Canonical Allele Identifier: CA472922302

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636489G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615258G>T , CM000673.2:g.6615258G>T	GRCh38
NC_000011.9:g.6636489G>T , CM000673.1:g.6636489G>T	GRCh37
NC_000011.8:g.6593065G>T	NCBI36
NG_008653.1:g.9204C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1224C>A	ENSP00000507321.1:p.Gly408=
ENST00000299427.12:c.1338C>A MANE Select	ENSP00000299427.6:p.Gly446=
ENST00000524611.2:n.198C>A
ENST00000524924.2:n.458C>A
ENST00000533371.6:c.609C>A	ENSP00000437066.1:p.Gly203=
ENST00000642892.1:c.609C>A	ENSP00000494165.1:p.Gly203=
ENST00000643342.1:c.411C>A
ENST00000643439.1:c.*1078C>A	ENSP00000495849.1:n.*1078C>A
ENST00000643479.1:n.1524C>A
ENST00000643516.1:c.847C>A
ENST00000644218.1:c.1149C>A	ENSP00000493574.1:p.Gly383=
ENST00000644683.1:c.*791C>A	ENSP00000494085.1:n.*791C>A
ENST00000644810.1:c.1059C>A	ENSP00000495895.1:p.Gly353=
ENST00000644831.1:n.1514C>A
ENST00000644933.1:c.*204C>A	ENSP00000496133.1:n.*204C>A
ENST00000645285.1:c.*204C>A	ENSP00000495058.1:n.*204C>A
ENST00000645331.1:n.2543C>A
ENST00000645620.1:c.609C>A	ENSP00000493657.1:p.Gly203=
ENST00000646691.1:n.1225C>A
ENST00000646777.1:n.1671C>A
ENST00000647016.1:n.1818C>A
ENST00000647152.1:c.609C>A	ENSP00000495893.1:p.Gly203=
ENST00000647209.1:c.*1207C>A	ENSP00000495558.1:n.*1207C>A
ENST00000647346.1:n.2358C>A
ENST00000299427.10:c.1338C>A	ENSP00000299427.6:p.Gly446=
ENST00000524611.1:n.216C>A
ENST00000532191.1:n.391C>A
ENST00000533371.5:c.609C>A	ENSP00000437066.1:p.Gly203=
ENST00000611494.4:c.1338C>A	ENSP00000484546.1:p.Gly446=
NM_000391.3:c.1338C>A	NP_000382.3:p.Gly446=
NM_000391.4:c.1338C>A MANE Select	NP_000382.3:p.Gly446=