Canonical Allele Identifier: CA1950235768

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616073A= , CM000673.2:g.6616073A=	GRCh38
NC_000011.9:g.6637304A= , CM000673.1:g.6637304A=	GRCh37
NC_000011.8:g.6593880A=	NCBI36
NG_008653.1:g.8389T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.963T=	ENSP00000507321.1:p.Gly321=
ENST00000299427.12:c.1077T= MANE Select	ENSP00000299427.6:p.Gly359=
ENST00000436873.7:c.314T=
ENST00000524924.2:n.197T=
ENST00000533371.6:c.348T=	ENSP00000437066.1:p.Gly116=
ENST00000642892.1:c.348T=	ENSP00000494165.1:p.Gly116=
ENST00000643342.1:c.167T=
ENST00000643439.1:c.*817T=	ENSP00000495849.1:n.*817T=
ENST00000643479.1:n.1263T=
ENST00000643516.1:c.586T=
ENST00000644218.1:c.888T=	ENSP00000493574.1:p.Gly296=
ENST00000644683.1:c.*530T=	ENSP00000494085.1:n.*530T=
ENST00000644810.1:c.798T=	ENSP00000495895.1:p.Gly266=
ENST00000644831.1:n.1253T=
ENST00000644933.1:c.348T=	ENSP00000496133.1:p.Gly116=
ENST00000645285.1:c.159T=	ENSP00000495058.1:p.Gly53=
ENST00000645331.1:n.1840T=
ENST00000645620.1:c.348T=	ENSP00000493657.1:p.Gly116=
ENST00000646691.1:n.410T=
ENST00000646777.1:n.1410T=
ENST00000647016.1:n.1557T=
ENST00000647152.1:c.348T=	ENSP00000495893.1:p.Gly116=
ENST00000647209.1:c.*946T=	ENSP00000495558.1:n.*946T=
ENST00000647346.1:n.2097T=
ENST00000299427.10:c.1077T=	ENSP00000299427.6:p.Gly359=
ENST00000524924.1:n.32T=
ENST00000533371.5:c.348T=	ENSP00000437066.1:p.Gly116=
ENST00000611494.4:c.1077T=	ENSP00000484546.1:p.Gly359=
NM_000391.3:c.1077T=	NP_000382.3:p.Gly359=
NM_000391.4:c.1077T= MANE Select	NP_000382.3:p.Gly359=