Canonical Allele Identifier: CA379472509

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636403G>T (hg19) ; chr11:g.6615172G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615172G>T , CM000673.2:g.6615172G>T	GRCh38
NC_000011.9:g.6636403G>T , CM000673.1:g.6636403G>T	GRCh37
NC_000011.8:g.6592979G>T	NCBI36
NG_008653.1:g.9290C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1310C>A	ENSP00000507321.1:p.Ser437Ter
ENST00000299427.12:c.1424C>A MANE Select	ENSP00000299427.6:p.Ser475Ter
ENST00000524611.2:n.284C>A
ENST00000524924.2:n.544C>A
ENST00000533371.6:c.695C>A	ENSP00000437066.1:p.Ser232Ter
ENST00000642892.1:c.695C>A	ENSP00000494165.1:p.Ser232Ter
ENST00000643342.1:c.497C>A
ENST00000643439.1:c.*1164C>A	ENSP00000495849.1:n.*1164C>A
ENST00000643479.1:n.1610C>A
ENST00000643516.1:c.933C>A
ENST00000644218.1:c.1235C>A	ENSP00000493574.1:p.Ser412Ter
ENST00000644683.1:c.*877C>A	ENSP00000494085.1:n.*877C>A
ENST00000644810.1:c.1145C>A	ENSP00000495895.1:p.Ser382Ter
ENST00000644831.1:n.1600C>A
ENST00000644933.1:c.*290C>A	ENSP00000496133.1:n.*290C>A
ENST00000645285.1:c.*290C>A	ENSP00000495058.1:n.*290C>A
ENST00000645331.1:n.2629C>A
ENST00000645620.1:c.695C>A	ENSP00000493657.1:p.Ser232Ter
ENST00000646691.1:n.1311C>A
ENST00000646777.1:n.1757C>A
ENST00000647016.1:n.1904C>A
ENST00000647152.1:c.695C>A	ENSP00000495893.1:p.Ser232Ter
ENST00000647209.1:c.*1293C>A	ENSP00000495558.1:n.*1293C>A
ENST00000647346.1:n.2444C>A
ENST00000299427.10:c.1424C>A	ENSP00000299427.6:p.Ser475Ter
ENST00000524611.1:n.302C>A
ENST00000533371.5:c.695C>A	ENSP00000437066.1:p.Ser232Ter
ENST00000611494.4:c.1424C>A	ENSP00000484546.1:p.Ser475Ter
NM_000391.3:c.1424C>A	NP_000382.3:p.Ser475Ter
NM_000391.4:c.1424C>A MANE Select	NP_000382.3:p.Ser475Ter