Canonical Allele Identifier: CA1950234750

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615542C= , CM000673.2:g.6615542C=	GRCh38
NC_000011.9:g.6636773C= , CM000673.1:g.6636773C=	GRCh37
NC_000011.8:g.6593349C=	NCBI36
NG_008653.1:g.8920G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1052G=	ENSP00000507321.1:p.Gly351=
ENST00000299427.12:c.1166G= MANE Select	ENSP00000299427.6:p.Gly389=
ENST00000436873.7:c.403G=
ENST00000524924.2:n.286G=
ENST00000533371.6:c.437G=	ENSP00000437066.1:p.Gly146=
ENST00000642892.1:c.437G=	ENSP00000494165.1:p.Gly146=
ENST00000643342.1:c.239G=
ENST00000643439.1:c.*906G=	ENSP00000495849.1:n.*906G=
ENST00000643479.1:n.1352G=
ENST00000643516.1:c.675G=
ENST00000644218.1:c.977G=	ENSP00000493574.1:p.Gly326=
ENST00000644683.1:c.*619G=	ENSP00000494085.1:n.*619G=
ENST00000644810.1:c.887G=	ENSP00000495895.1:p.Gly296=
ENST00000644831.1:n.1342G=
ENST00000644933.1:c.*32G=	ENSP00000496133.1:n.*32G=
ENST00000645285.1:c.*32G=	ENSP00000495058.1:n.*32G=
ENST00000645331.1:n.2371G=
ENST00000645620.1:c.437G=	ENSP00000493657.1:p.Gly146=
ENST00000646691.1:n.941G=
ENST00000646777.1:n.1499G=
ENST00000647016.1:n.1646G=
ENST00000647152.1:c.437G=	ENSP00000495893.1:p.Gly146=
ENST00000647209.1:c.*1035G=	ENSP00000495558.1:n.*1035G=
ENST00000647346.1:n.2186G=
ENST00000299427.10:c.1166G=	ENSP00000299427.6:p.Gly389=
ENST00000524924.1:n.121G=
ENST00000532191.1:n.219G=
ENST00000533371.5:c.437G=	ENSP00000437066.1:p.Gly146=
ENST00000611494.4:c.1166G=	ENSP00000484546.1:p.Gly389=
NM_000391.3:c.1166G=	NP_000382.3:p.Gly389=
NM_000391.4:c.1166G= MANE Select	NP_000382.3:p.Gly389=