Canonical Allele Identifier: CA217323994

Gene: TPP1

Linked Data

• dbSNP Id: rs769043106
• MyVariant Identifiers: chr11:g.6638618T>G (hg19) ; chr11:g.6617387T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617387T>G , CM000673.2:g.6617387T>G	GRCh38
NC_000011.9:g.6638618T>G , CM000673.1:g.6638618T>G	GRCh37
NC_000011.8:g.6595194T>G	NCBI36
NG_008653.1:g.7075A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.308A>C	ENSP00000507321.1:p.Tyr103Ser
ENST00000299427.12:c.422A>C MANE Select	ENSP00000299427.6:p.Tyr141Ser
ENST00000428886.7:n.510A>C
ENST00000436873.7:c.226A>C
ENST00000524788.2:n.1434A>C
ENST00000524903.2:n.1550A>C
ENST00000528571.6:c.*162A>C	ENSP00000434647.1:n.*162A>C
ENST00000528807.2:n.78A>C
ENST00000530040.2:n.451A>C
ENST00000533371.6:c.-308A>C	ENSP00000437066.1:n.-308A>C
ENST00000534644.6:n.423A>C
ENST00000642892.1:c.-255A>C	ENSP00000494165.1:n.-255A>C
ENST00000643439.1:c.*162A>C	ENSP00000495849.1:n.*162A>C
ENST00000643479.1:n.451A>C
ENST00000643516.1:c.309A>C
ENST00000644151.1:n.1714A>C
ENST00000644218.1:c.422A>C	ENSP00000493574.1:p.Tyr141Ser
ENST00000644683.1:c.422A>C	ENSP00000494085.1:p.Tyr141Ser
ENST00000644810.1:c.230-234A>C	ENSP00000495895.1:n.230-234A>C
ENST00000644831.1:n.451A>C
ENST00000644933.1:c.-308A>C	ENSP00000496133.1:n.-308A>C
ENST00000645020.1:n.1450A>C
ENST00000645285.1:c.-308A>C	ENSP00000495058.1:n.-308A>C
ENST00000645331.1:n.641A>C
ENST00000645620.1:c.-250A>C	ENSP00000493657.1:n.-250A>C
ENST00000646777.1:n.451A>C
ENST00000647016.1:n.755A>C
ENST00000647152.1:c.-308A>C	ENSP00000495893.1:n.-308A>C
ENST00000647209.1:c.*291A>C	ENSP00000495558.1:n.*291A>C
ENST00000647346.1:n.1442A>C
ENST00000299427.10:c.422A>C	ENSP00000299427.6:p.Tyr141Ser
ENST00000428886.6:n.444A>C
ENST00000436873.6:c.422A>C	ENSP00000398136.2:p.Tyr141Ser
ENST00000528571.5:c.*162A>C	ENSP00000434647.1:n.*162A>C
ENST00000530040.1:n.534A>C
ENST00000533371.5:c.-308A>C	ENSP00000437066.1:n.-308A>C
ENST00000534644.5:n.407A>C
ENST00000611494.4:c.422A>C	ENSP00000484546.1:p.Tyr141Ser
NM_000391.3:c.422A>C	NP_000382.3:p.Tyr141Ser
NM_000391.4:c.422A>C MANE Select	NP_000382.3:p.Tyr141Ser