
ENST00000642892.1:c.357G=	ENSP00000494165.1:p.Gly119=
ENST00000643342.1:c.176G=
ENST00000643439.1:c.*826G=	ENSP00000495849.1:n.*826G=
ENST00000643479.1:n.1272G=
ENST00000643516.1:c.595G=
ENST00000644218.1:c.897G=	ENSP00000493574.1:p.Gly299=
ENST00000644683.1:c.*539G=	ENSP00000494085.1:n.*539G=
ENST00000644810.1:c.807G=	ENSP00000495895.1:p.Gly269=
ENST00000644831.1:n.1262G=
ENST00000644933.1:c.357G=	ENSP00000496133.1:p.Gly119=
ENST00000645285.1:c.168G=	ENSP00000495058.1:p.Gly56=
ENST00000645331.1:n.1849G=
ENST00000645620.1:c.357G=	ENSP00000493657.1:p.Gly119=
ENST00000646691.1:n.419G=
ENST00000646777.1:n.1419G=
ENST00000647016.1:n.1566G=
ENST00000647152.1:c.357G=	ENSP00000495893.1:p.Gly119=
ENST00000647209.1:c.*955G=	ENSP00000495558.1:n.*955G=
ENST00000647346.1:n.2106G=
ENST00000299427.10:c.1086G=	ENSP00000299427.6:p.Gly362=
ENST00000524924.1:n.41G=
ENST00000533371.5:c.357G=	ENSP00000437066.1:p.Gly119=
ENST00000611494.4:c.1086G=	ENSP00000484546.1:p.Gly362=
NM_000391.3:c.1086G=	NP_000382.3:p.Gly362=
NM_000391.4:c.1086G= MANE Select	NP_000382.3:p.Gly362=